Df(1)7aA: Deficiency (1) 7a from Austin
 cytology: Df(1)3C3-5;3C7-9; inferred from Mackensen's fig. 15F
  (1935).
 origin: X ray induced.
 references: Mackensen, 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Deficient for fa and spl but not w or ec; female N. Male lethal.
#
Df(1)14zA
 origin: X ray induced.
 discoverer: Mackensen.
 references: 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Deficient for f but not fw or r. Male lethal.
#
Df(1)24a
 origin: X ray induced.
 discoverer: Mackensen.
 references: 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Deficient for w but not pn or fa. Male lethal.
#
Df(1)60b
 origin: X ray induced.
 discoverer: Mackensen.
 references: 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Deficient for f but not fw or r. Male lethal.
#
Df(1)62d18
 cytology: Df(1)3B2-C1;C3-5 (Judd).
 origin: X ray induced.
 discoverer: Judd, 62d18.
 genetics: Deficient for l(1)zw6, l(1)zw7, and l(1)zw9
  but not l(1)zw3]. Lethal in male and in
  combination with all alleles of l(1)zw6 except
  l(1)zw6[l12]. Forms a viable heterozygote with
  In(1)w[m4L]rst[3R] =
  In(1)3C1-2;20A[L]3C3-4;20B[R] (deficiency for
  3C2-3), which is w rst in phenotype. This
  combination should be homozygous deficient for 3C3 and
  lethal [see l(1)3C3]; the discrepancy is unexplained.
#
Df(1)62g18
 origin: X ray induced.
 discoverer: Judd, 62g18.
 genetics: Deficient for z and l(1)zwl but not l(1)zw8. Male lethal.
#
Df(1)64c4
 cytology: Df(1)3A4-6;3C3-5 (Judd).
 origin: X ray induced.
 discoverer: Judd, 64c4.
 genetics: Deficient for all known lethal loci between z and w. Also deficient for w but not for z. Male lethal.
#
Df(1)64f1
 origin: X ray induced.
 discoverer: Abrahamson, 64f1.
 genetics: Deficient for l(1)zw3 and l(1)zw6 but not l(1)zw2 or l(1)zw7. Male lethal (Judd).
#
Df(1)64j4
 cytology: Df(1)3A6-8;3B1-2 (Judd) + Df(1)3B4-C2;3C1-4 (i.e., w[258-45]).
 origin: Spontaneous in w[258-45]-bearing X chromosome.
 discoverer: Judd, 64j4.
 genetics: Deficient for l(1)zw2 and l(1)zw3 but not l(1)zw4 or l(1)zw6. Male lethal.
#
Df(1)172
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for pn, w, fa, and ec. Male lethal.
#
Df(1)231c
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for v. Male lethal.
#
Df(1)235
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for pn, w, fa, and ec. Male lethal.
#
Df(1)244
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for m. Male lethal.
#
Df(1)247a
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for m. Male lethal.
#
Df(1)247g
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for w. Male lethal.
#
Df(1)260-1
 cytology: Df(1)1B4-6; apparently a terminal deficiency (Demerec and Hoover).
 origin: Spontaneous.
 discoverer: L. V. Morgan, 1932.
 synonym: Df(1)0-sc,LVM.
 references: Demerec and Hoover, 1936, J. Heredity 27: 206-12 (fig.).
 references: Sutton, 1943, Genetics 28: 213.
 genetics: Deficient for y, ac, and sc but not svr.
  Male lethal but not cell lethal (Ephrussi, 1934,
  Proc. Nat. Acad. Sci. U.S. 10: 420-22; Walen,
  1961, Genetics 46: 93-103).
#
Df(1)260-2
 cytology: Df(1)1B2-3; apparently a terminal deficiency (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 33k.
 references: Demerec and Hoover, 1936, J. Heredity 27: 206-12 (fig.). Sutton, 1943, Genetics 28: 211.
 genetics: Deficient for y and ac but not sc.
  Hemizygous lethal but not cell lethal. Embryo
  develops to fully-formed larva but fails to hatch
  (Kaliss, 1939, Genetics 24: 244-70).
#
Df(1)260-5
 cytology: Df(1)1A4-5; apparently a terminal deficiency (Demerec and Hoover).
 discoverer: Hoover, 1935.
 references: Demerec and Hoover, 1936, J. Heredity 27: 206-12 (fig.).
 references: Sutton, 1943, Genetics 28: 214.
 genetics: No phenotypic effect. Fertility and viability normal.
#
Df(1)260-10
 cytology: Df(1)1A2-3; apparently a terminal deficiency
  (Sutton).
 origin: X ray induced.
 discoverer: Sutton, 39a.
 references: 1940, Genetics 25: 628-35.
 genetics: Mutant for y and ac but not sc. Viable.
#
Df(1)260-19
 cytology: Df(1)1A2-3; apparently a terminal deficiency
  (Sutton).
 origin: Spontaneous.
 discoverer: Sutton, 1939.
 references: 1940, Genetics 25: 628-35. 1943, Genetics 28: 214.
 genetics: No phenotypic effects. Both sexes viable and fertile.
#
Df(1)262
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for fa; female N. Male lethal.
#
Df(1)267
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for fa; female N. Male lethal.
#
Df(1)268
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for car. Male lethal.
#
Df(1)271
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for fa; female N. Male lethal. Reduces crossing over.
#
Df(1)274
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for f. Male lethal.
#
Df(1)303
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for fa; female N. Male lethal.
#
Df(1)308
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for fa and ec. Male lethal.
#
Df(1)314
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
  Mackensen, 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Deficient for w, fa, and ec but not pn or bi. Male lethal.
#
Df(1)354
 origin: X ray induced.
 discoverer: Patterson.
 references: 1932, Am. Naturalist 66: 193-206.
 genetics: Deficient for pl. Male lethal.
#
Df(1)A1: Deficiency (1) from Austin
 cytology: Df(1)9B;20.
 origin: Aneuploid segregant from T(1;4)A1/+.
#
Df(1)A12
 cytology: Df(1)7A;7B.
 origin: Aneuploid segregant from T(1;2;4)A12/+.
#
Df(1)A124
 cytology: Df(1)10A;13A1-2.
 origin: Aneuploid segregant from T(1;2)A124/+.
#
Df(1)ac: Deficiency (1) achaete
 origin: X ray induced simultaneously with a detachment of an
  attached X.
 discoverer: Muller.
 references: 1954, DIS 28: 146-47.
 genetics: Deficient for ac and probably Y. Male
  viable.
#
Df(1)B[263-20]: Deficiency (1) Bar
 cytology: Df(1)15F9-16A1;16A6-B1 superimposed on
  Dp(1;1)15F9-16A1;16A7-B1.
 new order:: 1 - 15F9|16B1 - 20.
 origin: X ray induced in B chromosome.
 discoverer: Demerec, 34a.
 references: Sutton, 1943, Genetics 28: 97-107 (fig.).
 genetics: Reversion of B. Deficient for f but not
  os. Male lethal.
#
Df(1)bb: Deficiency (1) bobbed
 cytology: Df(1)20C;20D.
 origin: Associated with In(1)bb[Df].
#
Df(1)bb[G]: Deficiency (1) bobbed of Gershenson
 cytology: Df(1)19F-20C1;20B-D1.
 origin: Associated with In(1)sc[4L]sc[8R].
#
Df(1)bb[l-3a]: Deficiency (1) bobbed-lethal
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Deficient for bb. Segregates irregularly from
  y[+]Y in male. X/0 male lethal.
#
Df(1)bb[l-74]
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Deficient for bb. Segregates irregularly from
  y[+]Y in male. X/0 male lethal.
#
Df(1)bb[l-158]
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Deficient for bb. Segregates irregularly from
  y[+]Y in male. X/0 male lethal.
#
Df(1)bb[l-452]
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Deficient for bb. Segregates irregularly from
  y[+]Y in male. X/0 male lethal.
#
Df(1)bb[l-456]
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Deficient for bb. Segregates irregularly from
  y[+]Y in male. X/0 male lethal.
#
Df(1)bb[l-481]
 cytology: Also carries In(1)481 = In(1)12E-F;14B.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Deficient for bb. Segregates irregularly from
  y[+]Y in male. X/0 male lethal.
#
Df(1)bis: Deficiency (1) bistre
 cytology: Df(1)7B5-6;7B7-8.
 origin: Induced by
  DL-p-N,N-di-(2-chloroethyl)aminophenylalanine
  (CB. 3007).
 discoverer: Fahmy, 1954.
 references: 1958, DIS 32: 67.
 genetics: Deficient for bis. Male viable but sterile.
#
Df(1)C-PL Deficiency (1) C of Peterson and Laughnan
 cytology: Df(1)15F;16E.
 origin: Spontaneous; allegedly an asymmetrical exchange.
 discoverer: Peterson and Laughnan.
 references: 1963, Proc. Nat. Acad. Sci. U.S. 50: 126-33.
 genetics: Deficient for f and B but not os. Male
  lethal.
#
Df(1)Cl[L]bb[DfR]
 cytology: Df(1)4A5-B1;4D2-3 + Df(1)17A6-B1;20C-D.
 origin: Associated with In(1)C1[L]bb[DfR].
#
Df(1)Cl[L]y[4R]
 cytology: Df(1)17A6-B1;18A3-4.
 origin: Associated with In(1)C1[L]y[4R].
#
Df(1)cm[R8aH4]: Deficiency (1) carmine
 cytology: Df(1)6E.
 origin: X ray induced in R(1)2.
 discoverer: Muller, Valencia, and Valencia, 1946-53.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Deficient for cm.
#
Df(1)cmD5: Deficiency (1) carmine of De Frank
 cytology: Df(1)6E5-6;6F2-3.
 origin: X ray induced.
 discoverer: De Frank.
 genetics: Deficient for cm. Male lethal.
#
Df(1)cmH2: Deficiency (1) carmine of Hannah
 cytology: Df(1)6D8-E1;6E6-F1 (Hannah).
 origin: X ray induced.
 discoverer: Hannah.
 genetics: Deficient for cm. Male lethal.
#
Df(1)cmH4
 cytology: Df(1)6D8-E1;6E6-F1 (Hannah).
 origin: X ray induced.
 discoverer: Hannah.
 genetics: Deficient for cm. Male lethal.
#
Df(1)ct[2a2]: Deficiency (1) cut
 cytology: Df(1)7B3-6;7B6-7.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet., 8th., pp. 588-89.
 genetics: Deficient for ct but not cm, sn, or oc.
  Male lethal.
#
Df(1)ct[2a3]
 cytology: Df(2)7B2-3;7C1-2.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet., 8th., pp. 588-89.
 genetics: Deficient for ct but not cm, sn, or oc.
  Male lethal.
#
Df(1)ct[4b1]
 cytology: Df(1)7B2-4;7C2-4.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet., 8th., pp. 588-89.
 genetics: Deficient for ct but not cm, sn, or oc.
  Male lethal.
#
Df(1)ct[7a2]
 cytology: Df(1)7A5-B1;7C4-9.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet., 8th., pp. 588-89.
 genetics: Deficient for ct but not cm, scp, sn, or
  oc. Male lethal.
#
Df(1)ct[7c2]
 cytology: Df(1)6F11-7A1;7B8-C1.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet., 8th., pp. 588-89.
 genetics: Deficient for ct but not cm, scp, or sn.
  Male lethal.
#
Df(1)ct[10a1]
 cytology: Df(1)7B3-4;7B6-7 (questionable).
 origin: X ray induced.
 discoverer: De Frank, 1947.
 references: Hannah, 1949, Proc. Intern. Congr. Genet.,
  8th., pp. 588-89.
 genetics: Deficient for ct but not cm, scp, or sn.
  Male lethal.
#
Df(1)ct[10b1]
 cytology: Df(1)6D8-E1;7B7-C1.
 origin: X ray induced
 discoverer: Hannah, 1947.
 references: 1959, Proc. Intern. Congr. Genet.,
  8th., pp. 588-89.
 genetics: Deficient for ct but not cm or sn. 6E
  and F may be transposed rather than lost; otherwise,
  it should be deficient for cm. Male lethal.
#
Df(1)ct[12c2]
 origin: Df(1)7B2-3;7B6-7 (possibly).
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet.,
  8th., pp. 588-89.
 genetics: Deficient for ct but not cm, sn, or oc.
  Male lethal.
#
Df(1)ct[14b1]
 cytology: Df(1)7B2-3;7C3-4.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet.,
  8th., pp. 588-89.
 genetics: Deficient for ct but not cm, sn, or oc.
  Male lethal.
#
Df(1)ct[14c1]
 cytology: Df(1)7B3-4;7B6-9.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet.,
  8th., pp. 588-89.
 genetics: Deficient for ct but not cm, sn, or oc.
  Male lethal.
#
Df(1)ct[15b1]
 cytology: Df(1)7B2-4;7B6-7.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet.,
  8th., pp. 588-89.
 genetics: Deficient for ct but not cm, sn, or oc.
  Male lethal.
#
Df(1)ct[268-13]
 cytology: Df(1)2E3-F1;2F2-3 + Df(1)7B2-3;7B4-5 +
  Df(1)19A4-5;19A6-B1.
 origin: Associated with In(1)ct[268-13].
#
Df(1)ct[268-18]
 cytology: Df(1)7B2-3;7B4-5.
 origin: Associated with In(1)ct[268-18].
#
Df(1)ct[268-20]
 cytology: Df(1)6F11-7A1;7B5-6.
 origin: Associated with In(1)ct[268-20].
#
Df(1)ct[268-30]
 cytology: Df(1)7B2-3;7C3-4.
 origin: X ray induced.
 discoverer: Hoover, 38d.
 genetics: Deficient for ct but not scp or sn.
  Male lethal.
#
Df(1)ct[268-37]
 cytology: Df(1)5D2-3;7B2-3.
 origin: Aneuploid segregant from T(1;3)ct[268-37]/+.
#
Df(1)ct[268-42]
 cytology: Df(1)7A5-6;7B8-C1 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40a.
 genetics: Deficient for ct but not cm, scp, or sn.
  Male lethal.
#
Df(1)f[257-5]: Deficiency (1) forked
 cytology: Df(1)15E7-F1;15F2-4 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 33k.
 genetics: Deficient for f but not vb, r, or os.
  Male lethal and cell lethal.
#
Df(1)f[257-6]
 cytology: Df(1)15E4-F1;15F9-16A1;16A7-B1.
 new order:: 1 - 15E4|16A1 - 20.
 origin: X ray induced in Dp(1;1)B =
  Dp(1;1)15F9-16A1;16A7-B1.
 discoverer: Bridges, 1917.
 references: Sutton, 1943, Genetics 28: 97-107 (fig.).
 genetics: Reversion of B. Deficient for f but not
  vb, M(1)o, or os. Male lethal.
#
Df(1)f[257-9]
 cytology: Df(1)15E7-F1;16D2-4.
 origin: X ray induced.
 discoverer: Demerec, 34c.
 references: Sutton, 1943, Genetics 28: 97-107 (fig.).
 genetics: Deficient for f and B but not vb, un,
  lh, or os. Male lethal.
#
Df(1)f[257-27]
 cytology: Df(1)14F6-15A1;15F5-6.
 origin: X ray induced.
 discoverer: Demerec, 38l.
 genetics: Deficient for f and M(1)o but B not
  affected. Male lethal.
#
Df(1)f[257-28]
 cytology: Df(1)15E7-F1;16E5-F1.
 origin: X ray induced.
 discoverer: Sutton, 40h.
 genetics: Deficient for f and B regions. Male lethal.
#
Df(1)f[257-31]
 cytology: Df(1)15E7-F1;15F5-6.
 origin: X ray induced.
 discoverer: Bishop, 41a.
 genetics: Deficient for f but not M(1)o or os.
  Male lethal.
#
Df(1)g[l]: Deficiency (1) garnet-lethal
 cytology: Df(1)12A;12E (Nicoletti).
 origin: Spontaneous.
 discoverer: L. V. Morgan, 24l24.
 genetics: Deficient for g and ty but not wy, s, pl,
  or sd. Lethal in male and cell lethal.
#
Df(1)lz1: Deficiency (1) lozenge
 cytology: Df(1)7E11-F1;8E1-2 (Hannah).
 origin: X ray induced.
 discoverer: Green.
 references: Green and Green, 1956, Z. Indukt. Abstamm. Vererbungsl. 87: 708-21.
 genetics: Deficient for lz and amx. Male lethal.
#
Df(1)lz2
 cytology: Df(1)8C14-D2;8E3-4 (Hannah).
 origin: X ray induced.
 discoverer: Green.
 references: Green and Green, 1956, Z. Indukt. Abstamm. Vererbungsl. 87: 708-21.
 genetics: Deficient for lz and amx. Male lethal.
#
Df(1)lz3
 cytology: Df(1)8C1-3;8D12-E2 (Hannah).
 origin: X ray induced.
 discoverer: Green.
 references: Green and Green, 1956, Z. Indukt. Abstamm. Vererbungsl. 87: 708-21.
 genetics: Deficient for lz and amx. Male lethal.
#
Df(1)lz5
 cytology: Df(1)8D3-5;8F-9A (Hannah).
 origin: X ray induced.
 discoverer: Green.
 references: Green and Green, 1956, Z. Indukt. Abstamm. Vererbungsl. 87: 708-21.
 genetics: Deficient for lz and amx. Male lethal.
#
Df(1)lzA
 cytology: Df(1)3E;3F + Df(1)9E;9F-10A.
 origin: Associated with In(1)lzA.
#
Df(1)m[259-4]: Deficiency (1) miniature
 cytology: Df(1)10C2-3;10E2-3.
 origin: X ray induced.
 discoverer: Demerec, 33i.
 references: Dorn and Burdick, 1962, Genetics 47: 503-18.
 genetics: Male lethal. Heterozygote with m mutations has
  m phenotype. Heterozygote with dy mutations
  is wild type. Recombines with m[59], m, m[D],
  dy[61a], dy, and dy[58k].
  1980).
#
Df(1)M-30: Deficiency (1) Minute-30.
 origin: Spontaneous.
 discoverer: Schultz.
 references: 1929, Genetics 14: 366-419.
 genetics: Deficient for cv and M(1)30. Male lethal.
#
Df(1)mal: Deficiency (1) maroonlike
 origin: X ray induced in In(1)sc[8].
 discoverer: E. H. Grell.
 references: 1962, Z. Indukt. Abstamm. Vererbungsl. 93: 371-77.
 genetics: Deficient for sw, mal, and su(f) but not
  car or M(1)n. Male lethal.
#
Df(1)N[8]: Deficiency (1) Notch
 cytology: Df(1)3B4-C1;3D6-E1.
 origin: Spontaneous.
 discoverer: Mohr, 18j7.
 references: 1919, Genetics 4: 275-82.
  1932, Proc. Intern. Congr. Genet., 6th., Vol. 1: 202.
  Slizynska, 1938, Genetics 23: 291-99 (fig.).
 genetics: Deficient for w, rst, fa, spl, and dm.
  Male lethal.
#
Df(1)N[25]
 origin: Spontaneous.
 discoverer: Mohr, 28k22.
 genetics: Not deficient for w. Male lethal.
#
Df(1)N[26]
 cytology: Df(1)3C4-5;3C8-9 (Sutton).
 origin: Spontaneous.
 discoverer: Mohr, 28k29.
 genetics: Deficient for fa and spl but not w, rst,
  or dm. Male lethal.
#
Df(1)N[29]
 origin: Spontaneous.
 discoverer: Eker, 36e12.
 genetics: Deficient for w. Male lethal.
#
Df(1)N[33h]
 cytology: Df(1)3C6-7;3D2-3 (Sutton).
 origin: Spontaneous.
 discoverer: Ives, 33h29.
 references: Plough and Ives, 1934, DIS 1: 31.
  1934, DIS 2: 10, 34.
  Demerec, 1941, Proc. Intern. Congr. Genet., 7th.,
  pp. 99-103.
 genetics: Deficient for fa but not pn, w, or ec.
  Male lethal.
#
Df(1)N[38g]
 cytology: Df(1)3C4-5;3C7-8 (Sutton).
 origin: Spontaneous.
 discoverer: Curry, 38g.
 genetics: Deficient for fa and spl but not w, rst,
  or dm. Male lethal.
#
Df(1)N[63b]
 cytology: Df(1)3C2-3;3E2-3.
 origin: X ray induced.
 references: Lefevre and Wilkins, 1966, Genetics 53: 175-87.
 genetics: Deficient for N.
  Carries w[63b], a white
  allele causing marbled pigmentation of the eyes.
  Df(1)N[63b]/w resembles w[sp]/w.
  Df(1)N[63b]/Df(1)w[258-45] survives and has
  lighter eye color than w[sp]/Df(1)w[258-45].
#
Df(1)N[264-2]
 cytology: Df(1)3C6-7;3C7-8.
 origin: X ray induced.
 discoverer: Demerec, 33j.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Deficient for spl and fa but not w, rst,
  or ec. Male lethal.
#
Df(1)N[264-7]
 cytology: Df(1)3C6-7;3C8-9.
 origin: Associated with In(1)N[264-7].
#
Df(1)N[264-13]
 cytology: Df(1)3C6-7;3C10-11 (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 34A.
 genetics: Deficient for fa, spl, and fa[n] but not
  w, rst, dm, or ec. Male lethal.
#
Df(1)N[264-15]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 34c.
 genetics: Deficient for fa and spl but not w.
  Male lethal.
#
Df(1)N[264-19]
 cytology: Df(1)3C6-7;3C7-8.
 origin: X ray induced.
 discoverer: Demerec, 34k.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Deficient for fa but not w or ec. Male
  lethal.
#
Df(1)N[264-30]
 cytology: Df(1)3A4-5;3C7-9.
 origin: X ray induced.
 discoverer: Demerec, 36d.
 references: Slizynska, 1938, Genetics 23: 291-99 (fig.).
 genetics: Deficient for w, rst, and fa but not pn,
  kz, or dm. Male lethal.
#
Df(1)N[264-31]
 cytology: Df(1)3B4-C1;3D1-3.
 origin: X ray induced.
 discoverer: Demerec, 36d.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Deficient for w, rst, fa, and dm but not
  pn or ec. Male lethal.
#
Df(1)N[264-32]
 cytology: Df(1)3C3-5;3C7-8.
 origin: X ray induced.
 discoverer: Demerec, 36h.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Deficient for rst and fa but not w or
  dm. Male lethal.
#
Df(1)N[264-33]
 cytology: Df(1)3C6-7;3C7-8.
 origin: X ray induced.
 discoverer: Hoover, 36h.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Deficient for fa but not rst or dm.
  Male lethal.
#
Df(1)N[264-36]
 cytology: Df(1)3A3-4;3D2-3.
 origin: X ray induced.
 discoverer: Demerec, 37b.
 references: Slizynska, 1938, Genetics 23: 291-99 (fig.).
 genetics: Deficient for w, rst, fa, and dm. Male
  lethal.
#
Df(1)N[264-37]
 cytology: Df(1)3C6-7;3C7-8.
 origin: X ray induced.
 discoverer: Demerec, 37b.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Deficient for fa but not w, rst, or dm.
  Male lethal.
#
Df(1)N[264-38]
 cytology: Df(1)2D3-4;3E2-3.
 origin: X ray induced.
 discoverer: Demerec, 37b.
 references: Slizynska, 1938, Genetics 23: 291-99 (fig.).
 genetics: Deficient for pn, kz, w, rst, fa, and dm but
  not br, M(1)3E, or ec. Male lethal.
#
Df(1)N[264-39]
 cytology: Df(1)3C6-7;3C7-8 (Slizynska, 1938, Genetics
  23: 291-99; Welshons, 1959,
  Proc. Nat. Acad. Sci. U.S. 44: 254-58).
  Recent re-examination of chromosomes
  in males from lines marked N[264-39] reveals
  presence of 3C7 (Welshons).
 origin: Spontaneous.
 discoverer: Slizynska, 1937.
 genetics: Deficient for fa. Male lethal.
#
Df(1)N[264-41]
 cytology: Df(1)3C6-7;3C8-9 (Sutton).
 origin: Spontaneous.
 discoverer: Slizynska, 37e.
 genetics: Deficient for fa but not rst or dm. Male
  lethal.
#
Df(1)N[264-42]
 cytology: Df(1)3C4-5;4B4-6 (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 37e.
 genetics: Deficient for fa, dm, and ec but not w,
  rst, or bi. Male lethal.
#
Df(1)N[264-46]
 discoverer: Df(1)3C6-7;3C7-8.
 origin: X ray induced.
 cytology: Demerec, 37f.
 genetics: Deficient for fa but not w, rst, or dm.
  Male lethal.
#
Df(1)N[264-48]
 cytology: Df(1)1B6-7;1B10-11.
 origin: Associated with In(1)N[264-48].
#
Df(1)N[264-49]
 cytology: Df(1)3C4-5;3E8-F1 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 37j.
 genetics: Deficient for fa, dm, and M(1)3E but not
  w, rst, ec, or bi. Male lethal.
#
Df(1)N[264-51]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: Found among progeny of radium-treated male.
 discoverer: Demerec, 37k.
 genetics: Deficient for fa but not w, rst, or dm.
  Male lethal.
#
Df(1)N[264-54]
 cytology: Df(1)3C3-5;3C7-8 (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 38b.
 genetics: Deficient for fa but not w, rst, or dm.
  Male lethal.
#
Df(1)N[264-58]
 cytology: Df(1)3B2-3;3D6-7.
 origin: Aneuploid segregant from T(1;3)N[264-58]/+.
#
Df(1)N[264-68]
 cytology: Df(1)3A10-B1;3E8-F1 (Demerec).
 origin: X ray induced.
 discoverer: Demerec, 38k.
 genetics: Deficient for w, rst, dm, and M(1)3E but not
  pn, kz, or ec. Male lethal.
#
Df(1)N[264-72]
 cytology: Df(1)3C6-7;3C7-9 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 38k.
 genetics: Deficient for fa but not rst or dm.
  Male lethal.
#
Df(1)N[264-73]
 cytology: Df(1)3C3-4;4C6-7 (Demerec).
 origin: X ray induced.
 discoverer: Demerec, 38l.
 genetics: Deficient for fa, rst, dm, M(1)3E, ec, and
  M(1)4BC but not w, bi, or rb. Male
  lethal.
#
Df(1)N[264-76]
 cytology: Df(1)3B4-C1;3E4-5 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39b.
 genetics: Deficient for w, rst, fa, dm, and M(1)3E but
  not pn or ec. Male lethal.
#
Df(1)N[264-77]
 cytology: Df(1)3B4-C1;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39b.
 genetics: Deficient for w, fa, and dm but not pn
  or ec. Male lethal.
 genetics: Right break disagrees with inclusion of dm.
  Either breakpoint is farther to the right or dm
  is mutant instead of missing.
#
Df(1)N[264-79]
 cytology: Df(1)2C10-D1;3C6-7 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39c.
 genetics: Weak Notch phenotype; fa is affected. Deficient
  for kz, pn, w, and rst but not br or
  dm. Male lethal.
#
Df(1)N[264-81]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39d.
 genetics: Deficient for fa but not rst or dm.
  Male lethal.
#
Df(1)N[264-86]
 cytology: Df(1)3C7-8;3E5-6.
 origin: Aneuploid segregant from T(1;4)N[264-86]/+.
#
Df(1)N[264-89]
 cytology: Df(1)3B2-3;3F2-3 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39j.
 genetics: Deficient for w, rst, fa, M(1)3E, and ec but
  not pn. Male lethal.
#
Df(1)N[264-90]
 cytology: Df(1)3C7-8;3E8-F1 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39j.
 genetics: Deficient for spl, dm, M(1)3E, and ec but not
  pn or w. Male lethal.
#
Df(1)N[264-93]
 cytology: Df(1)3B4-C1;3F3-4 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39k.
 genetics: Deficient for w, spl, dm, M(1)3E, and ec but
  not pn or bi. Male lethal.
#
Df(2)N[264-96]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39k.
 genetics: Deficient for spl but not w, rst, dm, or
  ec. Male lethal.
#
Df(1)N[264-99]
 cytology: Df(1)2D2-3;3C11-12 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40a.
 genetics: Deficient for pn, kz, w, rst, spl, and dm but
  not ec or bi. Male lethal.
#
Df(1)N[264-100]
 cytology: Df(1)3B4-C1;4B4-5.
 origin: Aneuploid segregant from T(1;3)N[264-100]/+.
#
Df(1)N[264-101]
 cytology: Df(1)3C4-5;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40a.
 genetics: Deficient for spl but not w, rst, or dm.
  Male lethal.
#
Df(1)N[264-105]
 cytology: Df(1)3C6-7;3D2-3 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40a.
 genetics: Deficient for spl, and dm
  but not w, rst,
  or ec. Male lethal.
#
Df(1)N[264-106]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40a.
 genetics: Deficient for spl but not pn, w, rst, or
  dm. Male lethal.
#
Df(1)N[264-108]
 cytology: Df(1)3C3-5;3E7-8.
 origin: Associated with In(1)N[264-108].
#
Df(1)N[264-110]
 cytology: Df(1)3B4-C1;3D2-3 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40a.
 genetics: Deficient for w, rst, spl, and dm but not
  pn or ec. Male lethal.
#
Df(1)N[264-111]
 cytology: Df(1)3C3-5;3C12-D1 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40b.
 genetics: Deficient for spl and rst but not pn, w,
  dm, or ec. Male lethal.
#
Df(1)N[264-114]
 cytology: Df(1)3C6-7;3D4-5 (Sutton).
 origin: Spontaneous.
 discoverer: Kaufmann, 40d.
 genetics: Deficient for rst, spl, and dm but not w
  or ec. Male lethal.
#
Df(1)N[264-115]
 cytology: Df(1)3C3-5;3E2-3 (Sutton).
 origin: X ray induced.
 discoverer: Sutton, 40e.
 genetics: Deficient for rst, spl, and dm but not w,
  M(1)3E, or ec. Male lethal.
#
Df(1)N[264-117]
 cytology: Df(1)3A6-7;3E2-3 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40g.
 genetics: Deficient for w, rst, spl, and dm but not
  pn, ec, or bi. Male lethal.
#
Df(1)N[264-118]
 cytology: Df(1)3C6-7;3C7-9 (Sutton).
 origin: Spontaneous.
 discoverer: Demerec, 40h.
 genetics: Deficient for spl but not pn, w, rst, or
  dm. Male lethal.
#
Df(1)N[264-120]
 cytology: Df(1)3C6-7;3D2-3 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40j.
 genetics: Deficient for spl and dm but not kz, w,
  rst, or ec. Male lethal.
#
Df(1)N[264-125]
 cytology: Df(1)3C4-5;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 41a.
 genetics: Deficient for spl but not kz, w, rst, dm, or
  ec. Male lethal.
#
Df(1)N[264-126]
 cytology: Df(1)3C3-5;3D4-5 (Sutton).
 origin: Spontaneous.
 discoverer: Bishop, 40l.
 genetics: Deficient for rst, spl and dm but not w.
  Male lethal.
#
Df(1)N[264-127]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 41b.
 genetics: Deficient for spl but not kz, w, rst, or
  dm. Male lethal.
#
Df(1)N[264-128]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 41b.
 genetics: Deficient for spl but not w, rst, or dm.
  Male lethal.
#
Df(1)N[264-130]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: Spontaneous.
 discoverer: Neel, 41c.
 references: 1942, Genetics 27: 530.
 genetics: Deficient for fa but not w, rst, or dm.
  Male lethal.
#
Df(1)N[B]: Deficiency (1) Notch of Bernstein
 cytology: Df(1)3C4-5;3C12-D1 (Sutton).
 origin: Spontaneous.
 discoverer: Bernstein, 28a7.
 genetics: Deficient for fa but not w, rst, or dm.
  Male lethal.
#
Df(1)N[EZ]
 cytology: Df(1)3C6-7;3C7-8 (Sutton).
 origin: Spontaneous.
 discoverer: Morgan, 1929.
 genetics: Deficient for fa but not w Male lethal.
#
Df(1)O4: Deficiency (1) of Oliver
 origin: Aneuploid segregant from T(1;3)O4/+.
#
Df(1)pn[l10Ac4]: Deficiency (1) prune
 cytology: Df(1)2C8-9;3A1-2 superimposed on
  In(1)1B3-4;20B-D1[L]1B2-3;20B-D1[R] +
  In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B3|20B - 11F4|4E1 -
  11F2|4D7 - 3A2|2C8 - 1B3|20D1 -
  20F.
 origin: X ray induced in In(1)sc[S1L]sc[8R]+dl-49.
 discoverer: Muller, Valencia, and Valencia, 1946-53.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Deficient for pn.
#
Df(1)pn-ec: Deficiency (1) prune to echinus
 cytology: Df(1)2D1-2;3F7-4A4.
 origin: Aneuploid segregant from T(1;A)pn-ec/+.
#
Df(1)ras-v[17Cc8] Deficiency (1) raspberry to vermilion
 cytology: Df(1)9E3-4;10A4-5 superimposed on
  In(1)1B3-4;20B-D1[L]1B2-3;20B-D1[R] +
  In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B3|20B - 11F4|4E1 - 9E3|10A5
  - 11F2|4D7 - 1B3|20D1 - 20F.
 origin: X ray induced in In(1)sc[S1L]sc[8R]+dl-49.
 discoverer: Muller, Valencia, and Valencia, 1946-53.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Deficient for ras and v.
#
Df(1)rb[R15BH3]: Deficiency (1) ruby
 cytology: Df(1)4B4-5;4D5-6.
 origin: X ray induced in R(1)2.
 discoverer: Muller, Valencia, and Valencia, 1946-53.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Deficient for rb.
#
Df(1)rst[2]: Deficiency (1) roughest
 cytology: Df(1)3C3-4;3C6-7 (Schultz; Sutton).
 origin: Spontaneous.
 discoverer: Bridges, 33d7.
 references: Gersh, 1965, Genetics 51: 477-80 (fig.).
 genetics: Deficient for rst and vt. Homozygous
  viable.
#
Df(1)sc[4L]sc[8R]
 cytology: Df(1)19F-20C1;20B-D1 + Dp(1;1)1B2-3;11B3-4.
 origin: Associated with In(1)sc[4L]sc[8R].
#
Df(1)sc[4L]sc[L8R]
 cytology: Df(1)19F-20C1;20B-C.
 origin: Associated with In(1)sc[4L]sc[L8R].
#
Df(1)sc[8]: Deficiency (1) scute
 origin: Spontaneous in In(1)sc[8].
 discoverer: Noujdin.
 references: 1935, Zool. Zh. 14: 317-52.
 genetics: Deficient for y, ac, and Hw. Male lethal,
  dies as late embryo; larva nearly complete (Poulson,
  1940, J. Expt. Zool. 83: 271-325).
#
Df(1)sc[8]25b
 cytology: Like In(1)sc[8] in mitotic prophase but
  without heterochromatic segments hB and most of
  hA, which are ordinarily carried distally in
  In(1)sc[8].
 origin: Spontaneous derivative of In(1)sc[8]; Y
  chromosome not demonstrably involved.
 discoverer: Lindsley, 1952.
 synonym: sc[8]c.o. X 25b.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient for y and ac; mutant for bb.
  Male lethal with normal Y, viable with
  y[+]Y.
#
Df(1)sc[8]89a
 cytology: Like In(1)sc[8] in mitotic prophase.
 origin: Spontaneous product of recombination between the
  distal heterochromatin of In(1)sc[8] and
  Y[S].
 discoverer: Lindsley, 1952.
 synonym: sc[8]c.o. X 89a.
 references: 1955, Genetics 40: 24-44.
 genetics: Deficient for y and ac but not bb.
  Carries KS, the fertility complex of Y[S],
  distally. Male lethal with normal Y, viable with
  y[+]Y.
 genetics: Four similar deficiencies (Df(1)sc[8]Ed1u,
  Df(1)sc[8]Pd0u, Df(1)sc[8]91b, and
  Df(1)sc[8]67h) also described by Lindsley
  (1955).
#
Df(1)sc[8]99c
 cytology: Like In(1)sc[8] in mitotic prophase.
 origin: Spontaneous derivative of In(1)sc[8]; Y
  chromosome not demonstrably involved.
 discoverer: Lindsley, 1952.
 synonym: sc[8]c.o. X 99c.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient for y and ac but not for bb.
  Male lethal with normal Y, viable with
  y[+]Y.
#
Df(1)sc[8]B1
 cytology: Like In(1)sc[8L]EN[R] in mitotic prophase
  but with the part of heterochromatic segment hA
  ordinarily carried distally and a portion of hB
  missing.
 origin: Spontaneous derivative of
  In(1)sc[8L]EN[R]; Y chromosome not
  demonstrably involved. Postulated to result from
  exchange between the distal heterochromatin of
  one chromatid and the proximal heterochromatin of
  its sister.
 discoverer: Lindsley, 1950.
 synonym: sc[8]ENc.o X B1.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient distally for y and ac. Male
  viable.
 genetics: Two similar deficiencies (Df(1)sc[8]C6 and
  Df(1)sc[8]D8) described (Lindsley, 1958).
#
Df(1)sc[8]C4
 cytology: Like In(1)sc[8L]EN[R] in mitotic prophase.
 origin: Spontaneous derivative of
  In(1)sc[8L]EN[R]; Y chromosome not
  demonstrably involved. Postulated to result from
  exchange between the distal heterochromatin of
  one chromatid and the proximal heterochromatin of
  its sister.
 discoverer: Lindsley, 1950.
 synonym: sc[8]ENc.o X C4.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient distally for y and ac. Male
  viable.
 genetics: Five similar deficiencies (Df(1)sc[8]C13,
  Df(1)sc[8]D6, Df(1)sc[8]F7, Df(1)sc[8]O7, and
  Df(1)sc[8]53c) also described (Lindsley, 1958).
#
Df(1)sc[8]J3
 cytology: Like In(1)sc[8L]EN[R] in mitotic prophase
  but with the part of heterochromatic segment hA
  ordinarily carried distally and a portion of hB
  missing.
 origin: Spontaneous derivative of
  In(1)sc[8L]EN[R]; Y chromosome not
  demonstrably involved. Postulated to result from exchange
  between distal and proximal heterochromatin of
  sister chromatids.
 discoverer: Lindsley, 1950.
 synonym: sc[8]ENc.o X J3.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient distally for y and ac;
  mutant for bb. Male viable.
#
Df(1)sc[8]K1
 cytology: Like In(1)sc[8L]EN[R] in mitotic prophase
  but carries only heterochromatic segments hC
  and hD distally.
 origin: Spontaneous derivative of
  In(1)sc[8L]EN[R]; Y chromosome not
  demonstrably involved. Postulated to result from
  exchange between distal and proximal heterochromatin of
  sister chromatids.
 discoverer: Lindsley, 1950.
 synonym: sc[8]ENc.o X K1.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient distally for y and ac;
  mutant for bb. Male viable.
#
Df(1)sc[8]M
 origin: Spontaneous in In(1)sc[8].
 discoverer: Mather, 1937.
 genetics: Deficient for y, ac, and bb. Male lethal.
#
Df(1)sc[8]P7
 cytology: Like In(1)sc[8L]EN[R] in mitotic prophase.
 origin: Spontaneous product of recombination between the
  distal heterochromatin of In(1)sc[8L]EN[R]
  and Y[S].
 discoverer: Lindsley, 1950.
 synonym: sc[8]ENc.o. X P7.
 references: 1955, Genetics 40: 24-44.
 genetics: Deficient distally for y and ac but not
  bb. Carries KS, the fertility complex of
  Y[S], distally. Male viable.
 genetics: Three similar deficiencies (Df(1)sc[8]L7,
  Df(1)sc[8]P0, and
  Df(1)sc[8]35a) also
  described by Lindsley (1955).
#
Df(1)sc[8]Q1
 cytology: Like In(1)sc[8L]EN[R] in mitotic prophase
  but the portion of heterochromatic segment hA
  ordinarily carried distally missing.
 origin: Spontaneous derivative of
  In(1)sc[8L]EN[R]; Y chromosome not
  demonstrably involved. Postulated to result from
  exchange between distal and proximal heterochromatin
  of sister chromatids.
 discoverer: Lindsley, 1950.
 synonym: sc[8]ENc.o. X Q1.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient distally for y and ac. Male
  viable.
#
Df(1)sc[8]S7
 cytology: Like In(1)sc[8L]EN[R] in mitotic prophase
  but carries only heterochromatic segments hC and
  hD distally.
 origin: Spontaneous derivative of
  In(1)sc[8L]EN[R]; Y chromosome not
  demonstrably involved. Postulated to result from
  exchange between distal and proximal heterochromatin
  of sister chromatids.
 discoverer: Lindsley, 1950.
 synonym: sc[8]ENc.o. X S7.
 references: 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22.
 genetics: Deficient distally for y, ac, and bb. Male
  viable.
 genetics: A similar deficiency (Df(1)sc[8]W0) also
  described (Lindsley, 1958).
#
Df(1)sc[8L]sc[4R]
 cytology: Df(1)1B2-3;1B3-4.
 origin: Associated with In(1)sc[8L]sc[4R.
#
Df(1)sc[8L]sc[L8R]
 cytology: Df(1)1B2-3;1B3-4.
 origin: Associated with In(1)sc[8L]sc[L8R].
#
Df(1)sc[8L]sc[S1R]
 cytology: Df(1)1B2-3;1B3-4.
 origin: Associated with In(1)sc[8L]sc[S1R].
#
Df(1)sc[10-1]
 cytology: Df(1)1B1-2;1B2-3;1B14-C1.
 new order:: 1A - 1B1|1B14 - 1B3|1C1 - 20;
  1B2 missing.
 origin: X-ray-induced derivative of In(1)ac[3] =
  In(1)1B2-3;1B14-C1.
 discoverer: Sturtevant, 1930.
 references: 1935, DIS 3: 15.
  1936, Genetics 21: 444-66.
 genetics: Mutant for sc; viability low.
#
Df(1)sc[15]
 origin: X ray induced.
 discoverer: Muller.
 references: Patterson and Muller, 1930, Genetics 15: 495-577.
  Dubinin, 1933, J. Genet. 27: 443-64.
 genetics: Mutant for sc; deficient for y and ac.
  Apparently, y[+] and ac[+] loci were
  inserted into an autosome and subsequently lost.
  Originally tested as an allele of sc only. Male
  lethal.
#
Df(1)sc[19]
 cytology: Df(1)1B1-2;1B4-7.
 origin: Aneuploid segregant from T(1;2)sc[19]/+.
#
Df(1)sc[260-25]
 cytology: Df(1)1B2-3; terminal deficiency.
 origin: Aneuploid recombinant from In(1LR)sc[260-25]/+.
#
Df(1)sc[Fah]: Deficiency (1) scute of Fahmy
 cytology: Df(1)1A8-B1;1B2-3.
 origin: Induced by
  DL-p-N,N-di-(2-chloroethyl)aminophenylalanine
  (CB. 3007).
 discoverer: Fahmy, 1954.
 references: 1958, DIS 32: 74.
 genetics: Probably mutant for sc. Male viable; homozygous
  female lethal.
#
Df(1)sc[J4] Deficiency (1) scute of Jacobs-Muller
 cytology: Df(1)1B;3A3-C2.
 origin: Associated with T(1;3)sc[J4].
#
Df(1)sc[L8L]sc[8R]
 cytology: Df(1)20B-C;20B-D1.
 origin: Associated with In(1)sc[L8L]sc[8R].
#
Df(1)sc[L8L]sc[S1R]
 cytology: Df(1)20B-C;20B-D1.
 origin: Associated with In(1)sc[L8L]sc[S1R].
#
Df(1)sc[V1]: Deficiency (1) scute of Valencia
 cytology: Df(1)1A8-C3; terminal deficiency.
 origin: Aneuploid recombinant from In(1LR)sc[V1]/+.
#
Df(1)sn: Deficiency (1) singed
 cytology: Df(1)7B2-3;7D22-E1.
 origin: Spontaneous in R(1)2.
 discoverer: C. Hinton.
 references: Hinton and Welshons, 1955, DIS 29: 125-26.
 genetics: Deficient for sn but not ct, oc, or ptg.
  Male lethal.
#
Df(1)sta: Deficiency (1) stubarista
 cytology: Df(1)1D3-E1;2A.
 origin: Aneuploid segregant for T(1;3)sta/+.
#
Df(1)svr: Deficiency (1) silver
 cytology: Df(1)2B10-13; apparently a terminal
  deficiency.
 origin: Found among progeny of cold-treated female.
 discoverer: L. V. Morgan.
 references: 1940, DIS 13: 51.
  Sutton, 1943, Genetics 28: 213.
 genetics: Deficient for y, ac, sc, and svr but not
  su(s) or sta. Male lethal.
#
Df(1)t[282-1]: Deficiency (1) tan
 cytology: Df(1)8C2-3;8C14-D1 (Sutton). Green and Green
  (1956, Z. Indukt. Abstamm. Vererbungsl. 87: 708-21)
  suggested that the deficiency probably
  extends farther to the right.
 origin: X ray induced.
 discoverer: Demerec, 34c.
 genetics: Deficiency for t, lz, and amx but not dd,
  dvr, flp, ny, or ras. Male lethal.
#
Df(1)vB: Deficiency (1) vermilion of Bridges
 origin: Spontaneous.
 discoverer: Bridges, 16e9.
 references: 1919, J. Gen. Physiol. 1: 645-56.
 genetics: Deficient for v. Male lethal. Genetic map
  shortened 1-3 units.
#
Df(1)w[258-3]: Deficiency (1) white
 cytology: Df(1)3B2-3;3C1-2 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 33h.
 genetics: Claimed to have pn affected, but cytology is not in
  agreement with deficiency for pn; therefore,
  probably an independent mutant. w affected,
  probably mutant. br and fa not affected.
  Male lethal.
#
Df(1)w[258-11]
 cytology: Df(1)3A2-3;3C3-5.
 origin: X ray induced.
 discoverer: Demerec, 33j.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Deficient for w but not pn, kz, rst, fa, or
  ec. Male lethal.
#
Df(1)w[258-14]
 cytology: Df(1)3A3-4;3C1-2.
 discoverer: Demerec, 33k.
 references: Slizynska, 1938, Genetics 23: 291-99.
 genetics: Mutant or deficient for w but not pn, kz,
  rst, or fa. Male lethal.
#
Df(1)w[258-42]
 cytology: Df(1)3A6-8;3C3-5.
 origin: X ray induced.
 discoverer: Demerec, 38i.
 genetics: Deficient for w, but not pn, kz, or
  rst. Male lethal.
#
Df(1)w[258-45]
 cytology: According to Sutton, Df(1)3B4-C2;3C1-4 is
  Df(1)3B4-C1;3C1-2 but, according to Schultz,
  is Df(1)3C1-2;3C3-4. May lack 3C2 (Lefevre
  and Wilkins, 1964, Genetics 50: 264).
 origin: X ray induced.
 discoverer: Demerec, 38l.
 genetics: Mutant or deficient for w but not pn, kz,
  rst, or fa. Male lethal. Lethal phase in
  embryo.
#
Df(1)w[258-48]
 cytology: Df(1)3A9-B1;3C1-2 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39c.
 genetics: Mutant or deficient for w but not pn, kz,
  rst, or fa. Male lethal.
#
Df(1)w[m4L]rst[3R]
 cytology: Df(1)3C1-2;3C3-4 + Df(1)20A;20B.
 origin: Associated with In(1)w[m4L]rst[3R].
#
Df(1)w[m4L]w[mJR]
 cytology: Df(1)3C1-2;3C2-3 + Df(1)20.
 origin: Associated with In(1)w[m4L]w[mJR].
#
Df(1)w[m49a]: Deficiency (1) white-mottled
 cytology: Df(1)3A10-B1;3E2-3.
 origin: Aneuploid segregant from T(1;3)w[m49a]/+.
#
Df(1)w[m53a]
 cytology: Df(1)3B2-C1;3C9-D1.
 origin: Aneuploid segregant from T(1;2)w[m53a]/+.
#
Df(1)w[m258-44]
 cytology: Df(1)3C3-4;4D2-E1.
 origin: Aneuploid segregant from T(1;2;3)w[m258-44]/+.
#
Df(1)w[mDV4] Deficiency (1) white-mottled of Dubinin and Volotov
 cytology: Df(1)3C3-7;3D.
 origin: Associated with T(1;4)w[mDV4].
#
Df(1)w[mJL]rst[3R]
 cytology: Df(1)3C2-3;3C3-4.
 origin: Associated with In(1)w[mJL]rst[3R].
#
Df(1)w[rG] Deficiency (1) white-recombinant of Green
 cytology: Df(1)3A3-4;3C1-2 (E. B. Lewis).
 origin: A regular product of unequal exchange between 3C1-2 of a
  w[a] or w[a2] chromosome and 3A3-4 of certain
  specific homologous chromosomes. Reciprocal of
  Dp(1;1)w[rG].
 discoverer: Green.
 references: 1959, Genetics 44: 1243-56.
 genetics: Mutant or deficient for w but not z. Male
  lethal. Survives as w female when heterozygous with
  Df(1)w[m4L]rst[3R] = Df(1)3C1-2;3C3-4.
#
Df(1)w[rJ1] Deficiency (1) white-recombinant of Judd
 cytology: Df(1)3A2-3;3C1-2.
 origin: A regular product of unequal exchange between the 3C1-3
  region of a chromosome carrying w[a] and the 3A2-3
  region of certain specific homologous chromosomes.
 discoverer: Judd.
 synonym: w[-].
 references: 1961, Genetics 46: 1687-97 (fig.).
  1964, DIS 39: 60.
 genetics: Deficient for z and the lethals
  between z and
  w; mutant or deficient for w. Male lethal.
  Survives as a w female when heterozygous for the
  deficiency for 3C2-3, Df(1)w[m4L]rst[3R] =
  Df(1)3C1-2;3C3-4.
#
Df(1)w[rJ2]
 cytology: Df(1)3A6-8;3C1-3 [could be the same as
  Df(1)w[rG]].
 origin: A regular product of unequal exchange between the 3C1-3
  region of a chromosome carrying w[a]
  or w[rdp] with the 3A4-8 region
  of specific homologous chromosomes.
  Probably reciprocal recombinant of Dp(1;1)w[rJ2].
 discoverer: Judd.
 synonym: w[-].
 references: 1961, Genetics 46: 1687-97 (fig.).
  1964, DIS 39: 59.
 genetics: Carries normal alleles of z, l(1)zwl, l(1)zw8, and
  l(1)zw4; deficient for the other l(1)zw's;
  mutant or deficient for w. Male lethal. Survives as
  w female when heterozygous with the deficiency for
  3C2-3, Df(1)w[m4L]rst[3R] = Df(1)3C1-2;3C3-4.
#
Df(1)w[rJ3]
 cytology: Df(1)3C1-3;3C12-D3.
 origin: Product of unequal exchange between the 3C1-3 region of a
  chromosome carrying w[a] and region 3C12-D3 of a
  specific homolog.
 discoverer: Judd.
 synonym: w[-r] N.
 references: 1961, Genetics 46: 1687-97 (fig.).
  1964, DIS 39: 59.
 genetics: Deficient for N; mutant or deficient for w and
  dm. Male lethal. Survives as a w female when
  heterozygous with Df(1)w[258-45] = Df(1)3B4-C2;3C1-4,
  Df(1)w[rJ1] = Df(1)3A2-3;3C1-3, and Df(1)w[rJ2] =
  Df(1)3A6-8;3C1-3.
#
Df(1)w[vco] Deficiency (1) white-variegated cobbled
 cytology: Df(1)2B17-C1;3C4-5.
 origin: Aneuploid segregant from T(1;3)w[vco]/+.
#
Df(1)w-ec: Deficiency (1) white-echinus
 cytology: Df(1)3C1-2;3E7-8.
 origin: Aneuploid segregant from T(1;2)w-Ec/+.
 synonym: Df(w-ec)[64d].
#
Df(1)y[3PL]sc[8R]
 cytology: Df(1)1A;1B2-3.
 origin: Associated with In(1)y[3PL]sc[8R].
#
Df(1)y[4L]sc[4R]
 cytology: Df(1)1A8-B1;1B3-4 + Df(1)18A3-4;19F-20C1.
 origin: Associated with In(1)y[4L]sc[4R].
#
Df(1)y[4L]sc[8R]
 cytology: Df(1)1A8-B1;1B2-3 + Df(1)18A3-4;20B-D1.
 origin: Associated with In(1)y[4L]sc[8R].
#
Df(1)y[4L]sc[9R]
 cytology: Df(1)1A8-B1;1B2-3 + Df(1)18A3-4;18B8-9.
 origin: Associated with In(1)y[4L]sc[9R].
#
Df(1)z1: Deficiency (1) zeste
 cytology: Df(1)2C2-3;3E2-3.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg. Suppl. 38: 1-90 (fig.).
 genetics: Deficient for pn, z, and w. Male lethal.
#
Df(1)z2
 cytology: Df(1)2D4-5;3C3-4.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg. Suppl. 38: 1-90 (fig.).
 genetics: Deficient for pn, z, and w. Male lethal.
#
Df(1)z3
 cytology: Df(1)2C5-6;3B2-3.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg. Suppl. 38: 1-90 (fig.).
 genetics: Deficient for pn and z. Male lethal.
#
Df(1)z4
 cytology: Df(1)2C5-6;3A9-B1.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg. Suppl. 38: 1-90
  (fig.).
 genetics: Deficient for pn and z. Male lethal.
#
Df(1)z5
 cytology: Df(1)3A1-3;3A4-6.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg. Suppl. 38: 1-90
  (fig.).
 genetics: Deficient for z. Male lethal.
#
Df(1)z6
 cytology: Df(1)3A6-8;3C10-11.
 origin: X ray induced in z.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg. Suppl. 38: 1-90 (fig.).
 genetics: Deficient for w but not z. Male lethal.
#
Df(Y)bb: Deficiency (Y) bobbed
 cytology: Metaphase chromosomes show short arm of Y reduced to
  one-third normal size.
 origin: Spontaneous.
 discoverer: Schultz, 33k8.
 genetics: Deficient for bb but not KL or KS.
#
Df(2L)64j
 cytology: Df(2L)34E5-F1;35C3-D1.
 origin: X ray induced.
 discoverer: E. H. Grell, 1964.
 genetics: Deficient for rk, b, j, el, Sco, Su(H), pu, and
  Adh but not for nub, M(2)e, rd, or M(2)m.
  Homozygous lethal.
#
Df(2L)al: Deficiency (2L) aristaless
 cytology: Df(2L)21B8-C1;21C8-D1.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 147-51.
 genetics: Deficient for al, ex, and ds but not for l(2)gl,
  net, or S. Homozygous lethal.
#
Df(2L)b[D]: Deficiency (2L) black-Dominant
 cytology: Df(2L)35C;35D (Kodani).
 origin: Spontaneous.
 discoverer: Goldschmidt, 1945.
 references: 1945, Univ. Calif. (Berkeley) Publ. Zool. 49: 504, 520.
 genetics: Possibly deficient for b. Homozygous lethal.
#
Df(2L)C263 Deficiency (2L) Crossover suppressor
 cytology: Df(2L)25F;26F.
 origin: Associated with In(2L)C263.
#
Df(2L)Cy[L]t[R]
 cytology: Df(2L)22D1-2;22D3-E1 + Df(2L)33F5-34A1;34A8-9.
 origin: Associated with In(2L)Cy[L]t[R].
#
Df(2L)d: Deficiency (2L) dachs
 origin: Spontaneous in d stock.
 discoverer: Bridges, 15j6.
 synonym: d[l]: dachs-lethal.
 references: Bridges and Morgan, 1919, Carnegie
  Inst. Wash. Publ. No. 278: 277.
 genetics: Homozygous lethal. Gives decreased crossing over in
  d-b region.
#
Df(2L)G
 cytology: Df(2L)36B5-6;40F.
 origin: Aneuploid segregant from T(Y;2)G/+.
#
Df(2L)H
 cytology: Df(2L)37B2-3;40B2-3.
 origin: Aneuploid segregant from T(Y;2)H/+.
#
Df(2L)M-z[B]: Deficiency (2L) Minute-z-B
 cytology: Df(2L)24E2-F1;25A1-2.
 origin: Spontaneous.
 discoverer: Bridge, 38d12.
 synonym: Df(2L)M-B.
 references: Morgan, Schultz, Bridges, and Curry, 1939, Carnegie
  Inst. Wash. Year Book 38: 276-77.
  Curry, 1939, DIS 12: 46.
  1941, DIS 14: 50.
 genetics: Deficient for M(2)z, dp, and dw-24F but not
  ed, ft, G, M(2)S1, 1(2)cg, or tkv.
  Homozygous lethal.
#
Df(2L)M-z[C]
 cytology: Df(2L)24D2-5;25A2-3.
 origin: Spontaneous.
 discoverer: Curry, 37g27.
 synonym: Df(2L)M-C.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 307.
  Morgan, Schultz, Bridges, and Curry, 1939, Carnegie
  Inst. Wash. Year Book 38: 276-77.
 genetics: Deficient for ed, ft, G, M(2)z, dp, and
  dw-24F but not M(2)S1, l(2)cg, or tkv.
  Homozygous lethal.
#
Df(2L)S[56f]: Deficiency (2L) Star
 cytology: Df(2L)21C6-D1;22A3-B1.
 origin: Associated with In(2LR)S[56f].
#
Df(2L)S-der: Deficiency (2L) Star derived
 cytology: Df(2L)21D4-E1;21E2-3.
 new order:: Y|21D4 - 21A;
  60 - 21E3|101.
 origin: Synthetic; a combination of 2L[D]Y[P] from
  T(Y;2)21E = T(Y;2)21D4-E1 and 4[D]2[P]
  from T(2;4)ast[v] = T(2;4)21E2-3;101.
 discoverer: E. B. Lewis.
 references: 1945, Genetics 30: 137-66.
 genetics: Deficient for S and ast. Homozygous lethal.
#
Df(2L)S1
 cytology: Df(2L)21C3-4;22A2-3.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 147-51.
 genetics: Deficient for ds, S, and ast but not
  l(2)gl, net, al, ex, shr, or ho. Homozygous
  lethal.
#
Df(2L)S2
 cytology: Df(2L)21C6-D1;22A6-B1.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 147-51.
 genetics: Deficient for ds, S, ast, and shr but not
  l(2)gl, net, al, ex, or ho. Homozygous
  lethal.
#
Df(2L)S3
 cytology: Df(2L)21D2-3;21F2-22A1.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 147-51.
 genetics: Deficient for S and ast but not l(2)gl,
  net, al, ex, ds, shr, or ho. Homozygous
  lethal.
#
Df(2L)S4
 cytology: Df(2L)21C3-4;22B2-3.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 147-51.
 genetics: Deficient for ds, S, ast, and shr but not
  l(2)gl, net, al, ex, or ho. Homozygous
  lethal.
#
Df(2L)S5
 cytology: Df(2L)21C2-3;22A3-4.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 147-51.
 genetics: Deficient for ex, ds, S, and ast but not
  l(2)gl, net, al, shr, or ho. Homozygous
  lethal.
#
Df(2L)S7
 cytology: Df(2L)21C3-4;21F2-22A1.
 origin: X ray induced in net ho.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 147-51.
 genetics: Deficient for ds, S, and ast but not
  l(2)gl, al, ex, or shr. Homozygous lethal.
#
Df(2L)Sw-L: Deficiency (2L) Swedish-L
 cytology: Tip of 2L contains deficiency.
 origin: Naturally occurring condition in some Swedish
  strains.
 discoverer: Gustafson, 1937.
 genetics: No phenotypic effect.
#
Df(2R)42
 cytology: Df(2R)42C3-8;42D2-3.
 origin: Probably X ray induced. Found on chromosome with
  vg[S].
 discoverer: Bridges, 36b.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 304-9.
 genetics: Deficient for no tested loci. Homozygous lethal.
#
Df(2R)a[ba2]: Deficiency (2R) arc-broad angular
 cytology: Df(2R)58D5-6;58D7-8.
 origin: Spontaneous.
 discoverer: Goldschmidt.
 references: 1945, Univ. Calif. (Berkeley)
  Publ. Zool. 49: 363-73, 388-89.
 genetics: Associated with s[ba2].
#
Df(2R)bw[5]: Deficiency (2R) brown
 cytology: Df(2R)59D10-E1;59E4-F1.
 origin: Spontaneous.
 discoverer: Mohr, 31k28.
 genetics: Deficient for bw. Homozygous lethal.
#
Df(2R)bw[AL]Cy[R]
 cytology: Df(2R)41;42A2-3.
 origin: Associated with In(2R)bw[AL]Cy[R].
#
Df(2R)bw[R40]: Deficiency (2R) brown-Rearranged
 cytology: Df(2R)59C5-6;50E2-3.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R40].
#
Df(2R)bw[V34kL]Cy[L]
 cytology: Df(2R)41;42A2-3.
 origin: Aneuploid recombinant from In(2R)bw[V34k]+Cy/+.
#
Df(2R)bw[VDe1L]Cy[R]
 cytology: Df(2R)41B2-C1;42A2-3.
 origin: Associated with In(2R)bw[VDe1L]Cy[R].
#
Df(2R)bw[VDe2L]Cy[R]
 cytology: Df(2R)41A-B;42A2-3.
 origin: Associated with In(2R)bw[VDe2L]Cy[R].
#
Df(2R)Cy[L]bw[VDe1R]
 cytology: Df(2R)58A4-B1;59E2-4.
 origin: Associated with In(2R)Cy[L]bw[VDe1R].
#
Df(2R)Cy[L]bw[VDe2R]
 cytology: Df(2R)58A4-B1;59D6-E1.
 origin: Associated with In(2R)Cy[L]bw[VDe2R].
#
Df(2R)Cy[R]bw[V34kR]
 cytology: Df(2R)58A4-B1;59.
 origin: Aneuploid recombinant from In(2R)bw[V34k]+Cy/+.
#
Df(2R)M-c[33a]: Deficiency (2R) Minute-c
 cytology: Df(2R)60E2-3;60E11-12.
 origin: X ray induced.
 discoverer: Schultz, 33a7.
 synonym: Df(2)M-33a.
 references: Bridges, 1937, Cytologia (Tokyo), Fujii Jub.,
  Vol. 2: 745-55.
 genetics: Deficient for M(2)c. Homozygous lethal.
#
Df(2R)M-l
 cytology: Df(2R)57F11-58A1;58F8-59A1.
 origin: Spontaneous.
 discoverer: Bridges, 23g15.
 references: Morgan, Bridges, and Sturtevant, 1925,
  Bibliog. Genet. 2: 231.
  Bridges, 1937, Cytologia (Tokyo), Fujii
  Jub., Vol. 2: 745-55.
 genetics: Deficient for px, l(2)Su(H), M(2)l, and probably
  a. Homozygous lethal.
#
Df(2R)M-S2: Deficiency (2R) Minute of Schultz 2
 cytology: Salivary chromosomes apparently normal. Located in
  chromocentric region of 41A.
 origin: X ray induced.
 discoverer: Schultz, 33a12.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 306.
  Morgan, Schultz, Bridges, and Curry, 1939, Carnegie
  Inst. Wash. Year Book 38: 273-77.
  Morgan, Schultz, and Curry, 1940, Carnegie
  Inst. Wash. Year Book 39: 251-55.
 genetics: Lethal homozygous; mutant phenotype with stw but
  not Jag, lt, rl, ap, tk, std, or msf;
  judged a deficiency on this basis.
#
Df(2R)M-S2[4]
 cytology: Salivary chromosomes apparently normal.
 origin: X ray induced.
 discoverer: Schultz, 33a5.
 synonym: Df(2R)M-S4.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 306.
  Morgan, Schultz, Bridges, and Curry, 1939, Carnegie
  Inst. Wash. Year Book 38: 273-77.
  Morgan, Schultz, and Curry, 1940, Carnegie
  Inst. Wash. Year Book 39: 251-55.
 genetics: Gives mutant phenotype with stw and ap.
  Lethal homozygous and with M(2)S2, l(2)Sp9c,
  l(2)Sp11, and l(2)Sp15. No interaction with
  Jag, lt, rl, tk, std, or msf. Judged a
  deficiency on the basis of genetic evidence.
#
Df(2R)M-S2[8]
 cytology: Salivary chromosomes appear normal.
 origin: X ray induced.
 discoverer: Schultz, 33a3.
 synonym: Df(2R)M-S8.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 306.
  Morgan, Schultz, Bridges, and Curry, 1939, Carnegie
  Inst. Wash. Year Book 38: 273-77.
 genetics: Lethal homozygous and with M(2)S2, l(2)Sp9c,
  l(2)Sp11, and l(2)Sp15. Gives mutant
  phenotype with stw but not rl or ap.
#
Df(2R)M-S2[10]
 cytology: Df(2R)41A. In mitotic metaphase, 2R about
  three-fourths normal size.
 origin: X ray induced.
 discoverer: Schultz, 32k22.
 synonym: Df(2R)M-S10.
 references: Morgan, Schultz, Bridges, and Curry, 1939, Carnegie
  Inst. Wash. Year Book 38: 273-77.
  Morgan, Schultz, and Curry, 1940, Carnegie
  Inst. Wash. Year Book 39: 251-55.
  1941, Carnegie Inst. Wash. Year
  Book 40: 282-87.
 genetics: Lethal homozygous and with M(2)S2, l(2)Sp9c,
  l(2)Sp11, and l(2)Sp15. Gives mutant phenotype
  with rl but not stw or ap.
#
Df(2R)M-S2[D]
 cytology: Df(2R)41A;41C.
 origin: Associated with T(Y;2;3)D.
#
Df(2R)M-S2[vg11] Deficiency (2R) Minute of Schultz 2 from vestigial 11
 cytology: Df(2R)40F-41A1;42A19-B1.
 origin: X ray induced; arose simultaneously with vg[11].
 discoverer: Ruch, 1931.
 synonym: Df(2R)M-vg[11].
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 306.
  Morgan, Schultz, Bridges, and Curry, 1939, Carnegie
  Inst. Wash. Year Book 38: 275.
 genetics: Deficient for rl, M(2)S2, stw, ap, tk, and
  msf but not ltd. Homozygous lethal.
#
Df(2R)Np: Deficiency (2R) Notopleural
 cytology: Df(2R)44F1-2;45E1-2 |idges).
 origin: Spontaneous.
 discoverer: Nichols-Skoog, 33b20.
 references: Bridges, Skoog, and Li, 1936, Genetics 21: 788-95
  (fig.).
  Li, 1936, Peking Nat. Hist. Bull. 11: 39-48.
 genetics: Not deficient for cn, blo, or en.
  Df(2R)Np/T(2;3)dp lethal and homozygous lethal.
#
Df(2R)Ore-R: Deficiency (2R) Oregon-R
 cytology: Df(2R)60F2-3; terminal deficiency.
 origin: Naturally occurring in Oregon-R stock.
 discoverer: Bridges, 36l5.
 genetics: No detectable phenotypic effect in homozygote.
#
Df(2R)P
 cytology: Df(2R)58E3-F1;60D14-E2.
 origin: Aneuploid segregant from T(2;3)P/+.
#
Df(2R)Px: Deficiency (2R) Plexate
 cytology: Df(2R)60B8-10;60D1-2.
 origin: Spontaneous.
 discoverer: Bridges, 22f6.
 references: 1937, Cytologia (Tokyo), Fujii Jub., Vol. 2: 745-55.
 genetics: Deficient for l(2)NS, sp, bs, ba, and Pin
  but not or, Fo, pd, ll, mr, or l(2)ax.
  Homozygous lethal.
#
Df(2R)Px[2]
 cytology: Df(2R)60C5-6;60D9-10.
 origin: X ray induced.
 discoverer: Schultz, 32l1.
 references: Bridges, 1937, Cytologia (Tokyo), Fujii Jub.,
  Vol. 2: 745-55.
 genetics: Deficient for bs, ba, and Pin but not
  l(2)NS, sp, or M(2)c. Homozygous lethal.
#
Df(2R)Px[4]
 cytology: Df(2R)60B;60D1-2.
 origin: Associated with In(2LR)Px[4].
#
Df(2R)Px[5]
 origin: Spontaneous in In(2LR)bw[V1].
 discoverer: Thompson, 1957.
 references: 1963, DIS 38: 28.
 genetics: Deficient for bs and ba but not sp.
  Homozygous lethal.
#
Df(2R)Sw: Deficiency (2R) Swedish
 cytology: Df(2R)60F3-4; terminal deficiency.
 origin: Natural condition of Swedish-b.
 discoverer: Catcheside, 36l20.
 genetics: No phenotypic effect.
#
Df(2R)vg[B]: Deficiency (2R) vestigial-Beaded
 cytology: Df(2R)49D3-4;50A2-3.
 origin: Spontaneous.
 discoverer: Bridges, 28d11.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 304-6.
 genetics: Deficient for vg and l(2)C but not sca.
  Homozygous lethal.
#
Df(2R)vg[C]: Deficiency (2R) vestigial-Carved
 cytology: Df(2R)49B2-3;49E7-F1.
 origin: X ray induced.
 discoverer: Demerec, 28c3.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 304-6.
 genetics: Deficient for sca, vg, and l(2)C. Homozygous
  lethal.
#
Df(2R)vg[D]: Deficiency (2R) vestigial-Depilate
 cytology: Df(2R)49C1-2;49E2-6.
 origin: Spontaneous.
 discoverer: Bridges, 31a22.
 references: Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 304-6.
 genetics: Deficiency for sca, vg, and l(2)C.
  Homozygous lethal.
#
Df(2R)vg[I]: Deficiency (2R) vestigial-Incised
 cytology: Df(2R)49C2-D1;50A2-3.
 discoverer: Bridges, 36d20.
 references: Morgan, Bridges, and Schultz, 1938,
  Carnegie Inst. Wash. Year Book 37: 304-6.
 genetics: Deficient for sca, vg, and l(2)C.
  Homozygous lethal.
#
Df(2R)vg[S]: Deficiency (2R) vestigial-Snipped
 cytology: Df(2R)49B12-C1;49F15-50A1.
 origin: X ray induced.
 discoverer: Muller, 1929.
 references: 1930, J. Genet. 22: 299-334.
  Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 304-6.
 genetics: Deficient for sca, vg, and l(2)C.
  Homozygous lethal.
#
Df(3L)D: Deficiency (3L) from T(Y;2;3)D
 cytology: Df(3L)61E2-F1;62A4-6.
 origin: Associated with T(Y;2;3)D.
#
Df(3L)h[100.390]: Deficiency (3L) hairy
 cytology: Df(3L)66D2-5;66D14-E1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for h. Homozygous lethal.
#
Df(3L)Hn: Deficiency (3L) Henna
 cytology: Df(3L)66A;66B.
 origin: X ray induced simultaneously with T(2;3)Hn =
  T(2;3)53E-54A;77A;94F;96A.
 discoverer: Van Atta, 30k.
 references: 1932, Am. Naturalist 66: 93-95.
  1932, Genetics 17: 637-59.
  Lewis, 1956, DIS 30: 130.
 genetics: Mutant or deficient for Hn. Homozygous lethal.
#
Df(3L)K: Deficiency (3L) of Krivshenko
 cytology: Df(3L)61C1-2; apparently a terminal
  deficiency.
 origin: Probably X ray induced.
 discoverer: Krivshenko, 56l4.
 synonym: Df-3L[K].
 references: 1959, DIS 33: 95.
#
Df(3L)Ly: Deficiency (3L) Lyra
 cytology: Df(3L)70A2-3;70A5-6.
 origin: X ray induced.
 discoverer: Dubinin, 1929.
 references: Morgan, Bridges, and Schultz, 1937, Carnegie
  Inst. Wash. Year Book 36: 301.
 genetics: Associated with the mutant, Ly. Lethal
  homozygous and in combination with
  Df(3L)M-h[33j].
#
Df(3L)M-h[33j]: Deficiency (3L) Minute-h
 cytology: Probably includes bands in 70A.
 origin: X ray induced.
 discoverer: Demerec, 33j25.
 references: 1935, DIS 3: 27.
  Coyne, 1935, DIS 4: 59.
  Mossige, 1938, Hereditas 24: 110-16.
 genetics: Deficient for M(3)h; lethal homozygous and in
  combination with Df(3L)Ly.
#
Df(3L)Mz Deficiency (3L) from Minute (2) z stock
 cytology: Loss of several bands from tip of 3L.
 origin: Spontaneous.
 discoverer: Bridges, 36h28.
#
Df(3L)N[264-6]; Deficiency (3L) Notch
 cytology: Df(3L)73E;80C.
 origin: Aneuploid segregant from T(1;3)N[264-6]/+.
#
Df(3L)ru[100.392]: Deficiency (3L) roughoid
 cytology: Df(3L)61E;62A10-B1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for ru. Homozygous lethal.
#
Df(3L)ru[100.393]
 cytology: Df(3L)61F2-3;62A4-6.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for ru. Homozygous lethal.
#
Df(3L)ru[300.234]
 cytology: Df(3L)61E;62A2-4.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for ru. Homozygous lethal.
#
Df(3L)ru-K1 Deficiency (3L) roughoid of Krivshenko
 cytology: Df(3L)62A12-B1;62B2-3.
 origin: X ray induced.
 discoverer: Krivshenko, 1957.
 references: 1958, DIS 32: 81.
 genetics: Has rough and slightly reduced eyes in combination
  with ru but, judging from cytology, probably not
  deficient for ru.
#
Df(3L)ru-K2
 cytology: Df(3L)61F4-5;62A10-B1.
 origin: X ray induced.
 discoverer: Krivshenko, 1957.
 references: 1958, DIS 32: 81.
 genetics: Deficient for ru.
#
Df(3L)st[100.62]: Deficiency (3L) scarlet
 cytology: Df(3L)73A2-3;73A10-B1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for st. Homozygous lethal.
#
Df(3L)st[100.171]
 cytology: Df(3L)72E4-5;74C2-3.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for st. Homozygous lethal.
#
Df(3L)st[100.200]
 cytology: Df(3L)72E4-5;73A10-B1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for st. Homozygous lethal.
#
Df(3L)th[100.105]: Deficiency (3L) thread
 cytology: Df(3L)72A2-B1;73A4-5.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for th and st. Homozygous lethal.
#
Df(3L)Vn: Deficiency (3L) Vein
 cytology: Df(3L)64C12-D1;65D2-E1.
 origin: Spontaneous.
 discoverer: Mohr, 28j21.
 references: 1932, Proc. Intern. Congr. Genet., 6th.,
  Vol 1: 199-212.
  1938, Norske Videnskaps-Akad. 4: 1-7.
  Mohr and Mossige, 1943, Norske
  Videnskaps-Akad. 7: 1-51 (fig.).
 genetics: Deficient for jv, dv, and Me but not for
  a-3, Hn, or se. Mutant or deficient for
  Vn. Homozygous lethal.
#
Df(3R)89EF
 cytology: Df(3R)89D7-E1;90A2-3.
 origin: Synthetic. Made by combining the 3R[D]4[P]
  element of one T(3;4) with the
  4[D]3R[P] element of another.
 discoverer: Dubovsky and Kelstein.
 references: 1936, Eksperim. Med. No. 11: 65-84.
  Kelstein, 1938, Biol. Zh. (Moscow) 7: 1145-69.
  Pipkin, 1959, Texas Univ. Publ. 5914: 69-88.
 phenotype: Heterozygote (presumably with two X's)
  resembles female intersexes and is sterile. Male
  has rotated genitalia.
 genetics: One of a series of deficiencies for the middle of 3R
  synthesized and carefully studied by Dubovsky and
  Kelstein. Heterozygous male has rotated genitalia
  which may be feminized both in structure and color,
  has sex combs. Heterozygous female sterile.
#
Df(3R)bxd[100]: Deficiency (3R) bithoraxoid
 cytology: Df(3R)89B5-6;89E2-3.
 origin: Aneuploid recombinant from Tp(3)bxd[100]/+.
#
Df(3R)bxd[110]
 cytology: Df(3R)91C7-D1;92A2-3.
 origin: Aneuploid recombinant from Tp(3)bxd[110]/+.
#
Df(3R)Dl: Deficiency (3R) Delta
 cytology: Df(3R)90D2-4;90D5-E1.
 origin: Spontaneous.
 discoverer: Schultz.
 genetics: Found in Dl but, judging from other information
  placing the locus of Dl in region 91,
  Df(3R)Dl is separable from Dl. Homozygous
  lethal.
#
Df(3R)Dl[H]
 cytology: Df(3R)91C6-D1;92A2-3 (Slizynski).
 origin: Induced by unspecified chemical.
 discoverer: Auerbach.
 references: 1943, DIS 17: 49.
 genetics: Deficient for Dl. Homozygous lethal.
#
Df(3R)e[4.39]: Deficiency (3R) ebony
 cytology: Df(3R)93B;93F.
 origin: X ray induced.
 discoverer: Alexander.
 references: 1960, Genetics 45: 1019-22.
 genetics: Deficient for e. Homozygous lethal.
#
Df(3R)e[100.172]
 cytology: Df(3R)93B7-10;93F10-94A1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for e. Homozygous lethal.
#
Df(3R)e[100.256]
 cytology: Df(3R)93A5-B1;93F5-9.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for e. Homozygous lethal.
#
Df(3R)M-S31: Deficiency (3R) Minute of Schultz
 origin: X ray induced.
 discoverer: Schultz, 33a10.
 references: 1940, DIS 13: 51.
 genetics: Termed deficiency on the basis of Minute phenotype
  and mutant interaction with cu but not ma.
  Homozygous lethal.
#
Df(3R)Na: Deficiency (3R) from Naples
 cytology: Df(3R)96F11-97A1;97A2-5.
 origin: Associated with In(3R)Na.
#
Df(3R)P14: Deficiency (3R) from Pasadena
 cytology: Df(3R)90C2-D1;91A2-3.
 origin: X ray induced.
 discoverer: E. B. Lewis.
 genetics: Deficient for sr and gl but not k or
  Dl. Homozygous lethal.
#
Df(3R)ry: Deficiency (3R) rosy
 cytology: Df(3R)87D-E;87E-F.
 origin: X ray induced.
 discoverer: E. H. Grell, 1960.
 references: 1962, Z. Induktive Abstammungs- Vererbungslehre 93: 371-77.
 genetics: Deficient for kar and ry. Homozygous lethal.
#
Df(3R)ry[27]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for l(3)S3, mes, ry, pic, l(3)S4,
  l(3)S5, l(3)S6, l(3)26, and l(3)S7 but not
  l(3)S1, l(3)S2, or kar. Homozygous lethal.
#
Df(3R)ry[28]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for ry and l(3)26. Homozygous
  lethal.
#
Df(3R)ry[29]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for kar, mes, ry, pic, l(3)S4, l(3)S5,
  and l(3)S6 but not for l(3)S2, l(3)26, or
  l(3)S7. Homozygous lethal.
#
Df(3R)ry[30]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for ry and l(3)26 and probably for
  mes and pic. Homozygous lethal.
#
Df(3R)ry[31]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for ry and probably mes and pic
  but not for l(3)26. Homozygous lethal.
#
Df(3R)ry[32]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for ry and l(3)26 and probably for
  mes and pic. Homozygous lethal.
#
Df(3R)ry[33]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for kar, mes, ry, pic, l(3)S4, l(3)S5,
  and l(3)S6 but not for l(3)S2, l(3)26, or
  l(3)S7. Homozygous lethal.
#
Df(3R)ry[34]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for ry and probably mes and pic
  but not for l(3)26. Homozygous lethal.
#
Df(3R)ry[36]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for kar, mes, and ry but not for
  l(3)S2, pic, l(3)S4, l(3)S5, l(3)S6, l(3)26, or
  l(3)S7. Homozygous lethal.
#
Df(3R)ry[51]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for l(3)S2, kar, mes, ry, pic, l(2)S4,
  l(3)S5, l(3)S6, and l(3)26 but not for l(3)S7.
  Homozygous lethal.
#
Df(3R)ry[52]
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for l(3)S3, mes, ry, pic, l(3)S4,
  l(3)S5, and l(3)S6 but not for l(3)S2, kar,
  l(3)26, or l(3)S7. Homozygous lethal.
#
Df(3R)ry[66]
 origin: X ray induced.
 discoverer: Kernaghan.
 references: Schalet, 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for mes, ry, pic, l(3)S4, l(3)S5,
  l(3)S6, and l(3)26 but not for l(3)S2, kar, or
  l(3)S7. Homozygous lethal.
#
Df(3R)ry[70]
 origin: X ray induced.
 discoverer: Kernaghan.
 references: Schalet, 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for mes, ry, pic, l(3)S4, l(3)S5, and
  l(3)S6 but not for l(3)S2, kar, l(3)26, or
  l(3)S7. Homozygous lethal.
#
Df(3R)ry[74]
 origin: X ray induced.
 discoverer: Schalet.
 genetics: Deficient for the right portion of the mes region
  and for ry but not for l(3)S3, the left
  portion of the mes region, or pic.
  Homozygous lethal.
#
Df(3R)ry[75]
 origin: X ray induced in kar[2] chromosome.
 discoverer: Schalet.
 genetics: Deficient for l(3)S3, mes, ry, pic,
  l(3)S4, and l(3)S5 but not for kar or l(3)S6.
  Homozygous lethal.
#
Df(3R)ry[76]
 origin: X ray induced in kar[2] chromosome.
 discoverer: Schalet.
 genetics: Deficient for l(3)S2, kar, l(3)S3, mes, ry, pic,
  l(3)S4, and l(3)S5 but not for l(3)S1,
  l(3)S6, or l(3)26. Homozygous lethal.
#
Df(3R)ry[77]
 origin: X ray induced in kar[2] chromosome.
 discoverer: Schalet.
 genetics: Deficient for l(3)S3, mes, ry, and pic but not
  l(3)S1, l(3)S2, kar, or l(3)26. Homozygous
  lethal.
#
Df(3R)ry[78]
 origin: X ray induced in kar[2] chromosome.
 discoverer: Schalet.
 genetics: Deficient for mes, ry, pic, and l(3)26 but
  not for kar or l(3)S3. Homozygous lethal.
#
Df(3R)ry[K]: Deficiency (3R) rosy of Kernaghan
 origin: X ray induced in cu kar chromosome.
 discoverer: Kernaghan.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient for l(3)S1, l(3)S2, kar, l(3)S3, mes,
  ry, pic, l(3)S4, l(3)S5, l(3)S6, and l(3)26 but
  not l(3)S7. Homozygous lethal.
#
Df(3R)sbd[105]: Deficiency (3R) stubbloid
 cytology: Df(3R)88F9-89A1;89B4-5.
 origin: X ray induced.
 discoverer: E. B. Lewis.
 references: 1948, DIS 22: 72-73.
 genetics: Deficient for c(3)G, sbd, and Sb but not
  kar, cv-c, ss, or bx. Df(3R)sbd[105]/+
  shows decreased crossing over in X (Hinton,
  1966, Genetics 55: 157-64). Homozygous lethal.
#
Df(3R)sr[100.394]: Deficiency (3R) stripe
 cytology: Df(3R)90C2-7;90F3-7.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for sr. Homozygous lethal.
#
Df(3R)sr[300.24]
 cytology: Df(3R)90C2-4;91A2-5.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for sr. Homozygous lethal.
#
Df(3R)sr[300.101]
 cytology: Df(3R)90D2-4;91A6-8.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Deficient for sr. Homozygous lethal.
#
Df(4)3
 cytology: Df(4)102E;102F; inferred from genetic data.
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 genetics: Lethal in homozygote and in combination with
  Df(4)G, Df(4)11, Df(4)34, and spa[Cat] but
  not l(4)9 or l(4)29 (Hochman).
#
Df(4)11
 cytology: Df(4)102E2-10;102F2-10 (Hochman); salivary
  chromosome bands missing in sections 102E and
  perhaps some from 102F, but distal tip of 4R is
  present.
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 synonym: l(4)11.
 references: Hochman, Gloor, and Green, 1964, Genetica
  35: 109-26.
 genetics: Permits pseudodominant expression of sv and
  spa alleles. Heterozygote with spa shows
  slight sparkling effect, but the effect is extreme in
  heterozygote with spa[pol]. Lethal
  homozygous and with spa[Cat], l(4)9, l(4)29,
  Df(4)3, Df(4)12, Df(4)24, Df(4)34, and Df(4)G.
#
Df(4)12
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 synonym: l(4)12.
 references: Hochman, Gloor, and Green, 1964, Genetica
  35: 109-26.
 genetics: Heterozygote with spa is wild type and with
  spa[pol] is slight sparkling. Lethal
  homozygous and with spa[Cat], l(4)9, l(4)29,
  Df(4)3, Df(4)11, Df(4)24, Df(4)34, and Df(4)G.
#
Df(4)17
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 synonym: l(4)17.
 references: Hochman, Gloor, and Green, 1964, Genetica
  35: 109-26.
 genetics: Lethal homozygous and when heterozygous with
  ci[D] or Ce[2]. Does not interact with
  any other factor in Df(4)M.
#
Df(4)24
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 synonym: l(4)24.
 references: Hochman, Gloor, and Green, 1964, Genetica
  35: 109-26.
 genetics: Heterozygote with spa is sparkling and with
  spa[pol] is poliert. Lethal homozygous and
  with spa[Cat], l(4)9, l(4)29, Df(4)3, Df(4)11,
  Df(4)12, Df(4)34, and Df(4)G.
#
Df(4)31
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 synonym: l(4)31.
 references: Hochman, Gloor, and Green, 1964, Genetica
  35: 109-26.
 genetics: Lethal homozygous and when heterozygous with
  ci[D] or Ce[2]. Does not interact with
  any other factor in Df(4)M.
#
Df(4)34
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 synonym: l(4)34.
 references: Hochman, Gloor, and Green, 1964, Genetica
  35: 109-26.
 genetics: Lethal homozygous and when heterozygous with
  Df(4)G, Df(4)11, Df(4)3, and spa[Cat] but
  not with l(4)9 or l(4)29.
#
DF(4)G: Deficiency (4) of Gloor and Green
 cytology: Df(4)102E2-10; tip of 4R lost and remainder of
  chromosome 4 capped with X-chromosomal
  material, including 1A (Hochman).
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 references: Hochman, Gloor, and Green, 1964, Genetica
  35: 109-26.
 genetics: Lethal homozygous and in heterozygous combination
  with Df(4)3, Df(4)11, Df(4)12, Df(4)24, Df(4)34,
  spa[Cat], l(4)9, and l(4)29. Recessives at
  sv and spa loci expressed fully in
  heterozygote. Loci of y[+] and ac[+]
  linked to the chromosome.
#
Df(4)M: Deficiency (4) Minute
 cytology: Df(4)101E-F;102B6-17; right break to the left
  of 102B9-10 according to Bridges, to the right
  according to Slyzinski (1944, J. Heredity
  35: 322-24). Hochman has not succeeded in
  distinguishing between these alternatives.
 origin: Spontaneous.
 discoverer: Bridges, 25l28.
 synonym: Df(4)M-4.
 references: 1935, Biol. Zh. (Moscow) 4: 401-20.
  1935, Tr. Dinam. Razvit. 10: 469.
 genetics: Deficient for ar, ci, gvl, l(4)1, l(4)13, l(4)18,
  l(4)25, M(4), and Scn but not bt, l(4)2,
  sv, or spa. Homozygous lethal.
#
Df(4)M[2]
 origin: X ray induced.
 discoverer: Schultz, 32k29.
 references: Bridges, 1935, Biol. Zh. (Moscow) 4: 401-20.
 genetics: Deficient for ar, ci, and ci[D].
  Homozygous lethal.
#
Df(4)M[3]
 cytology: Df(4)101E;102B; similar to Df(4)M
  |idges, 1935, Tr. Dinam. Razvit 10: 470).
 origin: X ray induced.
 discoverer: Schultz, 33a8.
 synonym: Df(4)M-4[3].
 genetics: Deficient for ar, ci, gvl, and M(4) but not
  bt, ey, or sv. Homozygous lethal.
#
Df(4)M[4]
 origin: X ray induced.
 discoverer: Glass, 42h12.
 references: 1944, DIS 18: 40.
 genetics: Deficient for Ce, ci, and M(4) but not for
  ey or sv. Homozygous lethal.
#
Df(4)M[62e]
 cytology: Df(4)101E;102D13-E1.
 origin: Recovered among progeny of male injected with
  Drosophila DNA.
 discoverer: Fahmy, 62e.
 genetics: Deficient for ar, ci, gvl, and ey; Fahmy
  claimed it was also deficient for spa but not
  sv. If we assume that Df(4)M[62e] is a
  simple interstitial deficiency, Fahmy's claim
  contradicts all other evidence on the order of
  sv and spa. Hochman finds that
  Df(4)M[62e]/spa[pol] is poliert. Homozygous
  lethal.
#
Df(4)M[62f]
 cytology: Df(4)101E;102B10-17 (Fahmy);
  Df(4)101E-F;102B2-5 (Hochman).
 origin: Gamma ray induced.
 discoverer: Fahmy, 62f.
 genetics: Deficient for ar, ci, gvl, and M(4) but not
  bt, ey, sv, or spa. Homozygous lethal.
#
Df(4)M[63a]
 cytology: Df(4)101F2-102A1;102A2-5 (combined from
  observations of Fahmy and Hochman).
 origin: Recovered from progeny of male injected with thymus
  extract from leukemic mice (Gross Factor).
 discoverer: Fahmy, 63a.
 genetics: Deficient for ci and M(4) but not ar, gvl,
  bt, ey, sv, spa, or the lethal effect of
  ci[D]. Homozygous lethal.
#
Dp(1;1)100: Duplication (1;1) 100
 origin: Spontaneous product of exchange between
  Dp(1;f)100 and proximal heterochromatin of
  C(1)RM.
#
Dp(1;1)105
 cytology: Metaphase X chromosome has one arm of normal
  length and one about 40% normal length.
 new order:: 1 - 20|6 - 1.
 origin: X-ray-induced deletion of most of X euchromatin
  was recovered as a C(1)RM/Dp(1;f)105 female,
  which by detachment produced Dp(1;1)105 in the
  succeeding generation.
 discoverer: Dobzhansky, 1930.
 references: 1932, Biol. Zentr. 52: 493-509.
 genetics: Contains wild-type alleles of y through dx
  and also probably bb.
#
Dp(1;1)112
 origin: Spontaneous product of exchange between
  Dp(1;f)112 and proximal heterochromatin of an
  attached X.
#
Dp(1;1)138
 origin: X-ray-induced deletion of most of X euchromatin
  that was recovered as a C(1)RM/Dp(1;f)138
  female, which by detachment produced Dp(1;1)138
  in the subsequent generations.
 discoverer: Dobzhansky, 1930.
 references: 1935, Z. Induktive Abstammungs- Vererbungslehre
  68: 134-62.
 genetics: Extends from locus of r to base of X;
  carries B. Female nearly wild type, but male
  has low viability and is sterile.
#
Dp(1;1)258-46
 cytology: Dp(1;1)2B4-7;3A4-6; reversed repeat
  (Sutton).
 new order:: 1 - 2B4|3A4 - 2B7|2B7 - 20 or
  1 - 3A4|3A4 - 2B7|3A6 - 20.
 origin: X ray induced.
 discoverer: Demerec, 38l.
 genetics: Originally appeared as w but reverted to
  w[+]. M(1)Bld, tw, br, pn, kz, and gt not
  affected.
#
Dp(1;1)B: Duplication (1;1) Bar
 cytology: Dp(1;1)15F9-16A1;16A7-B1; a tandem duplication
  |idges, 1936, Science 83: 210-11; Muller,
  Prokofyeva-Belgovskaya, and Kossikov, 1936,
  Dokl. Acad. Nauk SSSR 1: 87-88).
 new order:: 1 - 16A7|16A1 - 20.
 origin: Spontaneous.
 discoverer: Tice, 13b.
 references: 1914, Biol. Bull. 26: 221-30.
 genetics: Position effect for B, apparently resulting
  from juxtaposition of 16A1 with 16A7, which may
  undergo mutation to less extreme forms
  (e.g., B[i]).
  Produces normal and triplicated [Dp(1;1)BB]
  products by unequal crossing over.
#
Dp(1;1)B[263-28]
 cytology: Dp(1;1)15F9-16A1;16A3-4;16A6-7;16A7-B1.
 new order:: 1 - 16A3|16A7|16A1 - 20.
 origin: X-ray-induced deletional derivative of
  Dp(1;1)B[i]B[i] = Dp(1;1)15F9-16A1;16A7-B1.
 discoverer: Demerec, 34b.
 references: Sutton, 1943, Genetics 28: 97-107.
#
Dp(1;1)B[263-48]
 cytology: Dp(1;1)3E2-3;15F9-16A1;20A2-3.
 origin: Recombinant product from Tp(1)B[263-48]/+.
#
Dp(1;1)B[S]RAG Duplication (1;1) Bar of Stone Reversed Acrocentrigenic
 cytology: Dp(1;1)15F9-16A1;20.
 new order:: .20|1A - 20|20 - 16A1|102F.
 origin: Spontaneous recombinant between the distal X of
  a C(1)RA and 4[D]X[P] from
  T(1;4)B[S].
 discoverer: Lindsley and Sandler.
 references: 1963. In Methology in Basic Genetics,
  W. J. Burdette, ed., Holden-Day,Inc., pp. 390-403.
 genetics: Generates reversed acrocentric compound X
  chromosomes in Dp(1;1)B[S]RAG/+ female,
  usually by a double exchange in which one exchange
  occurs between the duplicated segment of one strand
  and the homologous region of its sister and the
  other between the duplication-bearing X and its
  normal homolog. Rate of C(1)RA generation about
  6 x 10[-4].
#
Dp(1;1)B[S]RMG Duplication (1;1) Bar of Stone Reversed Metacentrigenic
 cytology: Dp(1;1)15F9-16A1;20.
 new order:: 1 - 20.20 - 16A1|102F.
 origin: Spontaneous recombinant between C(1)RM and the
  4[D]X[P] element of T(1;4)B[S].
 discoverer: Muller.
 synonym: Doubler.
 references: 1936, DIS 6: 8.
  Lindsley and Sandler, 1963. In Methodology in Basic
  Genetics, W. J. Burdette, ed., Holden-Day, Inc.,
  pp. 390-403.
 genetics: Generates reversed metacentric compound X
  chromosomes in Dp(1;1)B[S]RMG/+ female by
  crossing over between the duplicated segment and
  either the X to which it is attached or the
  homologous X at a rate of about
  2.5 x 10[-4].
#
Dp(1;1)B[S]TAG Duplication (1;1) Bar of Stone Tandem Acrocentrigenic
 cytology: Dp(1;1)15F9-16A1;20.
 new order:: .20 - 1A|20 - 16A1|102F.
 origin: X-ray-induced recombinant between the distal
  heterochromatin of an X chromosome with a
  terminal heterochromatic segment derived from
  y[+]Y and the proximal heterochromatin of the
  4[D]X[P] element of T(1;4)B[S].
 discoverer: Lindsley and Sandler.
 references: 1963. In Methodology in Basic Genetics,
  W. J. Burdette, ed., Holden-Day, Inc., pp. 390-403.
 genetics: Ineffective in generating tandem acrocentric
  compound X chromosomes.
#
Dp(1;1)B[S]TMG Duplication (1;1) Bar of Stone Tandem Metacentrigenic
 cytology: Dp(1;1)15F9-16A1;20 added as a second arm to
  In(1)sc[8L]EN[R].
 new order:: 1A - B2|20B - 1A|20.20 - 16A1|102F.
 origin: Spontaneous recombinant between the X in
  normal sequence of a C(1)TM and the
  4[D]X[P] element of T(1;4)B[S].
 discoverer: Lindsley and Sandler.
 references: 1963. In Methodology in Basic Genetics,
  W. J. Burdette, ed., Holden-Day, Inc., pp. 390-403.
 genetics: Generates tandem metacentric compound X
  chromosomes in Dp(1;1)B[S]TMG/+ female by
  recombination between the duplication and the base of
  a homolog in normal sequence, at a rate of about
  20 x 10[-4].
#
Dp(1;1)B[S]TRG Duplication (1;1) Bar of Stone Tandem Ring-genic
  See C(1)TMB[S], subsection on compound
  chromosomes.
#
Dp(1;1)bb[DfL]Cl[R]
 cytology: Dp(1;1)4A5-B1;4D2-3 + Dp(1;1)17A6-B1;20B-C.
 origin: Associated with In(1)bb[DfL]Cl[R].
#
Dp(1;1)bb[DfL]y[4R]
 cytology: Dp(1;1)1A8-B1;4D2-3 + Dp(1;1)18A3-4;20B-C.
 origin: Associated with In(1)bb[DfL]y[4R].
#
Dp(1;1)BB: Duplication (1;1) Bar Bar
 cytology: Dp(1;1)15F9-16A1;16A7-B1; a tandem
  triplication [Bridges, 1936, Science 83: 210-11
  (fig.)].
 new order:: 1 - 16A7|16A1 - 16A7|16A1 - 20.
 origin: Spontaneous through unequal crossing over in B/B
  female.
 discoverer: Zeleny.
 references: 1920, J. Exptl. Zool. 30: 292-324.
  Sturtevant, 1925, Genetics 10: 117-47.
 genetics: Either or both B regions may carry a less
  extreme derivative of B (i.e., B[i]B,
  BB[i], or B[i]B[i]).
  Number of duplicated segments
  may be either increased or decreased by unequal
  crossing over.
#
Dp(1;1)Bt: Duplication (1;1) Branchlet
 cytology: Dp(1;1)3B2-C1;6F6-7; tandem repeat (Darby).
 new order:: 1 - 6F4|3C1 - 20.
 origin: Induced by P[32].
 discoverer: Bateman, 1950.
 references: 1950, DIS 24: 54.
  1951, DIS 25: 77.
#
Dp(1;1)Bx[r]: Duplication (1;1) Beadex-recessive
 cytology: Dp(1;1)17A;17E-F (E. B. Lewis).
 origin: Spontaneous.
 discoverer: Ives, 35k.
 references: 1937, DIS 7: 6.
  Green, 1952, Proc. Natl. Acad. Sci. U.S. 38: 949-53.
  1953, Genetics 38: 91-105.
  1953, Z. Induktive Abstammungs- Vererbungslehre
  85: 435-49.
 genetics: Duplicated for os[+], Bx[+], and
  fu[+]. Does not yield unequal crossovers as
  does Bx[r49k].
#
Dp(1;1)Bx[r49k]
 cytology: Dp(1;1)17A;17C (E. B. Lewis).
 origin: Spontaneous.
 discoverer: Mossige, 49k22.
 references: 1950, DIS 24: 61.
  Green, 1953, Z. Induktive Abstammungs-
  Vererbungslehre 85: 435-49.
 genetics: Duplicated for Bx[+] but not for os[+]
  or fu[+]. Unequal crossing over yields wild
  types and triplications. Quadruplications have also
  been produced.
#
Dp(1;1)Cl[L]y[4R]
 cytology: Dp(1;1)1A8-B1;4A5-B1.
 origin: Associated with In(1)Cl[L]y[4R].
#
Dp(1;1)Co: Duplication (1;1) Confluens
 cytology: Dp(1;1)3C4-5;3D6-E1; tandem duplication
  (Schultz, 1941, DIS 14: 54-55).
 new order:: 1 - 3D6|3C5 - 20.
 origin: Recovered among progeny of cold-treated fly.
 discoverer: Gottschewski, 34c.
 references: 1937, Z. Induktive Abstammungs- Vererbungslehre
  73: 131-42.
  1935, DIS 4: 7, 14, 16.
  1937, DIS 8: 12.
 genetics: The Co phenotype arises from a duplication of
  the Notch locus (salivary band 3C7).
#
Dp(1;1)Hw: Duplication (1;1) Hairy wing
 cytology: Dp(1;1)1A8-B1;1B2-3; tandem repeat (Demerec
  and Hoover, 1939, Genetics 24: 68).
 new order:: 1A1 - 1B2|1B1 - 20.
 origin: Spontaneous.
 discoverer: Bridges, 23c12.
 genetics: Duplication produces Hw phenotype.
#
Dp(1;1)NBB-8
 cytology: Dp(1;1)16A;17E; tandem duplication.
 new order:: 1 - 17E|16A - 20.
 origin: Spontaneous as nonrecombinant strand from f B os/+
  B + mother.
 discoverer: Peterson and Laughnan.
 references: 1963, Proc. Natl. Acad. Sci. U.S. 50: 126-33.
 genetics: Male viability reduced. Has a BB phenotype.
#
Dp(1;1)sc[4L]sc[8R]
 cytology: Dp(1;1)1B2-3;1B3-4.
 origin: Associated with In(1)sc[4L]sc[8R].
#
Dp(1;1)sc[4L]y[4R]
 cytology: Dp(1;1)1A8-B1;1B3-4 + Dp(1;1)18A3-4;19F-20C1.
 origin: Associated with In(1)sc[4L]y[4R].
#
Dp(1;1)sc[8L]sc[4R]
 cytology: Dp(1;1)19F-20C1;20B-D1.
 origin: Associated with In(1)sc[8L]sc[4R].
#
Dp(1;1)sc[8L]sc[L8R]
 cytology: Dp(1;1)20B-C;20B-D1.
 origin: Associated with In(1)sc[8L]sc[L8R].
#
Dp(1;1)sc[8L]y[4R]
 cytology: Dp(1;1)1A8-B1;1B2-3 + Dp(1;1)18A3-4;20B-D1.
 origin: Associated with In(1)sc[8L]y[4R].
#
Dp(1;1)sc[260-25]
 origin: Aneuploid recombinant from In(1LR)sc[260-25].
#
Dp(1;1)sc[L8L]sc[4R]
 cytology: Dp(1;1)19F-20C1;20B-C.
 origin: Associated with In(1)sc[L8L]sc[4R].
#
Dp(1;1)sc[L8L]sc[8R]
 cytology: Dp(1;1)1B2-3;1B3-4.
 origin: Associated with In(1)sc[L8L]sc[8R].
#
Dp(1;1)sc[S1L]sc[4R]
 cytology: Dp(1;1)19F-20C1;20B-D1.
 origin: Associated with In(1)sc[S1L]sc[4R].
#
Dp(1;1)sc[S1L]sc[8R]
 cytology: Dp(1;1)1B2-3;1B3-4.
 origin: Associated with In(1)sc[S1L]sc[8R].
#
Dp(1;1)sc[S1L]sc[L8R]
 cytology: Dp(1;1)20B-C;20B-D1.
 origin: Associated with In(1)sc[S1L]sc[8R].
#
Dp(1;1)sc[V1]: Duplication (1;1) scute of Valencia
 cytology: Dp(1;1)1A8-C3.
 origin: Aneuploid recombinant from In(1LR)sc[V1]/+.
#
Dp(1;1)Th: Duplication (1;1) Theta
 origin: X-ray-induced detachment of C(1)RM with
  X-ray-induced deletion of most of the X
  euchromatin.
 discoverer: Muller.
 references: Muller and Painter, 1929, Am. Naturalist 63: 197.
  Patterson, 1930, Genetics 15: 141-49.
  Muller, 1932, Proc. Intern. Congr. Genet., 6th.,
  Vol. 1: 213-55.
 genetics: Fragment of X chromosome, including y[+],
  sc[+], and bb[+] attached to right of X
  centromere. Causes development of interalar bristle
  not ordinarily present in D. melanogaster
  (Stern, 1956, Arch. Entwicklungsmech. Organ. 149: 1-25).
#
Dp(1;1)w: Duplication (1;1) white
 cytology: Dp(1;1)3A;3C.
 new order:: 1 - 3C|3A - 20.
 origin: Spontaneous as a recombinant from w[ch]/w[sp].
 discoverer: E. B. Lewis, 55j.
 references: 1957, DIS 31: 84.
 genetics: Loci of w and rst within duplicated section.
  Unequal crossing over gives normal and triplicated
  products. Quintuplication also produced.
#
Dp(1;1)w[a]: Duplication (1;1) white-apricot
 cytology: Dp(1;1)3A10-B1;3C3-5 (Gersh, 1962, Genetics 47: 1393-98).
 new order:: 1 - 3C3|3B1 - 20.
 origin: Spontaneous from w[a]/w[a] female; recovered
  once as a recombinant and once as a presumed
  recombinant.
 discoverer: Green.
 references: 1959, Genetics 44: 1243-56.
#
Dp(1;1)w[rG] Duplication (1;1) white-recombinant of Green
 cytology: Dp(1;1)3A3-4;3C1-2.
 new order:: 1 - 3C1|3A4 - 20.
 origin: A regular product of asymmetric exchange between
  3C1-2 of a w[a] or w[a2] chromosome and
  3A3-4 of specific homologs. Reciprocal of Df(1)w[rG].
 discoverer: Green, 60h21.
 synonym: Dp(1;1)3C1; Dp(1;1)w[60h21].
 references: 1961, Genetics 46: 1555-60.
  Gersh, 1962, Genetics 47: 1393-98 (fig.).
#
Dp(1;1)w[rG2]
 cytology: Dp(1;1)3B2-C1;3C3-5 [Gersh, 1962, Genetics 47: 1393-98 (fig.)].
 new order:: 1 - 3C3|3C1 - 20.
 origin: Spontaneous by recombination.
 discoverer: Green, 60h30.
 synonym: Dp(1;1)w[60h30].
#
Dp(1;1)w[rJ2] Duplication (1;1) white-recombinant of Judd
 cytology: Dp(1;1)3A6-8;3C1-3 [could be same as Dp(1;1)w[rG]].
 new order:: 1 - 3C1|3A8 - 20.
 origin: A regular product of unequal exchange between the
  3C1-3 region of a chromosome carrying w[rdp]
  with the 3A4-8 region of specific homologs. Probably
  reciprocal recombinant of Df(1)w[rJ2].
 discoverer: Judd, 1961.
 synonym: w[r,dup].
 references: 1961, Proc. Natl. Acad. Sci. U.S. 47: 545-50.
#
Dp(1;1)y[3PL]sc[8R]
 cytology: Dp(1;1)1A;1B2-3.
 origin: Associated with In(1)y[3PL]sc[8R].
#
Dp(1;1)y[bl]: Duplication (1;1) yellow-bristle
 cytology: Dp(1;1)1B2-3;4F8-9;5D4-5 (Nicoletti, Lindsley).
 new order:: 1A - 1B2|5D4 - 4F9|1B3 - 20.
 origin: Spontaneous.
 discoverer: Sandler.
 references: Sandler, Hart, and Nicoletti, 1960, DIS 34: 103-4.
 genetics: Mutant for y; duplicated for cv. Regularly
  generates further rearrangements; has produced
  losses of the duplicated segment, which are
  accompanied by changes in phenotype from y[bl]
  to y-like and a translocation between the tips
  of X and 2L accompanied by a change from
  y[bl] to y[+].
#
Dp(1;1)z1: Duplication (1;1) zeste
 cytology: Dp(1;1)1E2-3;4B4-5; tandem repeat.
 new order:: 1A - 4B4|1E3 - 20.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg., Suppl. 38: 1-90.
 genetics: Male lethal.
#
Dp(1;1)z2
 cytology: Dp(1;1)2C10-D1;4D2-4.
 origin: Associated with In(1)z2.
#
Dp(1;1)z4
 cytology: Dp(1;1)2B16-C1;3B-C1.
 new order:: 1 - 3B|3C1 - 2C1|3C1 - 20.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg., Suppl. 38: 1-90.
 genetics: Duplication male viable and fertile. Homozygous
  female viable but poorly fertile.
#
Dp(1;1)z8
 cytology: Dp(1;1)2B18-C1;4B4-5.
 new order:: 1 - 4B4|2C1 - 20.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg., Suppl. 38: 1-90.
 genetics: Lethal in male.
#
Dp(1;1)z59d
 cytology: Dp(1;1)2F5-3A1;3A4-5 (Gersh).
 new order:: 1 - 3A4|3A1 - 20.
 origin: X ray induced in y[2] su(w[a]) z.
 discoverer: Green, 59d15.
 references: 1961, Genetics 46: 1555-60.
  Gersh, 1962, Genetics 47: 1393-98 (fig.)
#
Dp(1;2)51b
 cytology: Dp(1;2)3C1-2;3D6-7;52F.
 origin: Aneuploid segregant from T(1;2)51b/+.
#
Dp(1;2)A12: Duplication (1;2) from Austin
 cytology: Dp(1;2)7A;7B.
 origin: Aneuploid segregant from T(1;2;4)A12/+.
#
Dp(1;2)A124
 cytology: Dp(1;2)10A;13A1-2;59.
 origin: Segregant from T(1;2)A124/+.
#
Dp(1;2)ct[7c1]: Duplication (1;2) cut
 cytology: Dp(1;2)7B2-3;8E2-3;25C.
 origin: Aneuploid segregant from T(1;2)ct[7c1]/+.
#
Dp(1;2)K1: Duplication (1;2) of Krivshenko
 cytology: Dp(1;2)1A5-B3;20;29A.
 origin: Associated with T(1;2)K1.
#
Dp(1;2)sc[19]: Duplication (1;2) scute
 cytology: Dp(1;2)1B1-2;1B4-7;25-26.
 origin: Aneuploid segregant from T(1;2)sc[19]/+.
#
Dp(1;2)w[m52b12]: Duplication (1;2) white-mottled
 cytology: Dp(1;2)1E5-F1;3C3-4;40-41.
 origin: Aneuploid segregant from T(1;2)w[52b12]/+.
#
Dp(1;2)w[m53a]
 cytology: Dp(1;2)3B2-C1;3C9-D1;40-41.
 origin: Aneuploid segregant from T(1;2)w[m53a]/+.
#
Dp(1;2)w[m258-44]
 cytology: Dp(1;2)3C3-4;4D2-E1;56E1-F1.
 origin: Aneuploid segregant from T(1;2;3)w[m258-44]/+.
#
Dp(1;3)126
 origin: X ray induced.
 discoverer: Dobzhansky, 1930.
 references: 1935, Z. Induktive Abstammungs- Vererbungslehre
  68: 143.
 genetics: Duplicated for r, M(1)o, f, and B but not
  sl or os; variegates for f and
  M(1)o (Schultz). Duplicated section inserted
  into chromosome 3 between st and cu.
  Also an inversion in 3L. Viability, fertility,
  and phenotype of Dp(1;3)126/+ male and female
  normal.
#
Dp(1;3)ct[11a]: Duplication (1;3) cut
 cytology: Dp(1;3)1B;7B2-3;84B.
 origin: Aneuploid segregant from T(1;3)ct[11a/+.
#
Dp(1;3)ct[12c1]
 cytology: Dp(1;3)7B2-3;7D2-6;85.
 origin: Aneuploid segregant from T(1;3)ct[12c1]/+.
#
Dp(1;3)ct[268-37]
 cytology: Dp(1;3)5D2-3;7B2-3;80C-F.
 origin: Aneuploid segregant from T(1;3)ct[268-37].
#
Dp(1;3)K2: Duplication (1;3) of Krivshenko
 cytology: Dp(1;3)20A-B;20D-F;80-81.
 origin: Associated with T(1;3)K2.
#
Dp(1;3)N[50k11]: Duplication (1;3) Notch
 cytology: Dp(1;3)1E3-4;3C6-7;89A.
 origin: Aneuploid segregant from T(1;3)N[50k11]/+.
#
Dp(1;3)N[264-58]
 cytology: Dp(1;3)3B2-3;3D6-7;80D-F.
 origin: Aneuploid segregant from T(1;3)N[264-58]/+.
 synonym: Dp(1;3)w[m264-58].
#
Dp(1;3)N[264-100]
 cytology: Dp(1;3)3B4-C1;4B4-5;80.
 origin: Aneuploid segregant from T(1;3)N[264-100]/+.
#
Dp(1;3)O4: Duplication (1;3) of Oliver
 origin: Aneuploid segregant from T(1;3)O4/+.
#
Dp(1;3)ras[v] Duplication (1;3) raspberry-variegated
 cytology: Dp(1;3)9E;13C;81F.
 origin: Aneuploid segregant from T(1;3)ras[v]/+.
#
Dp(1;3)sc[260-20]: Duplication (1;3) scute
 cytology: Dp(1;3)1A8-B1;61A1-2.
 origin: Aneuploid segregant from T(1;3)sc[260-20]/+.
#
Dp(1;3)sc[J4] Duplication (1;3) scute of Jacobs-Muller
 cytology: Dp(1;3)1B;61A.
 origin: Aneuploid segregant from T(1;3)sc[J4]/+.
#
Dp(1;3)sn[13a1]: Duplication (1;3) singed
 cytology: Dp(1;3)6C;7C9-D1;72D2-E1.
 origin: Aneuploid segregant from T(1;3)sn[13a1]/+.
#
Dp(1;3)sta: Duplication (1;3) stubarista
 cytology: Dp(1;3)1D3-E1;2A;89B21-C4.
 origin: Aneuploid segregant from T(1;3)sta/+.
#
Dp(1;3)w[m49a]: Duplication (1;3) white-mottled
 cytology: Dp(1;3)3A10-B1;3E2-3;80.
 origin: Aneuploid segregant from T(1;3)w[m49a]/+.
#
Dp(1;3)w[vco] Duplication (1;3) white-variegated cobbled
 cytology: Dp(1;3)2B17-C1;3C4-5;77D3-5;81.
 origin: Aneuploid segregant from T(1;3)w[vco]/+.
#
Dp(1;4)A1: Duplication (1;4) from Austin
 cytology: Dp(1;4)9B;20;101-102.
 origin: Aneuploid segregant from T(1;4)A1/+.
#
Dp(1;4)A12
 cytology: Dp(1;4)1B-C;7A;7B;13B1-5;101-102.
 origin: Aneuploid segregant from T(1;2;4)A12/+.
#
Dp(1;4)N[264-85]: Duplication (1;4) Notch
 cytology: Dp(1;4)3B4-C1;6A2-B1;101F-102A.
 origin: Aneuploid segregant from T(1;2;4)N[264-85].
#
Dp(1;4)N[264-86]
 cytology: Dp(1;4)3C6-7;3E5-6;101F-102.
 origin: Aneuploid segregant from T(1;4)N[264-86]/+.
#
Dp(1;4)r[+] Duplication(1;4) rudimentary-wild type
 origin: X-ray-induced derivative of T(1;4)B[S] =
  T(1;4)16A6-A1;102F2-3; probably a deletion
  of most of the X euchromatin from the
  X[D]4[P] element.
 discoverer: Green.
 references: 1963, Genetica 34: 242-53.
 genetics: Carries normal alleles of r and f appended to
  the right end of chromosome 4.
#
Dp(1;4)w[m51c]: Duplication (1;4) white-mottled
 cytology: Dp(1;4)3C2-3;3C4-7;101.
 origin: Aneuploid segregant from T(1;4)w[m51c]/+.
#
Dp(1;4)w[vD1] Duplication (1;4) white-variegated of Demerec
 cytology: Dp(1;4)3C1-4;101A-D.
 origin: X ray induced in y.
 discoverer: Demerec, 33j19.
 genetics: Variegated for w but not ci. X broken
  between w and rst; 4 probably broken
  in left arm.
#
Dp(1;A)pn-ec Duplication (1;Autosome) prune to echinus
 cytology: Dp(1;A)2D1-2;3F7-4A4;40-41 or 80-81.
 origin: Aneuploid segregant from T(1;A)pn-ec.
#
Dp(1;f)1: Duplication (1;free)
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Muller.
 synonym: Del(1)1.
 references: Painter and Muller, 1929, J. Heredity 20: 287-98.
  Muller and Painter, 1932, Z. Induktive Abstammungs-
  Vererbungslehre 62: 316-65.
 genetics: Contains wild-type alleles of y, sc, br, pn, and
  bb.
#
Dp(1;f)2
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Muller.
 synonym: Del(1)2.
 references: Painter and Muller, 1929, J. Heredity 20: 287-98.
  Muller and Painter, 1932, Z. Induktive Abstammungs-
  Vererbungslehre 62: 316-65.
 genetics: Contains wild-type alleles of y, sc, br, and
  bb.
#
Dp(1;f)3
 cytology: Dp(1;f)1D;19-20 (Gersh) 3.7-4 times the size
  of chromosome 4 at metaphase; lacks only the
  distalmost part of heterochromatic segment hD
  (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
  Grell, 1964, Genetics 50: 151-66.
 genetics: Carries wild-type alleles of y, ac, sc, su(f),
  and bb but not su(w[a]), dor, pn, or
  car. Disjoins regularly from XY, 3%
  nondisjunction from C(1)RM, and causes 18%
  nondisjunction of In(1)dl-49 from + in
  In(1)dl-49/+/Dp(1;f)3 female.
#
Dp(1;f)10
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Carries wild-type alleles of y, ac, and sc
  but not su(f) or bb. Sixty-one percent
  nondisjunction from XY, 45% from C(1)RM, and
  regular disjunction of + from In(1)dl-49 in
  In(1)dl-49/+/Dp(1;f)10 female.
#
Dp(1;f)12
 cytology: 3.4-4 times the size of chromosome 4 at
  metaphase; lacks only the distalmost part of
  heterochromatic segment hD (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Contains wild-type alleles of y, ac, sc,
  su(w[a]), su(f), and bb but not pn or
  car. Disjoins regularly from XY, 4%
  nondisjunction from C(1)RM, and causes 19%
  nondisjunction of + from In(1)dl-49 in
  In(1)dl-49/+/Dp(1;f)12 female.
#
Dp(1;f)14
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Muller.
 synonym: Del(1)14.
 references: Painter and Muller, 1929, J. Heredity 20: 287-98.
  Muller and Painter, 1932, Z. Induktive Abstammungs-
  Vererbungslehre 62: 316-65.
 genetics: Contains wild-type alleles of y, sc, and bb
  but not br.
#
Dp(1;f)18
 cytology: Dp(1;f)1F-2A;19-20 (Gersh).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Contains wild-type alleles of y, ac, sc,
  su(w[a]), and bb but not pn or car.
#
Dp(1;f)24
 cytology: Dp(1;f)1A-B;19-20 (Gersh).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Muller.
 synonym: Del(1)24.
 references: 1932, Proc. Intern. Congr. Genet., 6th.,
  Vol. 1: 213-55.
 genetics: Contains wild-type alleles of l(1)J1, y, and
  ac but not su(w[a]).
#
Dp(1;f)52
 cytology: Dp(1;f)1B10-C4;19-20 (Gersh). 3.7-4 times the
  size of chromosome 4 at metaphase; lacks only
  the distalmost part of heterochromatic segment
  hD (Cooper).
 origin: X-ray-induced deletion of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Contains wild-type alleles of y, ac, sc, su(f),
  and bb but not su(w[a]), pn, or car.
  Segregates normally from XY, 3% nondisjunction
  from C(1)RM, and causes 13% nondisjunction of +
  from In(1)dl-49 in In(1)dl-49/+/Dp(1;f)52.
#
Dp(1;f)60g
 origin: A spontaneous exchange between the distally located
  heterochromatin of In(1)sc[8], y[31d], and
  the proximal heterochromatin of a normal X.
  Occurred in a triploid female.
 discoverer: Mohler, 60g.
 references: 1960, DIS 34: 52.
 genetics: Carries y[31d], ac[+], and su(f)[+] but
  not car[+].
 genetics: The reciprocal product, a reversed acrocentric
  compound X [C(1)RA60g] was recovered from
  the same fly.
#
Dp(1;f)100
 cytology: Two-thirds the length of normal X at metaphase.
 origin: Spontaneous deletion of most of X euchromatin.
 discoverer: L. V. Morgan, 22l.
 synonym: sc-Dp.
 references: 1938, Genetics 23: 423-62.
 genetics: Contains wild-type alleles of y, ac, sc, svr, sta,
  tw, br, pn, fu, car, and bb but not gt, w,
  os, or Bx. Phenotype of duplication-bearing
  female nearly wild type, but occipital bristles and
  hairs are present, eyes are a trifle smaller and
  rougher, and wings have straighter outer margins and
  sometimes scalloped inner margins. In male,
  duplication more than 99% lethal.
#
Dp(1;f)101
 cytology: Dp(1;f)2A2-B1;19F5-20A; one-fourth the length
  of normal X at metaphase.
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Dobzhansky, 1930.
 references: 1932, Tr. Lab. Genet. (Leningrad) 9: 193-216.
  1935, Z. Induktive Abstammungs- Vererbungslehre
  68: 134-62.
 genetics: Contains wild-type alleles of y, sc, svr, su(s),
  dor, and bb but not kz or car
  (Schultz and Bridges, 1932, Am. Naturalist
  66: 323-34; Lewis, 1954, J. Exptl. Zool. 126: 235-75).
  With duplication, both sexes viable and wild type
  except for presence of occipital bristles.
#
Dp(1;f)102
 cytology: One-fifth the length of normal X at metaphase.
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Dobzhansky, 1930.
 references: 1932, Biol. Zentr. 52: 493-509.
  1935, Z. Induktive Abstammungs- Vererbungslehre
  68: 134-62.
 genetics: Contains y[+] to rb[+] inclusive and not
  bb[+]. Usually male lethal, but female
  survives and has occipital bristles, narrow
  parallel-sided wings, branched posterior crossveins,
  and heavier bristles on thorax.
#
Dp(1;f)106
 cytology: Metaphase length about 4 times that of
  chromosome 4.
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Dobzhansky, 1930.
 references: 1932, Biol. Zentr. 52: 493-509.
 genetics: Contains wild-type alleles of y, sc, and svr
  but not bb.
#
Dp(1;f)107
 cytology: Metaphase length about one-fifth that of a normal
  X.
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Dobzhansky, 1930.
 references: 1932, Biol. Zentr. 52: 493-509.
 genetics: Contains wild-type alleles of y, sc, svr, and
  bb.
#
Dp(1;f)112
 cytology: Dp(1;f)1E4-F1;19-20 (Gersh); slightly longer than
  chromosome 4 at metaphase.
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Dobzhansky, 1930.
 references: 1932, Biol. Zentr. 52: 493-509.
 genetics: Contains wild-type alleles of y, sc, svr, and
  su(w[a]) but not bb. Both sexes viable
  and have occipital bristles.
#
Dp(1;f)118
 cytology: About one-fourth the length of normal X at
  metaphase.
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Dobzhansky, 1930.
 references: 1932, Biol. Zentr. 52: 493-509.
 genetics: Contains wild-type alleles of y, sc, svr, and
  bb but not kz.
#
Dp(1;f)122
 cytology: Dp(1;f)1E4-F1;19-20 (Gersh).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Carries wild-type alleles of y, ac, sc, and
  bb but not su(w[a]), pn, car, or
  su(f). Disjoins regularly from XY, 6%
  nondisjunction from C(1)RM, and causes 9%
  nondisjunction of + from In(1)dl-49 in
  In(1)dl-49/+/Dp(1;f)122.
#
Dp(1;f)134
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Dobzhansky, 1931.
 references: 1935, Z. Induktive Abstammungs- Vererbungslehre
  68: 134-62.
 genetics: Contains wild-type alleles of y, sc, svr, and
  br; variegates for y, sc, and svr.
  Both sexes viable and wild type except for presence
  of occipital bristles.
#
Dp(1;f)135
 origin: X-ray-induced deletion of most of X euchromatin
  from y[2].
 discoverer: Dobzhansky, 1930.
 references: Sivertzev-Dobzhansky and Dobzhansky, 1933, Genetics
  18: 173-92.
 genetics: Contains y[2] and wild-type alleles of sc,
  svr, and bb. Both sexes wild type except for
  presence of occipital bristles.
#
Dp(1;f)136
 cytology: Metaphase length about one-fourth that of normal
  X.
 origin: X-ray-induced deletion of most of X euchromatin
  from y[2].
 discoverer: Dobzhansky, 1930.
 references: 1932, Biol. Zentr. 52: 493-509.
 genetics: Contains y[2] and wild-type alleles of sc,
  svr, kz, pn, and bb. Variegates for y
  (Schultz). Viability low. Shows spread wings and
  occipital bristles.
#
Dp(1;f)137
 cytology: About one-fifth the length of normal X at
  metaphase.
 origin: X-ray-induced deletion of most of X euchromatin
  from y[2].
 discoverer: Dobzhansky, 1931.
 references: 1932, Biol. Zentr. 52: 493-509.
 genetics: Contains y[2] through w[+] but not
  bb[+].
#
Dp(1;f)143-3
 origin: Associated with T(1;3)143-3.
#
Dp(1;f)164
 cytology: Dp(1;f)1B;19-20 (Gersh).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Carries wild-type alleles of y and ac but
  not sc, su(w[a]), pn, car, su(f), or bb.
  Disjoins essentially randomly from XY, 36%
  nondisjunction from C(1)RM, and does not
  interfere with disjunction of + from In(1)dl-49
  in In(1)dl-49/+/Dp(1;f)164 female.
#
Dp(1;f)167
 cytology: 3.7-4 times the size of chromosome 4 at
  metaphase; lacks only the distalmost heterochromatic
  segment hD (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Carries wild-type alleles of y, ac, sc,
  su(w[a]), su(f), and bb but not pn or
  car. Disjoins regularly from XY, 3%
  nondisjunction from C(1)RM, and causes 16%
  nondisjunction of + from In(1)dl-49 in
  In(1)dl-49/+/Dp(1;f)167 female.
#
Dp(1;f)179
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Weltman, 1954.
 references: Lindsley and Sandler, 1958, Genetics 43: 547-63.
 genetics: Carries wild-type alleles of y, ac, sc, and
  su(w[a]) but not pn, car, su(f), or
  bb. Disjoins regularly from XY, 20%
  nondisjunction from C(1)RM, and causes 2%
  nondisjunction of + from In(1)dl-49 in
  In(1)dl-49/+/Dp(1;f)179 female.
#
Dp(1;f)749
 cytology: Dp(1;f)1B12-13;20; frequently associated with
  nucleolus in salivary preparations (Krivshenko); 3-4
  times the length of chromosome 4 at metaphase;
  has nucleolus organizer (Cooper).
 origin: X-ray induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1953.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)797
 cytology: Dp(1;f)2B4-5;20; frequently associated with
  nucleolus in salivary preparations (Krivshenko); 2-3
  times the length of chromosome 4 at metaphase;
  has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1953.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)816
 cytology: Invisible in salivary preparations (Krivshenko); 0.7
  the length of chromosome 4 at metaphase; lacks
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of majority of X euchromatin.
 discoverer: Krivshenko and Cooper, 1953.
 references: Grell, 1964, Genetics 59: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, and sc
  but not su(w[a]), dor, pn, su(f), or bb.
  Causes 10% nondisjunction of chromosome 4 when
  added to normal diploid female genotype.
#
Dp(1;f)819
 cytology: Dp(1;f)1D3-4;20; usually associated with
  nucleolus in salivary preparations (Krivshenko); 2.9
  times the length of chromosome 4 at metaphase;
  has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1953.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)856
 cytology: Dp(1;f)1D3-4;20; frequently associated with
  nucleolus in salivary preparations (Krivshenko);
  3 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not su(w[a]), dor, pn, or
  su(f). Causes 2.4% nondisjunction of
  chromosome 4 when added to normal diploid female
  genotype.
#
Dp(1;f)1144
 cytology: Invisible in salivary preparations (Krivshenko); 1.1
  times the length of chromosome 4 at metaphase;
  lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y and ac but
  not sc, svr, su(w[a]), dor, pn, su(f), or
  bb. Causes 36.6% nondisjunction of
  chromosome 4 when added to normal diploid female
  genotype.
#
Dp(1;f)1148
 cytology: Twice the length of chromosome 4 at metaphase;
  has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc, svr, or pn.
#
Dp(1;f)1156
 cytology: 2.6 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1955.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1158
 cytology: 2.3 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1159
 cytology: 2.7 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y and ac but
  not sc or pn.
#
Dp(1;f)1160
 cytology: 3.1 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y and ac but
  not sc or pn.
#
Dp(1;f)1160
 cytology: 3.1 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1955.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1162
 cytology: One-half the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y and ac but not
  sc, su(w[a]), dor, pn, su(f), or bb.
  Causes 3.8% nondisjunction of chromosome 4 when
  added to normal diploid female genotype.
#
Dp(1;f)1170
 cytology: 1.9 times the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y and ac but not
  sc, pn, or bb.
#
Dp(1;f)1173
 cytology: 3.2-3.6 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1185
 cytology: 1.8 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1186
 cytology: 1.6 times the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  of In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y and ac but
  not sc, su(w[a]), dor, pn, su(f), or bb.
  Causes 14.2% nondisjunction of chromosome 4
  when added to normal diploid female genotype.
#
Dp(1;f)1187
 cytology: Less than 0.3 the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y and ac but
  not sc, su(w[a]), dor, pn, su(f), or bb.
  Has no effect on disjunction of chromosome 4
  when added to normal diploid female genotype.
#
Dp(1;f)1191
 cytology: Seven-tenths the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y and ac but
  not sc, pn, or bb.
#
Dp(1;f)1193
 cytology: Same length as chromosome 4 at metaphase; lacks
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y and ac but
  not sc, su(w[a]), dor, pn, su(f), or
  bb. Causes 22.8% nondisjunction of
  chromosome 4 when added to normal diploid
  female genotype.
#
Dp(1;f)1194
 cytology: 3.1 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X
  euchromatin from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb but
  not sc or pn.
#
Dp(1;f)1201
 cytology: 2.2 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1204
 cytology: Nine-tenths the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y and ac but not
  sc, su(w[a]), dor, pn, su(f), or bb.
  Causes 18.9% nondisjunction of chromosome 4 when
  added to normal diploid female genotype.
#
Dp(1;f)1205
 cytology: Seven-tenths the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y but not ac, sc,
  pn, or bb.
#
Dp(1;f)1206
 cytology: One-half the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y but not ac, sc,
  pn, or bb.
#
Dp(1;f)1208
 cytology: Twice the length of chromosome 4 at metaphase;
  has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1209
 cytology: 1.9 times the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin
  from In(1)sc[8].
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, and bb
  but not sc or pn.
#
Dp(1;f)1328
 cytology: Dp(1;f)2A2-3;20; usually associated with
  nucleolus in salivary preparations (Krivshenko); 2.1
  times the length of chromosome 4 at metaphase;
  has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, sc, svr,
  su(w[a]), and bb but not dor, pn, or
  su(f). In(1)sc[4L]sc[8R]/Dp(1;f)1328 dies.
  Causes 3.8% nondisjunction of chromosome 4 when
  added to normal diploid female genotype.
#
Dp(1;f)1330
 cytology: Dp(1;f)2B10-11;20 (Krivshenko); 2.6 times the
  length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1331
 cytology: Dp(1;f)1E-F;20 (Krivshenko); 1.9 times the
  length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1337
 cytology: Dp(1;f)1F4-2A3;19-20 (Gersh; left breakpoint
  originally given as 2B8-9 by Krivshenko); usually
  associated with chromocenter in salivary preparations
  (Krivshenko); 1.4 times the length of
  chromosome 4 at metaphase; lacks nucleolus organizer
  (Cooper).
 origin: X-ray-induced deletion of most of X
  euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, sc,
  su(w[a]), and dor but not pn, su(f), or
  bb. Variegates for dor in male with no
  Y chromosome. Causes 11.9% nondisjunction of
  chromosome 4 when added to normal diploid
  female genotype.
#
Dp(1;f)1339
 cytology: Dp(1;f)1D-E;20; usually associated with
  chromocenter in salivary preparations (Krivshenko);
  1.1 times the length of chromosome 4 at
  metaphase; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  su(w[a]) but not dor, pn, su(f), or
  bb. Causes 17.5% nondisjunction of chromosome 4
  when added to normal diploid female genotype.
#
Dp(1;f)1341
 cytology: Dp(1;f)2C-D;20 (Krivshenko); more than 3 times
  the length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1342
 cytology: More than 3 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 cytology: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1343
 cytology: Dp(1;f)1F;20; usually associated with
  chromocenter in salivary preparations (Krivshenko);
  2.6 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 60: 151-66.
 genetics: Carries wild-type alleles of y, ac, sc, svr,
  su(w[a]), and bb but not dor, pn, or
  su(f).
#
Dp(1;f)1345
 cytology: Dp(1;f)1C;20; always associated with nucleolus
  in salivary preparations (Krivshenko); 1.7 times
  the length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X
  euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1346
 cytology: Dp(1;f)1B12-13;20; usually associated with
  nucleolus in salivary preparations (Krivshenko);
  twice the length of chromosome 4 at metaphase;
  has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1954.
 references: Grell, 1964, Genetics 60: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not su(w[a]), dor, pn, or su(f).
  In(1)sc[4L]sc[8R]/Df(1;f)1346 dies. Causes
  8.6% nondisjunction of chromosome 4 when added
  to normal diploid female genotype.
#
Dp(1;f)1479
 cytology: Dp(1;f)1C;20; usually associated with
  nucleolus in salivary preparations (Krivshenko);
  2.1 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 cytology: Krivshenko and Cooper, 1955.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1488
 cytology: Dp(1;f)2A;20; frequently associated with
  nucleolus in salivary preparations (Krivshenko);
  2.5 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 cytology: Krivshenko and Cooper, 1955.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, sc, svr,
  su(w[a]), and bb but not dor, pn, or
  su(f). Causes 3.8% nondisjunction of
  chromosome 4 when added to normal diploid
  female genotype.
#
Dp(1;f)1489
 cytology: Dp(1;f)1D;20; usually associated with
  nucleolus in salivary preparations (Krivshenko);
  1.8 times the length of chromosome 4 at
  metaphase. Lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1955.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1492
 cytology: Dp(1;f)1B10-12;20; always associated with
  nucleolus in salivary preparations (Krivshenko);
  1.9 times the length of chromosome 4 at
  metapahse; lacks nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1955.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
  In(1)sc[4L]sc[8R]/Dp(1;f)1492 dies.
#
Dp(1;f)1494
 cytology: Dp(1;f)1B10-14;20; usually free of nucleolus
  in salivary preparations (Krivshenko); 2.7 times
  the length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1955.
 genetics: Carries wild-type alleles y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1498
 cytology: Dp(1;f)1F;20; usually free of nucleolus in
  salivary preparations (Krivshenko); 3.3 times the
  length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1955.
 references: Grell, 1964, Genetics 50: 151-66.
  1964, Proc. Natl. Acad. Sci. U.S. 52: 226-32.
 genetics: Carries wild-type alleles of y, ac, sc, svr,
  su(w[a]), and bb but not dor, pn, or
  su(f). Causes 3.2% nondisjunction of
  chromosome 4 when added to normal diploid
  female genotype.
#
Dp(1;f)1501
 cytology: Dp(1;f)2A;19E4-F1; usually free of nucleolus
  in salivary preparations (Krivshenko); 4.4 times
  the length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1956.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1512
 cytology: Dp(1;f)1F;19E4-F1; usually free of nucleolus
  in salivary preparations (Krivshenko); 3.6 times
  the length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1956.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1513
 cytology: Dp(1;f)1B10-14;20; usually associated with
  nucleolus in salivary preparations (Krivshenko);
  more than twice the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1956.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1514
 cytology: Dp(1;f)1B12-13;20; usually associated with the
  nucleolus in salivary preparations (Krivshenko);
  1.9 times the length of chromosome 4 at
  metaphase; has nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1956.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)1518
 cytology: Dp(1;f)2A4-B1;20; usually free of nucleolus in
  salivary preparations (Krivshenko); 3.9 times the
  length of chromosome 4 at metaphase; has
  nucleolus organizer (Cooper).
 origin: X-ray-induced deletion of most of X euchromatin.
 discoverer: Krivshenko and Cooper, 1956.
 genetics: Carries wild-type alleles of y, ac, sc, svr, and
  bb but not pn.
#
Dp(1;f)A1: Duplication (1;free) from Austin
 origin: Aneuploid segregant from T(1;3)A1/+.
#
Dp(1;f)A12
 cytology: Dp(1;f)1B-C;13B1-5.
 origin: Aneuploid segregant from T(1;2;4)A12/+.
#
Dp(1;f)eq Duplication (1;free) from equational producer
 origin: X-ray-induced deletion of most of euchromatin from
  X chromosome carrying eq.
 discoverer: Schultz, 34k4.
 genetics: Contains y[+] to pn[+], inclusive, and
  bb[+]. Male fertile but rather inviable; has
  occipital bristles, eyes rough, wings spread, wing
  veins thickened. Female has occipital bristles;
  wings straight edged and coarse textured. Female with
  two duplications occasionally survives and shows
  extreme spread wings and rough eyes.
#
Dp(1;f)R: Duplication (1;free) from Ring X
 cytology: Dp(1;f)1A3-4;3A;19F-20A1.
 new order:: |1A4 - 3A|20.20F - 20A1|.
 origin: Spontaneous deletion of most of euchromatin from
  R(1)2.
 cytology: Schultz, 35d10.
 synonym: Dp(1;f)X[c2].
 genetics: Covers y to kz but not bb. Variegation
  for dor, ac, svr, pn, and kz; decreased as
  Y's are added. Variegation of y
  insensitive to Y's.
#
Dp(1;f)R1
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])1.
 references: 1942, DIS 16: 65.
#
Dp(1;f)R35
 cytology: Dp(1;f)1A3-4;17A4-5;19F-20A1.
 new order:: |17A5 - 20.20F|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])35.
 references: Slizynska, 1942, DIS 16: 67.
#
Dp(1;f)R36
 cytology: Dp(1;f)1A3-4;17A4-5;19F-20A1.
 new order:: |17A5 - 20.20F|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])36.
 references: Slizynska, 1942, DIS 16: 67.
#
Dp(1;f)R37
 cytology: Dp(1;f)1A3-4;16F2-3;19F-20A1.
 new order:: |16F3 - 20.20F|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])37.
 references: Slizynska, 1942, DIS 16: 67.
#
Dp(1;f)R38
 cytology: Dp(1;f)1A3-4;1F;20.
 new order:: |1A4 - 1F|20.20F -
  20A1|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo, 1942.
 synonym: Del(X[c2])38.
 references: 1942, DIS 16: 65.
#
Dp(1;f)R40
 cytology: Dp(1;f)1A3-4;1F4-5;20.
 new order:: |1A4 - 1F4|20.20F -
  20A1|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])40.
 references: Slizynska, 1942, DIS 16: 67.
#
Dp(1;f)R41
 cytology: Dp(1;f)1A3-4;1F4-5;20.
 new order:: |1A4 - 1F4|20.20F -
  20A1|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])41.
 references: Slizynska, 1942, DIS 16: 67.
#
Dp(1;f)R42
 cytology: Dp(1;f)1A3-4;2A2-3;20.
 new order:: |1A4 - 2A2|20.20F -
  20A1|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])42.
 references: Slizynska, 1942, DIS 16: 67.
#
Dp(1;f)R43
 cytology: Dp(1;f)1A3-4;1F4-5;20.
 new order:: |1A4 - 1F4|20.20F -
  20A1|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 synonym: Del(X[c2])43.
 references: Slizynska, 1942, DIS 16: 67.
#
Dp(1;f)R53d
 cytology: Dp(1;f)1A3-4;1F-2A;20.
 new order:: |1A4 - 1F|20.20F -
  20A1|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: S. Brown, 1953.
 synonym: Del(X[c2])53d.
 references: 1955, DIS 29: 70.
  Brosseau, 1955, DIS 29: 106.
 genetics: Contains wild-type alleles of y, ac, sc, and
  su(s); covers Df(1)260-1. Female
  tolerates two duplications; male tolerates only one.
  Fly hemi- or homozygous for y and the
  duplication shows mosaicism for y. There is
  probably both variegation for y and loss of the
  duplication.
  bb but not pn.
#
Dp(1;f)RA
 cytology: Dp(1;f)1A3-4;1F-2A;20 (Slizynska).
 new order:: |1A4 - 1F|20.20F -
  21A1|.
 origin: X-ray-induced deletion of most of euchromatin from
  R(1)2.
 discoverer: Pontecorvo.
 references: 1942, DIS 16: 65.
#
Dp(1;f)sc[260-27]: Duplication (1;free) scute
 cytology: Dp(1;f)1A8-B1;19F.
 origin: Aneuploid segregant from T(1;2)sc[260-27]/+.
#
Dp(1;f)w[m3]: Duplication (1;free) white-mottled
 cytology: Dp(1;f)3C-D;19-20; breakpoints inferred from
  genetic data.
 origin: X ray induced.
 discoverer: Muller, 1925.
 references: 1930, J. Genet. 22: 299-334.
 genetics: w/Dp(1;f)w[m3] male has variegated eyes and is
  sterile; C(1)RM, w/Dp(1;f)w[m3] female has
  variegated eyes and is fertile.
#
Dp(1;f)y-sc Duplication (1;free) for yellow and scute
 origin: X-ray-induced deletion of most of X euchromatin.
 cytology: Oliver, 32k21.
 references: 1937, DIS 7: 19.
 phenotype: Carries wild-type alleles of y and sc but
  not pn.
#
Dp(1;f)z9: Duplication (1;free) zeste
 cytology: Dp(1;f)3E7-F1;19-20.
 origin: X-ray-induced deletion of most of euchromatin from
  z-bearing X chromosome.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg., Suppl. 38: 1-90
  (fig.).
 genetics: Contains z and wild-type alleles of y through
  dm.
#
Dp(2;1)C239 Duplication (2;1) Crossover suppressor
 cytology: Dp(2;A)7A-B;36C;39E.
 origin: Aneuploid segregant from T(1;2)C239/+.
#
Dp(2;1)OR19 Duplication (2;1) from Oak Ridge
 cytology: Dp(2;1)20;48E;51F;57C.
 origin: Aneuploid segregant from T(1;2)OR19/+.
#
Dp(2;Y)bw[+] Duplication (2;Y) brown-wild type
 cytology: Dp(2;Y)Y[L];58F1-59A2;60E3-F1.
 origin: Aneuploid segregant from T(Y;2)bw[+]Y/+.
#
Dp(2;Y)G
 cytology: Dp(2;Y)36B4-5;40F.
 origin: Aneuploid segregant from T(Y;2)G/+.
#
Dp(2;Y)H
 cytology: Dp(2;Y)37B1-2;40B2-3.
 origin: Aneuploid segregant from T(Y;2)H/+.
#
Dp(2;Y)R24
 cytology: Dp(2;Y)45A;51E.
 origin: Aneuploid segregant from T(Y;2)R24.
#
Dp(2;2)41A
 cytology: Tandem duplication for material in 41A.
 origin: Spontaneous in the In(2L)Cy + In(2R)Cy
  chromosome of a balanced In(2L)Cy +
  In(2R)Cy/M(2)S2[10] stock.
 discoverer: Schultz, 1945.
 genetics: Acts as a suppressor of M(2)S2 and perhaps as a
  partial suppressor of L. Fly heterozygous for
  the duplication appears more stocky than normal.
#
Dp(2;2)bw[AL]Cy[R]
 cytology: Dp(2;2)58A4-B1;59D.
 origin: Associated with In(2R)bw[AL]Cy[R].
#
Dp(2;2)bw[V34kL]Cy[R]
 cytology: Dp(2;2)41;42A2-3.
 origin: Aneuploid recombinant from In(2R)bw[V34k]+Cy/+.
#
Dp(2;2)bw[VDe1L]Cy[R]
 cytology: Dp(2;2)58A4-B1;59E2-4.
 origin: Associated with In(2R)bw[VDe1L]Cy[R].
#
Dp(2;2)bw[VDe2L]Cy[R]
 cytology: Dp(2;2)58A4-B1;59D6-E1.
 origin: Associated with In(2R)bw[VDe2L]Cy[R].
#
Dp(2;2)C619
 cytology: Dp(2;2)26A;28E.
 new order:: 21 - 28E|26A - 60.
 origin: X ray induced in oocyte.
 discoverer: Roberts and Thomas, 1965.
 references: Roberts, 1966, Genetics 54: 969-79.
  Thomas and Roberts, 1966, Genetics 53: 855-62.
 genetics: Homozygous viable. Reduces recombination in 2L.
  Map distance between al and pr reduced from
  44.2 to 7.3 in Dp(2;2)C619/+ and to 17.0 in
  Dp(2;2)C619 homozygotes.
#
Dp(2;2)Cy[L]bw[VDe1R]
 cytology: Dp(2;2)41B2-C1;42A2-3.
 origin: Associated with In(2R)Cy[L]bw[VDe1R].
#
Dp(2;2)Cy[L]bw[VDe2R]
 cytology: Dp(2;2)41A-B;42A2-3.
 origin: Associated with In(2R)Cy[L]bw[VDe2R].
#
Dp(2;2)Cy[R]bw[V34kR]
 cytology: Dp(2;2)58A4-B1;59.
 origin: Aneuploid recombinant from In(2R)bw[V34k]+Cy/+.
#
Dp(2;2)Px[4]: Dp (2;2) Plexate
 cytology: Dp(2;2)60B;60D1-2.
 origin: Associated with In(2LR)S[56f].
#
Dp(2;2)S: Duplication (2;2) Star
 cytology: Dp(2;2)21D2-3;21E2-3; tandem repeat.
 new order:: 21A - 21E2|21D3 - 60.
 origin: Spontaneous as an asymmetrical crossover.
 discoverer: E. B. Lewis, 39i.
 references: 1941, Proc. Natl. Acad. Sci. 27: 31-35.
  1945, Genetics 30: 137-66.
 genetics: Duplicated segment contains the loci of S and
  ast. ast mutant in both members of the
  duplication (+ ast + ast). Duplication
  appears wild type when homozygous or when
  heterozygous with ast. Heterozygous with S,
  it has normal or only slightly roughened eyes.
  Various combinations of S and ast alleles
  have been introduced into the duplication. Through
  unequal crossing over, a triplication and a
  quintuplication of the region have been
  synthesized.
#
Dp(2;2)S[56f]
 cytology: Dp(2;2)21C6-D1;22A3-B1.
 origin: Associated with In(2LR)Px[4].
#
Dp(2;2)SM5
 cytology: Dp(2;2)42A2-3;42D;53C;58A4-B1;58F.
 origin: Associated with In(2LR)SM5.
#
Dp(2;3)C328 Duplication (2;3) Crossover suppressor
 cytology: Dp(2;3)55C;58B;80.
 origin: Aneuploid segregant from T(2;3)C328/+.
#
Dp(2;3)dp: Duplication (2;3) dumpy
 cytology: Dp(2;3)34D;41A;80;81.
 origin: Aneuploid segregant from T(2;3)dp/+.
#
Dp(2;3)P: Duplication (2;3) Pale
 cytology: Dp(2;3)58E3-F2;60D14-E2;96B5-C1.
 origin: Aneuploid segregant from T(2;3)P/+.
#
Dp(2;3)P32: Duplication (2;3) from Pasadena
 cytology: Dp(2;3)41A;42D-E;44C-D;89D7-E1.
 origin: Aneuploid segregant from T(2;3)P32/+.
#
Dp(2;f)1: Duplication (2;free)
 cytology: Dp(2;f)21;41 (left breakpoint tentative)
  superimposed on In(2LR)40F;59E.
 new order:: 21|41 - 40F|59E - 60. Tentative.
 origin: X-ray-induced derivative of In(2LR)bw[V32g];
  possibly a deletion of most of the long arm.
 discoverer: E. H. Grell, 1959.
 genetics: Carries normal alleles of or, sp, bs, Pin, and
  Px but not of al or px.
#
Dp(3;1)N[264-6]: Duplication (3;1) Notch
 cytology: Dp(3;1)3C9-D1;73E;80C.
 origin: Aneuploid segregant from T(1;3)N[264-6]/+.
#
Dp(3;1)O5: Duplication (3;1) of Oliver
 cytology: Dp(3;1)4F2-3;88A-C;92C-D.
 origin: Aneuploid segregant from T(1;3)O5/+.
#
Dp(3;1)ry[35]: Duplication (3;1) rosy
 cytology: Dp(3;1)20;87C-E;91B-C.
 origin: Aneuploid segregant from T(1;3)ry[35]/+.
#
Dp(3;3)bxd[100]: Duplication (3;3) bithoraxoid
 cytology: Dp(3;3)66C;89B5-6;89E2-3.
 origin: Aneuploid recombinant product from
  Tp(3)bxd[100]/+.
#
Dp(3;3)bxd[110]
 cytology: Dp(3;3)89E2-3;91C7-D1;92A2-3.
 origin: Recombinant product from Tp(3)bxd[110]/+.
#
Dp(3;4)ry[+]: Duplication (3;4) rosy-wild type
 cytology: Dp(3;4)86D2-3;88B;101A-D;101F.
 new order:: 88B - 86D3|101F - 101D. Tentative.
 origin: X-ray-induced derivative of the 3R[D]4[P]
  element of T(3;4)86D = T(3;4)86D2-3;101F.
 discoverer: E. H. Grell, 1960.
 references: 1962, Z. Induktive Abstammungs- Vererbungslehre 93: 371-77.
 genetics: Carries normal alleles of cu, kar, and ry.
  Shows tendency toward somatic elimination.
#
In(1)65: Inversion (1) 65
 cytology: In(1)1C;10B.
 origin: X ray induced simultaneously with T(1;3)65 in
  y.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Inseparable from y. About 1% nondisjunction and
  21.8% recombination in In(1)65/+ female; 25.9%
  nondisjunction and 19.7% recombination in
  In(1)65/+/Y female (Grell, 1962, Genetics
  47: 1737-54).
#
In(1)94-2A
 cytology: In(1)1F-2A;5E-6A (Lindsley).
 origin: Derived by recombination from C(1)94-2A.
 discoverer: Rosenfeld.
 genetics: Leads to partial stabilization of tandem ring
  compound X chromosome. Recoverable in
  derivative single ring, R(1)9-4. Exists in
  three interchangeable configurations in the
  C(1)TR (e.g., Novitski and Braver, 1954,
  Genetics 39: 197-209).
#
In(1)272-13
 cytology: In(1)1A6-B1;11A7-8;11F2-12A1;18A4-B1.
 new order:: 1A1 - 1A6|12A1 - 18A4|11A7 -
  1B1|11A8 - 11F2|18B1 - 20.
 origin: X ray induced.
 discoverer: Demerec, 1940.
 references: Sutton, 1943, Genetics 28: 213.
 genetics: Mutant for sc and l(1)272-13 but not ac
  or svr. Male lethal.
#
In(1)303-1
 cytology: In(1)2B13-15;7B1-3;9D1-3.
 new order:: 1 - 2B13|9D1 - 7B3|2B15 - 7B1|9D3
  - 20.
 origin: X ray induced.
 discoverer: Demerec.
 synonym: Tp(1)303-1.
 references: Hoover, 1938, Z. Induktive Abstammungs-
  Vererbungslehre 74: 420-34 (fig.).
 genetics: Nearly lethal.
#
In(1)481
 cytology: In(1)12E-F;14B.
 origin: X ray induced simultaneously with
  Df(1)bb[l-481].
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
#
In(1)A99b: Inversion (1) from Austin
 cytology: In(1)1D3-E1;19D-E.
 origin: X ray induced.
 discoverer: Stone.
 genetics: Viability, fertility, and egg hatch good.
#
In(1)AB
 cytology: In(1)9F;13F1-10.
 discoverer: Bodeman.
 references: Stone and Thomas, 1935, Genetica 17: 170-84.
 genetics: Primary nondisjunction 0.5%, secondary 29.3%;
  recombination 18.2% in In(1)AB/+ and 26.3% in
  In(1)AB/+/Y female (Grell, 1962, Genetics
  47: 1737-54). Stone and Thomas (1935) obtained 14.3%
  recombination in In(1)AB/+.
#
In(1)ac[3]: Inversion (1) achaete
 cytology: In(1)1B2-3;1B14-C1.
 origin: X ray induced.
 discoverer: Dubinin, 1929.
 synonym: In(1)sc[10].
 references: 1930, Zh. Eksperim. Biol. 6: 300-24.
  1932, J. Genet. 25: 163-81.
  1933, J. Genet. 27: 447.
 genetics: Associated with ac[3].
#
In(1)AM
 cytology: In(1)8C17-D1;16E2-3 (Hoover).
 discoverer: Mackensen.
 references: Stone and Thomas, 1935, Genetica 17: 170-84.
  Hoover, 1938, Z. Induktive Abstammungs-
  Vererbungslehre 74: 420-34 (fig.).
 genetics: Homozygous female sterile and therefore used as an
  X chromosome balancer. Inversion departs
  slightly from wild-type phenotype in that eyes are
  rounded and slightly bulging. Total recombination
  3.8% in In(1)AM/+ (Stone and Thomas, 1935).
#
In(1)At: Inversion (1) Attenuated
 cytology: In(1)16A4-5;18C4-6;20A2-3 superimposed on
  In(1)1B3-4;20B-D1[L]1B2-3;20B-D1[R] +
  In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B3|20B - 20A3|16A5 -
  18C4|20A2 - 18C6|16A4 - 11F4|4E1 -
  11F2|4D7 - 1B3|20D1 - 20F.
 origin: X ray induced in In(1)sc[S1L]sc[8R]+dl-49.
 discoverer: Valencia and Valencia, 1949.
 synonym: Tp(1)At.
 references: 1949, DIS 23: 64.
 genetics: Associated with At. Male and homozygous female
  viable and fertile.
#
In(1)B[263-5]: Inversion (1) Bar
 cytology: In(1)15F9-16A1;16A7-B1;17A3-4. Left break
  occurs between repeated regions associated with
  Dp(1;1)B = Dp(1;1)15F9-16A1;16A7-B1 (Kaufmann and
  Sutton).
 new order:: 1 - 16A7|17A3 - 16A1|17A4 - 20.
 origin: X ray induced in B.
 discoverer: Demerec, 33k.
 references: Sutton, 1943, Genetics 28: 97-107.
 genetics: B reversed; lethal; un, vb, f, lh, and
  os[o] not affected.
#
In(1)B[263-24]
 cytology: In(1)10C2-D1;12D2-E1;15F9-16A1;16A7-B1; right
  breakpoint between first and second segments of
  B[i]B[i] triplication.
 new order:: 1 - 10C2|16A7 - 12E1|10D1 -
  12D2|16A1 - 16A7|16A1 - 20.
 origin: X ray induced in Dp(1;1)B[i]B[i] =
  Dp(1;1)15F9-16A1;16A7-B1.
 discoverer: Demerec, 34a.
 synonym: Tp(1)B[263-24].
 references: Sutton, 1943, Genetics 28: 97-107.
 genetics: Reversal of B[i]B[i] to wild type; un, vb,
  f, lh, and os not affected. Male lethal.
#
In(1)B[263-47]
 cytology: In(1)16A2-4;20A2-3.
 origin: X ray induced.
 discoverer: Demerec, 38d.
 references: Sutton, 1943, Genetics 28: 97-107.
 genetics: Position effect at B.
#
In(1)B[M1]: Inversion (1) Bar of Muller
 cytology: In(1)16A2-5;20A3-B (Sutton, 1943, Genetics
  28: 97-107).
 origin: X ray induced.
 discoverer: Muller, 34e.
 references: 1935, DIS 3: 29.
 genetics: Position effect at B. Primary nondisjunction
  0.4 and secondary 18.5%; recombination 32% in
  In(1)B[M1]/+ and 35.4% in In(1)B[M1]/+/Y
  female (Grell, 1962, Genetics 47: 1737-54).
#
In(1)B[M2]
 cytology: In(1)16A2-5;20E (Sutton, 1943, Genetics 28: 97-107).
 origin: X ray induced.
 discoverer: Muller, 34e.
 references: 1935, DIS 3: 29.
 genetics: Position effect at B.
#
In(1)B[rev-2]: Inversion (1) Bar-reversed
 cytology: In(1)3F8-4A1;16A2-4; right break in right
  section of Dp(1;1)B = Dp(1;1)15F9-16A1;16A7-B1.
 new order:: 1 - 3F8|16A2 - 16A1|16A7 -
  4A1|16A4 - 20.
 origin: X ray induced in Dp(1;1)B.
 discoverer: Bishop, 1940.
 references: Sutton, 1943, Genetics 28: 100.
 genetics: Reversal of B.
#
In(1)B[rev-3]
 cytology: In(1)15F9-16A1;16A7-B1;20A5-B1; right break
  between segments of Dp(1;1)B =
  Dp(1;1)15F9-16A1;16A7-B1.
 new order:: 1 - 16A7|20A5 - 16A1|20B1 - 20F.
 origin: X ray induced in B.
 discoverer: Bishop, 1940.
 references: Sutton, 1943, Genetics 28: 100.
 genetics: B reversion.
#
In(1)bb[Df]: Inversion (1) bobbed-Deficiency
 cytology: In(1)4D2-3;20B-C;20C-D; deficient for 20C-D;
  two-thirds normal length at metaphase.
 new order:: 1 - 4D2|20B - 4D3|20D - 20F.
 origin: X ray induced.
 discoverer: Sivertzev-Dobzhansky and Dobzhansky, 31b.
 references: 1933, Genetics 18: 173-92.
  Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Right breakpoint between rb and rg.
  Deficient for bb. In(1)bb[Df]/+ female
  produces about 2% exceptional sons from 4-strand
  double exchange within inverted segment. Secondary
  exceptions about 13%.
#
In(1)bb[DfL]Cl[R] Inversion (1) bobbed-Deficiency Left Cl-Right
 cytology: In(1)4D2-3;20B-C[L]4A5-B1;17A6-B1[R];
  duplicated for 4B1-D2 and 17B1-20B.
 origin: Recombinant containing left end of In(1)bb[Df]
  and right end of In(1)Cl.
 references: Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Duplicated for bi, rb, fu, and car but not
  ec, rg, f, os, or bb. Survives as small
  male with less convex outer wing margins than normal
  and usually one or more notches at wing tips;
  sterile, has collapsed testes. Heterozygous female
  fertile, has slightly narrowed wings.
#
In(1)bb[DfL]y[4R] Inversion (1) bobbed-Deficiency Left yellow-4 Right
 cytology: In(1)4D2-3;20B-C[L]1A8-B1;18A3-4[R];
  duplicated for 1B1-4D2 and 18A4-20B.
 origin: Recombinant containing left end of In(1)bb[Df]
  and right end of In(1)y[4].
 references: Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Duplicated for ac through rb and fu
  through car. Heterozygous female has stubby
  posterior verticals and disarranged scutellars; outer
  wing margin less convex than normal; fair viability
  and fertility. Enhances expression of heterozygous
  B. Male lethal.
#
In(1)Br: Inversion (1) Bridged
 origin: X ray induced.
 discoverer: Muller, 27l3.
 references: 1935, DIS 3: 29.
 genetics: Associated with dominant mutant, Br. Crossing
  over suppressed to right of v, about normal to
  left.
#
In(1)C18: Inversion (1) Crossover suppressor
 cytology: In(1)3F;17A1-6.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Eliminates sc-f recombination. Male viable.
#
In(1)C146
 cytology: In(1)1F;14A.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Eliminates sc-f recombination. Male fertile.
#
In(1)C206
 cytology: In(1)8F;11A;16A.
 new order:: 1 - 8F|16A - 11A|8F - 11A|16A -
  20.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Eleven percent recombination between sc and
  f. Male lethal.
#
In(1)Cl: Inversion (1) Cl
 cytology: In(1)4A5-B1;17A6-B1 (Hoover, 1938, Z. Induktive
  Abstammungs- Vererbungslehre 74: 429).
 origin: Spontaneous in a sc t[2] v sl B chromosome.
 discoverer: Muller, 20j.
 references: 1928, Genetics 13: 279-357.
  Gershenson, 1935, J. Genet. 30: 115-25.
  Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Left break between ec and bi; right break
  between os and fu; l(1)C associated
  with left break x ller). About 0.35% primary and
  37% secondary exceptions. Total recombination about
  1%.
 genetics: In(1)Cl, sc l(1)C t[2] v sl B is the ClB
  chromosome, described in the section on balancers.
#
In(1)Cl[L]bb[DfR] Inversion (1) Cl-Left bobbed-Deficiency Right
 cytology: In(1)4A5-B1;17A6-B1[L]4D2-3;20C-D[R];
  deficient for 4B1-D2 and 17B1-20C.
 origin: Recombinant containing left end of In(1)Cl and
  right end of In(1)bb[Df].
 references: Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Deficient for bi, rb, fu, car, and bb but not
  ec, rg, f, or os. Both bi and fu
  lethal when heterozygous for
  In(1)Cl[L]bb[DfR]. Heterozygous female
  extreme Minute [M(1)4BC + M(1)n], with
  abnormal wing shape; ovaries normal but female
  sterile. Male lethal.
#
In(1)Cl[L]y[4R] Inversion (1) Cl-Left yellow-4 Right
 cytology: In(1)4A5-B1;17A6-B1[L]1A8-B1;18A3-4[R];
  duplicated for 1B1-4A5, deficient for 17B1-18A3.
 origin: Recombinant containing left end of In(1)Cl and
  right end of In(1)y[4].
 references: Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Duplicated for ac through ec; deficient
  for fu but not f, vb, os, or car.
  Heterozygous female has irregular acrostichal rows
  and wings smaller and with less-convex posterior
  margin than normal. Enhances expression of
  heterozygous B. Male lethal.
#
In(1)ct[3a2]: Inversion (1) cut
 cytology: In(1)7B2-C1;19-20.
 origin: X ray induced.
 discoverer: Hannah, 47g.
 genetics: ct affected but not cm, sn, or oc. Male
  lethal.
#
In(1)ct[3b1]
 cytology: In(1)3A4-B1;7B2-5. May be a duplication for
  3A3-4 or insertion of material from another
  chromosome.
 origin: X ray induced.
 discoverer: Hannah, 47g.
 genetics: ct affected but not pn, w, cm, sn, or
  oc. Male lethal.
#
In(1)ct[12a2]
 cytology: In(1)4E2-3;7B2-4 (Hannah).
 origin: X ray induced.
 discoverer: De Frank, 47g.
 genetics: ct affected but not rb, cx, rg, cm, sn, or
  oc. Male lethal.
#
In(1)ct[13a1]
 cytology: In(1)7B2-3;19-20.
 origin: X ray induced.
 discoverer: Hannah, 47g.
 genetics: ct affected but not cm, sn, or oc. Male
  lethal.
#
In(1)ct[14a3]
 cytology: In(1)7B2-3;20; position of heterochromatic
  breakpoint with respect to centromere unknown.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 14a3.
 genetics: ct affected but not y, ac, sc, cm, sn, or
  oc. Male lethal.
#
In(1)ct[14b2]
 cytology: In(1)3D2-5;7B2-4.
 origin: X ray induced.
 discoverer: Hannah, 47g.
 genetics: ct affected but not cm, sn, or oc. Male
  lethal.
#
In(1)ct[43aH1]
 cytology: In(1)4B1-4;7B4-C1 + In(1)10D5-6;20B-C.
 origin: X ray induced.
 discoverer: Muller, Valencia, and Valencia, 1946-53.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Associated with ct[43aH1].
#
In(1)ct[268-13]
 cytology: In(1)2E3-F1;2F2-3;7B2-3;7B4-5;19A4-5;19A6-B1
  superimposed on R(1)1A3-4;19F-20A1. 2F1-2,
  7B3-4, and 19A5-6 missing.
 new order:: |1A4 - 2E3|7B2 - 2F3|19A4 -
  7B5|19B1 - 20.20 -
  20A1|.
 origin: X ray induced in R(1)2.
 discoverer: Demerec, 34f.
 references: Hoover, 1937, Genetics 22: 634-40 (fig.).
  1938, Z. Induktive Abstammungs- Vererbungslehre
  74: 420-34 (fig.).
 genetics: Deficient for ct but not scp or sn. Male
  lethal.
#
In(1)ct[268-18]
 cytology: In(1)7B2-3;7B4-5;11D8-9; 7B3-4 missing.
 new order:: 1A - 7B2|11D8 - 7B5|11D9 - 20.
 origin: X ray induced.
 discoverer: Hoover, 1938.
 references: 1938, Z. Induktive Abstammungs- Vererbungslehre
  74: 420-34 (fig.).
 genetics: Deficient for ct but not scp or sn.
  Male lethal.
#
In(1)ct[268-20]
 cytology: In(1)6F11-7A1;7B5-6;10B11-12. 7A1-B5 missing.
 new order:: 1 - 6F11|10B11 - 7B6|10B12 - 20.
 origin: X ray induced.
 discoverer: Demerec, 35g.
 references: Hoover, 1938, Z. Induktive Abstammungs-
  Vererbungslehre 74: 420-34 (fig.).
 genetics: Deficient for ct but not cm, scp, or sn.
  Male lethal.
#
In(1)ct[268-27]
 cytology: In(1)3D6-E1;7B3-5.
 origin: X ray induced.
 discoverer: Hoover, 35j.
 references: 1938, Z. Induktive Abstammungs- Vererbungslehre
  74: 420-34 (fig.).
 genetics: ct affected but not cm, scp, or sn.
  Male lethal.
#
In(1)D1: Inversion (1) from deoxycytidine
 cytology: In(1)13B;16A.
 origin: Induced by tritiated deoxycytidine.
 discoverer: Kaplan, 1965.
 references: 1966, DIS 41: 59.
 genetics: Male lethal.
#
In(1)dl-49: Inversion (1) delta-49
 cytology: In(1)4D7-E1;11F2-4 [Painter; Hoover, 1938,
  Z. Induktive Abstammungs- Vererbungslehre 74: 420-34
  (fig.)].
 discoverer: Muller, 26k.
 references: Muller and Stone, 1930, Anat. Record 47: 393-94.
  Stone and Thomas, 1935, Genetica 17: 170-84.
  Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Left break between rb and cv; right between
  fw and g. Measures of recombination vary
  from 5.5% (Grell, 1962, Genetics 47: 1737-54) to
  about 15% (Sturtevant and Beadle, 1936); secondary
  exceptions from 33% (Grell, 1962) to 44% (Sturtevant
  and Beadle, 1936).
 genetics: Used as a balancer either with markers y Hw m[2]
  g[4] or y w lz[s] with Hw and
  lz[s] sterilizing homozygous female.
#
In(1)drp: Inversion (1) droop wings
 cytology: In(1)12B;20B.
 origin: Spontaneous from hi.
 discoverer: Ives, 48f.
 synonym: In(1)hi1; Inversion (1) droop.
 references: 1949, DIS 23: 58.
 genetics: Associated with mutant droop wings. Male viable.
#
In(1)dta: Inversion (1) delta wing
 cytology: In(1)6B2-3;15E7-F2.
 origin: Induced by triethylenemelamine (CB. 1246).
 discoverer: Fahmy, 1953.
 references: 1958, DIS 32: 69.
 genetics: Associated with dta. Female sterile.
#
In(1)e(bx): Inversion (1) enhancer of bithorax
 cytology: In(1)3A;4F.
 origin: Gamma ray induced.
 discoverer: E. B. Lewis, 53b.
 references: 1959, DIS 33: 96.
 genetics: Associated with e(bx).
#
In(1)EN: Inversion (1) Entire
 cytology: In(1)1A;20;20B-C. At prophase, distal end
  carries a single heterochromatic segment about equal
  in size to chromosome 4; proximally, it
  carries a very short heterochromatic segment and as
  a second arm two larger heterochromatic segments
  (Lindsley).
 new order:: 20 - 1A|20C - 20F.20.
  Tentative.
 origin: Spontaneous opening out of R(1)1, y.
 discoverer: Novitski.
 references: 1949, DIS 23: 94-95.
  Lindsley, 1958. Z. Induktive Abstammungs- Vererbungslehre
  89: 103-22.
 genetics: Entire chromosome, including l(1)J1[+] and
  y, inverted. Carries mutant alleles of bb
  at each end, which acting together produce
  bb[+] phenotype.
#
In(1)EN2
 cytology: In(1)1A3-4;19F-20A1;20. Inferred from origin.
 new order:: 20 - 1A3|20A1 - 20F.20.
  Tentative.
 origin: Spontaneous opening of R(1)2, y[+].
 discoverer: Muller.
 references: 1956, DIS 30: 140-41.
 genetics: Entire chromosome inverted like In(1)EN but
  carries y[+] rather than y.
#
In(1)EN2B: Inversion (1) Entire 2 of Bender
 cytology: In(1)1A3-4;19F-20A1;20. Inferred from origin.
 new order:: 20 - 1A3|20A1 - 20F.20.
  Tentative.
 origin: Spontaneous opening of R(1)2, y v.
 discoverer: M. A. Bender, 55e6.
 references: 1955, DIS 29: 69.
#
In(1)exr: Inversion (1) extra venation
 cytology: In(1)12E8-10;15D1-3.
 origin: Induced by triethylenemelamine (CB. 1246).
 cytology: Fahmy, 1952.
 references: 1958, DIS 32: 70.
 genetics: Affects exr.
#
In(1)f[257-4]: Inversion (1) forked
 cytology: In(1)15F2-16A1;16D2-E1.
 origin: X ray induced.
 discoverer: Demerec, 33j.
 genetics: f affected.
#
In(1)FM3: Inversion (1) First Multiple
 cytology: In(1)3E-F;16A-B;19F-20B; superimposed on
  In(1)1B2-3;20B-D1 + In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B2|20B|16B - 19F|3F -
  4D7|11F2 - 4E1|11F4 - 16A|3E -
  1B3|20D1 - 20F.
 origin: X ray induced in In(1)sc[8]+dl-49, y[31d]
  s[8] dm B.
 discoverer: R. F. Grell, 1954.
 references: Mislove and Lewis, 1954, DIS 28: 77.
 genetics: Mutant for two lethals, one allelic to l(1)J1 and
  therefore covered by y[+]Y and the other
  covered by B[S]Y; both
  In(1)FM3/y[+]Y/B[S]Y and In(1)FM3/B[S]Y
  y[+] males survive. The treated chromosome
  carried y[31d], but In(1)FM3/y variegates
  for yellow bristles.
 genetics: Used as a first chromosome balancer, described as
  FM3 in the section on balancers.
#
In(1)FM4
 cytology: In(1)3C;4E-F superimposed on In(1)1B2-3;20B-D1
  + In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B2|20B - 11F4|4E|3C -
  4D7|11F2 - 4F|3C - 1B3|20D1 - 20F.
 origin: X ray induced in In(1)sc[8]+dl-49, y[31d]
  sc[8] dm B.
 discoverer: R. F. Grell, 1954.
 references: Mislove and Lewis, 1954, DIS 28: 77.
 genetics: Male viable and fertile.
 genetics: Used as a first chromosome balancer, described as
  FM4 in the section on balancers.
#
In(1)FM6
 cytology: In(1)15D-E;20A-B superimposed on
  In(1)1B2-3;20B-D1 + In(1)3C;4E-F +
  In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B2|20B|15E - 20A|15D -
  11F4|4E|3C - 4D7|11F2 - 4F|3C -
  1B3|20D1 - 20F.
 origin: X ray induced in In(1)FM4, y[31d] sc[8] dm B.
 discoverer: R. F. Grell, 55i.
 references: Grell and Lewis, 1956, DIS 30: 70.
 genetics: Male viable and fertile. Female sterile owing to
  dm.
 genetics: Used as first chromosome balancer, described as
  FM6 in the section on balancers.
#
In(1)g[17Ba6]: Inversion (1) garnet
 cytology: In(1)12B14-15;19F superimposed on
  In(1)1B3-4;20B-D1[L]1B2-3;20B-D1[R] +
  In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B3|20B - 19F|12B15 -
  19F|12B14 - 11F4|4E1 - 11F2|4D7 -
  1B3|20D1 - 20F.
 origin: X ray induced in In(1)sc[S1L]sc[8R]+dl-49.
 discoverer: Muller, Valencia, and Valencia, 1946-53.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Associated with g[17Ba6].
#
In(1)g[w]: Inversion (1) garnet-wild
 cytology: Breakpoints unknown.
 origin: X ray induced.
 discoverer: Muller.
 references: 1946, DIS 20: 67.
  Chovnick, 1958, DIS 32: 88.
  1961, Genetics 46: 493-507 (fig.).
 genetics: Associated with g[w].
#
In(1)g[X]: Inversion (1) garnet from X irradiation
 cytology: In(1)12;19-20.
 origin: X ray induced.
 discoverer: Muller.
 references: 1946, DIS 20: 67.
 genetics: Mutant for g.
#
In(1)hi2: Inversion (1) from high
 cytology: In(1)1F;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi3
 cytology: In(1)4D;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi4
 cytology: In(1)4C;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution: 19-28.
 genetics: Male lethal.
#
In(1)hi5
 cytology: In(1)1F;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi7
 cytology: In(1)12E;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi8
 cytology: In(1)3C;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi9
 cytology: In(1)8F;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi10
 cytology: In(1)4E2-3;8A1-2.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi11
 cytology: In(1)5C;7E;20A-F.
 new order:: 1 - 5C|7E - 20A|7E - 5C|20F.
 origin: Recovered among progeny of Florida high.
 discoverer: Ives.
 synonym: Tp(1)hi11.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi12
 cytology: In(1)1C3;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)hi13
 cytology: In(1)4E;20.
 origin: Spontaneous in hi.
 discoverer: Ives.
 references: Hinton, Ives, and Evans, 1952, Evolution 6: 19-28.
 genetics: Male lethal.
#
In(1)Hv: Inversion (1) Hooked veins
 cytology: Breakpoints unknown.
 discoverer: Tanaka, 35a4.
 references: 1937, DIS 8: 11.
 genetics: Associated with Hv.
#
In(1)Hw[2]: Inversion (1) Hairy wing
 cytology: In(1)1A2-3;1A8-B1;1B2-3.
 new order:: 1A1 - 1A2|1B2 - 1A3|1B1 - 20.
 origin: Spontaneous derivative of Dp(1;1)Hw =
  Dp(1;1)1A8-B1;1B2-3.
 discoverer: Nichols-Skoog, 35a9.
 genetics: Associated with Hw[2].
#
In(1)K2: Inversion (1) of Krivshenko
 cytology: In(1)6A;9A-B.
 origin: Spontaneous.
 discoverer: Krivshenko, 54c24.
 references: 1956, DIS 30: 75.
 genetics: Homozygous viable.
#
In(1)l-272-13: Inversion (1) lethal
 cytology: In(1)1A6-B1;11A7-8;11F2-12A1;18A4-B1.
 new order:: 1A1 - 1A6|12A1 - 18A4|11A7 -
  1B1|11A8 - 11F2|18B1 - 20.
 origin: X ray induced.
 discoverer: Demerec, 1940.
 synonym: Tp(1)l-272-13.
 references: Sutton, 1943, Genetics 28: 210-17.
 genetics: Associated with l(1)271-13. sc affected but not
  y, ac, or svr.
#
In(1)l-v59: Inversion (1) lethal-variegated
 cytology: In(1)3-4;19-20.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male fertile.
#
In(1)l-v132
 cytology: In(1)4E;19-20.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male fertile.
#
In(1)l-v146
 cytology: In(1)5-6;19-20.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male fertile.
#
In(1)l-v227
 cytology: In(1)1-2;19-20.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male fertile.
#
In(1)l-v231
 cytology: In(1)1C-D;19-20.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Vareigated for a lethal; male fertile.
#
In(1)l-zw1[g31]: Inversion (1) lethal-zeste white
 cytology: In(1)3A;6.
 origin: X ray induced.
 discoverer: Judd, 62g31.
 genetics: Mutant for l(1)zw1.
#
In(1)l-zw3[b12]
 cytology: In(1)3A8-B1;13.
 origin: X ray induced.
 discoverer: Judd, 62b12.
 genetics: Mutant for l(1)zw3.
#
In(1)lz[sB] Inversion (1) lozenge-spectacled of Bishop
 cytology: In(1)8;20 (Green).
 origin: X ray induced.
 discoverer: Bishop.
 references: Oliver, 1947, Texas Univ. Publ. 4720: 167-84.
 genetics: Associated with lz[sB].
#
In(1)lz1: Inversion (1) lozenge
 cytology: In(1)8D;20D
#
In(1)vao: Inversion (1) varied outspread
 cytology: In(1)18C5-6;19E7-8.
 origin: Induced by triethylenemelamine (CB. 1246).
 discoverer: Fahmy, 1953.
 references: 1959, DIS: 33: 94.
 genetics: Mutant for vao; variegated for an eye color,
  possibly car. Male sterile.
#
In(1)w[258-52]: Inversion (1) white
 cytology: In(1)3C7-9;8E11-8F1 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 40a.
 genetics: Mutant for w and rst but not for spl, lz,
  dvr, or flp.
#
In(1)w[G]: Inversion (1) white of Goldschmidt
 cytology: In(1)3C;3D-E (Kodani).
 origin: X ray induced in In(1)y[G] = In(1)1A;1C3-4.
 discoverer: Goldschmidt.
 references: 1945, Univ. Calif. (Berkeley) Publ. Zool 49: 522.
#
In(1)w[m4]: Inversion (1) white-mottled
 cytology: In(1)3C1-2;20A (Sutton). Right breakpoint in
  mitotic chromosomes is to the left of bb in
  hC or hD (Cooper, 1959, Chromosoma 10: 535-88).
 origin: X ray induced.
 discoverer: Muller, 1929.
 references: 1930, J. Genet. 22: 299-334.
 genetics: Variegated for w. Left break to the left of
  w.
#
In(1)w[m4L]rst[3R] Inversion (1) white-mottled 4 Left roughest-3 Right
 cytology: In(1)3C1-2;20A[L]3C3-4;20B[R] deficient
  for 3C1-2.
 origin: Recombinant containing left end of In(1)w[m4]
  and right end of In(1)rst[3].
 genetics: Deficient for w and l(1)3C3 but not rst
  (Lefevre and Wilkins, 1966, Genetics 53: 175-87).
#
In(1)w[m4L]w[mJR] Inversion (1) white-mottled 4 Left white-mottled of Jonsson Right
 cytology: In(1)3C1-2;20A[L]3C2-3;20[R]; deficient
  for 3C2 and for an undetermined portion, including
  the centromere, of the base of the X.
 new order:: 1 - 3C1|20A - 3C3|102C - 101A.
 origin: Recombinant containing left end of In(1)w[m4]
  and right end of In(1)w[mJ], which is part of
  T(1;4)w[mJ].
 references: Lefevre, 1963, DIS 37: 49-50.
  Lefevre and Wilkins, 1966, Genetics 53: 175-87.
 genetics: Deficient for white; male viable and therefore not
  deficient for l(1)3C3. Also deficient for
  proximal heterochromatin, probably including bb.
#
In(1)w[m51b]
 cytology: In(1)3C1-2;20; right break proximal to the
  nucleolus organizer (Gersh).
 origin: X ray induced.
 discoverer: Baker, 51b19.
 genetics: Variegated for w and rst. Recombinant
  carrying left end of In(1)w[m51b] and right
  end of the 4-centric element of T(1;4)w[mJ]
  = T(1;4)3C2-3;20;102C is white eyed and male
  viable, indicating that In(1)w[m51b], like
  In(1)w[m4] = In(1)3C1-2;20A, is broken between
  3C1 and 2 (Gersh).
#
In(1)w[m53j]
 cytology: In(1)1A;3C3-5;20;20B-C;20C-F. Inferred from
  origin.
 new order:: 20 - 3C5|20C|1A -
  3C3|20F.20.
  Tentative.
 origin: X ray induced in In(1)EN = In(1)1A;20;20B-C.
 discoverer: M. A. Bender, 53j.
 references: 1955, DIS 29: 69.
 genetics: Variegated for w.
#
In(1)w[m54l]
 cytology: In(1)3C3-5;20D.
 origin: Neutron induced.
 discoverer: Mickey, 54l3.
 references: 1963, DIS 38: 29.
 genetics: Variegated for w.
#
In(1)w[m55b]
 cytology: In(1)1A3-4;3C3-5;20;19F-20A1;20A1-F. Inferred
  from origin. Appears as a rod in metaphase.
 new order:: 20 - 3C5|20A1|1A4 -
  3C3|20F.20.
  Tentative.
 origin: X-ray-induced derivative of R(1)2 =
  R(1)1A3-4;19F-20A1 opened in inverted order.
 discoverer: M. A. Bender, 55b28.
 references: 1955, DIS 29: 69.
 genetics: Variegated for w.
#
In(1)w[mJ]: Inversion (1) white-mottled of Jonsson
 cytology: In(1)3C2-3;20.
 origin: Associated with T(1;4)w[mJ] =
  T(1;4)3C2-3;20;102C.
#
In(1)w[mJL]rst[3R] Inversion (1) white-mottled of Jonsson Left roughest-3 Right
 cytology: In(1)3C2-3;20[L]3C3-4;20B[R]; deficient
  for 3C3.
 origin: Recombinant carrying left end of In(1)w[mJ],
  which is part of T(1;4)w[mJ], and right end of
  In(1)rst[3].
 references: Lefevre, 1963, DIS 37: 49-50.
  Lefevre and Wilkins, 1966, Genetics 53: 175-87.
 genetics: Deficient for l(1)3C3 but not w.
#
In(1)w[mMc] Inversion (1) white-mottled of McLean
 cytology: In(1)3C1-2;20A-C; inferred from genetic data.
 origin: X ray induced.
 discoverer: McLean.
 references: Muller, 1946, DIS 20: 68.
 genetics: Variegates for w and rst. Complementary
  single recombinants between In(1)w[m4] =
  In(1)3C1-2;20A and In(1)w[mMc] are viable,
  fertile, and bb[+]. Left breakpoints therefore
  identical and right breakpoints on the same side of
  bb.
#
In(1)w[vC] Inversion (1) white-variegated of Catcheside
 cytology: In(1)3C1-2;19-20 superimposed on
  R(1)1A3-4;19F-20A1.
 new order:: |1A4 - 3C1|19 -
  3C2|20.20F - 20A1|.
 origin: X ray induced in R(1)2.
 discoverer: Catcheside.
 references: Hinton, 1955, Genetics 40: 952-61.
 genetics: Variegates for w, rst, spl, and N but not
  y. X/Y male viability reduced; X/Y/Y male
  more viable. Characterized by variable degree of
  instability manifested by production of
  gynandromorphs, X/0 males, and dominant lethals.
  An extreme example gave 140 females, 106 gynandromorphs,
  181 X/0 males, and 868 dominant
  lethals among 1295 putative ring/rod zygotes. Small
  ring-shaped duplications are generated infrequently
  (analysis by Hinton, 1955). Behavior of rod
  derivatives of In(1)w[vC] (Hinton, 1957,
  Genetics 42: 55-65) suggests generation of
  dicentrics through sister-strand fusion rather than
  exchange. Fusion postulated to occur in
  heterochromatin of the 3C1|19 reunion point of
  In(1)w[vC]. Mitotic abnormalities in cleavage
  of In(1)w[vC] embryos described (Hinton, 1959,
  Genetics 44: 923-31). Chromosome tends to become
  stable in stocks. Viability and fertility
  correlated with stability.
#
In(1)y[3P]: Inversion (1) yellow-3 of Patterson
 cytology: In(1)1A;20. Reported as In(1)1B1-2;20 by
  Muller and Prokofyeva (1935), but this is
  contradictory to subsequent observations placing
  y in 1A.
 origin: X ray induced.
 discoverer: Patterson, 31e25.
 references: Muller, 1935, Genetica 17: 237-52.
  Muller and Prokofyeva, 1935, Proc. Natl. Acad. Sci. U.S. 21: 16-26.
  Sidorov, 1936, Biol. Zh. (Moscow) 5: 3-26.
 genetics: Variegated for y and, to a lesser extent, for
  Hw. Genetics breaks between l(1)J1 and
  y and between bb and centromere. Inversion
  slightly longer than In(1)sc[8].
#
In(1)y[3PL]sc[8R] Inversion (1) yellow-3 of Patterson Left scute-8 Right
 cytology: In(1)1A;20[L]1B2-3;20B-D1[R]; deficient for
  1A-B2.
 origin: Recombinant containing left end of In(1)y[3P]
  and right end of In(1)sc[8].
 references: Muller, 1935, J. Heredity 26: 469-78.
 genetics: Deficient for y and ac but not l(1)J1,
  sc, or bb. Male viable.
#
In(1)y[4]
 cytology: In(1)1A8-B1;18A3-4 (Norton and Valencia, 1965,
  DIS 40: 40).
 origin: X ray induced.
 discoverer: Serebrovsky.
 references: Dubinin and Friesen, 1932, Biol. Zentr. 52: 147-62.
  Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Mutant for y. Right break between l(1)J1 and
  ac; left break between fu on left and
  sby, smd, and coc on right; shown by
  deficiency of In(1)y[4L]sc[9R] for ac, sby,
  smd, and coc but not l(1)J1 or fu
  (Norton and Valencia, 1965). In(1)y[4]/+
  female produces about 2% exceptional sons from
  4-strand double exchange in the inverted regions;
  In(1)y[4]/+/Y female produces about 7% secondary
  exceptions (Sturtevant and Beadle, 1936).
#
In(1)[y4L]sc[4R] Inversion (1) yellow-4 Left scute-4 Right
 cytology: In(1)1A8-B1;18A3-4[L]1B3-4;19F-20C1[R];
  deficient for 1B1-3 and 18A4-19F.
 origin: Recombinant containing left end of In(1)y[4] and
  right end of In(1)sc[4].
 references: Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Deficient for ac, sc, car, and M(1)n but not
  pn, rst, or os. Heterozygous female Minute
  and poorly viable but fertile. Male lethal.
#
In(1)[y4L]sc[8R] Inversion (1) yellow-4 Left scute-8 Right
 cytology: In(1)1A8-B1;18A3-4[L]1B2-3;20B-D1[R];
  deficient for 1B1-2 and 18A4-20B.
 origin: Recombinant containing left end of In(1)y[4] and
  right end of In(1)sc[8].
 references: Sturtevant and Beadle, 1936, Genetics 21: 554-604.
 genetics: Deficient for ac, car, M(1)n, and bb but not
  svr; either deficient for y or carries
  y[4]. Heterozygous female Minute, fertile,
  and poorly viable. Male lethal.
#
In(1)[y4L]sc[9R] Inversion (1) yellow-4 Left scute-9 Right
 cytology: In(1)1A8-B1;18A3-4[L]1B2-3;18B8-9[R];
  deficient for 1B1-2 and 18A4-B8.
 origin: Recombinant containing left end of In(1)y[4] and
  right end of In(1)sc[9].
 references: Norton and Valencia, 1965, DIS 40: 40.
 genetics: Deficient for ac, sby, smd, and coc but not
  l(1)J1, fu, hdp, bkl, obl, crk, ton, bk, thl, or
  pph. Either deficient for y or carries
  y[4]. Male lethal.
#
In(1)y[5]
 cytology: In(1)1A-B;14D x ller and Raffel).
 discoverer: Patterson.
 genetics: Mutant for y. Recessive lethal associated with
  right breakpoint.
#
In(1)y[G]: Inversion (1) yellow of Goldschmidt
 cytology: In(1)1A;1C3-4 (Kodani).
 origin: Spontaneous.
 discoverer: Goldschmidt.
 synonym: In(1)y[px bl].
 genetics: Mutant for y.
#
In(1)z2: Inversion (1) zeste
 cytology: Dp(1;1)2C10-D1;4D2-4;18F-19A.
 new order:: 1 - 4D2|18F - 2D1|19A - 20.
 origin: X ray induced.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg.,
  Suppl. 38: 1-90.
#
In(1LR)l-v139: Inversion (1LR) lethal-variegated
 cytology: In(1LR)3C6-7.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
  Gersh, 1965, Genetics 51: 477-80 (fig.).
 genetics: Variegated for w, rst, and a lethal; requires two
  Y chromosomes for survival; X/Y/Y male
  fertile. Recombinant carrying left end of the
  4[D]X[P] element of T(1;4)w[m5] =
  T(1;4)3C3-4;101F1-2 and right end of
  In(1LR)l-v139 variegates for w but not for
  rst or the lethal.
#
In(1LR)sc[260-25]: Inversion (1LR) scute
 cytology: In(1LR)1B2-3.
 origin: X ray induced.
 discoverer: Sutton, 39k.
 synonym: Tp(1)sc[260-25].
 references: 1940, Genetics 25: 628-35 (fig.).
 genetics: Mutant for sc; variegates for y and ac
  but not svr. Genetic tests indicate loci of
  l(1)J1, y, and ac are located at the base of
  X to the right of bb. Sutton judged it to
  be a transposition of 1A1-B2 into the proximal
  heterochromatin, but since this requires three
  breaks with one to the left of 1A1, a pericentric
  inversion is deemed more probable. Recombination
  between In(1LR)sc[260-25] and a normal sequence
  yields Df(1)sc[260-25] = Df(1)1B2-3 and
  Dp(1;1)sc[260-25] = Dp(1;1)1B2-3. The
  deficiency is deficient for l(1)J1, y, and ac
  (Sutton, 1940).
#
In(1LR)sc[V1] Inversion (1LR) scute of Valencia
 cytology: In(1LR)1A8-C3; inferred from genetic results.
 origin: Gamma ray induced.
 discoverer: J. I. Valencia, 46h23.
 synonym: Inp(1)sc[V1] (Inp symbolizes a pericentric
  inversion).
 references: Muller and Valencia, 1947, DIS 21: 69-70.
 genetics: Mutant for ac and sc. A single exchange
  between In(1LR)sc[V1] and a normal X
  chromosome produces one recombinant with the left
  end of In(1LR)sc[V1] that is deficient for the
  tip of X, Df(1)sc[V1], and one with the right end
  of In(1LR)sc[V1] that is duplicated for the tip
  of X, Dp(1;1)sc[V1]. Left break
  between ac and M(1)Bld based on observation
  that Dp(1;1)sc[V1] is duplicated for ac, and
  Df(1)sc[V1] is deficient for ac but not
  M(1)Bld. Right break in XR. Dp(1;1)sc[V1]
  carrying y in normal position and y[+] in
  duplicated region provides an excellent marker system
  for right end of the X.
#
In(2)bw[R18]: Inversion (2) brown-Rearranged
 cytology: In(2)40F-41A;59E4-F1.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R18].
#
In(2)bw[R35]
 cytology: In(2)40F-41A;59D11-E1.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R35].
#
In(2)bw[R45]
 cytology: In(2)40F-41A;59E3-4.
 origin: X-ray-induced derivative of bw.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R45].
#
In(2)bw[R47]
 cytology: In(2)40-41;59D11-E1.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R47].
#
In(2)bw[R56]
 cytology: In(2)40F-41A;59D-E.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R56].
#
In(2)bw[R67]
 cytology: In(2)40F-41A;59E4-F1.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R67].
#
In(2)bw[R73]
 cytology: In(2)40-41A;59E4-F1.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R73].
#
In(2)bw[R79]
 cytology: In(2)40F-41A;59F2-3.
 origin: X ray induced.
 discoverer: Slatis, 50g26.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R79].
#
In(2)C56: Inversion (2) Crossover suppressor
 cytology: In(2)40-41;59B; position of left breakpoint in
  relation to centromere not determined.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination between b and
  sp strongly reduced.
#
In(2)C113
 cytology: In(2)40-41;46D; position of left break with
  respect to centromere not determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between b and
  sp reduced.
#
In(2)C162
 cytology: In(2)36B-C;40-41; position of right breakpoint
  with respect to centromere not determined. May
  contain a T(2;3).
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination between al and
  b reduced rather sharply.
#
In(2)C224
 cytology: In(2)25E;40-41; position of right breakpoint
  with respect to centromere not determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between al and
  b virtually eliminated.
#
In(1)C282
 cytology: In(2)31E;40-41; position of right breakpoint
  with respect to centromere not determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination between al and
  b strongly reduced.
#
In(2L)53d
 cytology: In(2L)25A;29F.
 origin: Neutron induced.
 discoverer: Mickey, 53d4.
 references: 1963, DIS 38: 29.
 genetics: Eye color mottled.
#
In(2L)A
 cytology: In(2L)26A;33E.
 origin: Naturally occurring inversion.
 discoverer: Oshima and Watanabe.
 references: 1965, DIS 40: 88.
#
In(2L)ast[rv2]: Inversion (2L) asteroid-reverted
 cytology: In(2L)21E2-3;31.
 origin: X ray induced in ast.
 discoverer: E. B. Lewis, 1942.
 references: 1945, Genetics 30: 158.
 genetics: Partial reversion of ast.
#
In(2L)C123 Inversion (2L) Crossover suppressor
 cytology: In(2L)23D-E;38C;39A.
 new order:: 21 - 23D|39A - 38C|23E - 38C|39A
  - 60.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination reduced in 2L.
#
In(2L)C127
 cytology: In(2L)23C;32A.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination between al and
  b virtually eliminated.
#
In(2L)C236.
 cytology: In(2L)22B;25F.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between al and
  b reduced.
#
In(2L)C263
 cytology: In(2L)24C;25F;26F; 25F-26F missing.
 new order:: 21 - 24C|25F - 24C|26F - 60.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: In(2L)C263/SM1 and In(2L)C263/SM5 females
  nearly sterile. Recombination reduced in 2L.
  Homozygous lethal.
#
In(2L)Cy: Inversion (2L) Curly
 cytology: In(2L)22D1-2;33F5-34A1.
 origin: Naturally occurring inversion.
 discoverer: Ward, 21f.
 references: 1923, Genetics 8: 276-300.
  Sturtevant, 1931, Carnegie Inst. Wash. Publ. No. 421: 20.
 genetics: Exists with and without Cy. Homozygous viable
  without Cy. Crossing over in In(2L)Cy/+
  heterozygote greatly reduced in 2L.
 genetics: The combination of In(2L)Cy + In(2R)Cy often used
  to balance chromosome 2. Balancers usually
  carry a dominant such as Cy, S[2], Bl, or
  L[4] and one or more of the following: al[2],
  dp[lv2], dp[lvI], E(S), b, pr, lt[3], cn[2],
  bw[45a], sp[2], or[45a].
#
In(2L)Cy[L]t[R]: Inversion (2L) Curly-Left t-Right
 cytology: In(2L)22D1-2;33F5-34A1[L]22D3-E1;34A8-9[R].
  Deficient for 22D2 and 34A1-8.
 origin: Recombinant carrying left end of In(2L)Cy and
  right end of In(2L)t.
 discoverer: Bridges.
 references: Morgan, Bridges, and Schultz, 1937, Carnegie
  Inst. Wash. Year Book 36: 300-1.
 genetics: Acts as suppressor of S; usually carries Cy.
#
In(2L)dp[olvR] Inversion (2L) dumpy-oblique lethal vortex Ruffled
 cytology: In(2L)25A;25B3-4.
 origin: X ray induced.
 discoverer: Schultz, 33a25.
 genetics: Mutant at dp. Homozygous lethal.
#
In(2L)ho[40]: Inversion (2L) heldout
 cytology: In(2L)21D4-E1;22E2-3.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 synonym: In(2L)ho.
 references: 1945, Genetics 30: 137-66.
 genetics: Mutant for ho but not S or ast.
  Homozygous male sterile.
#
In(2L)K
 cytology: In(2L)22D;26B.
 discoverer: Oshima and Watanabe.
 references: 1965, DIS 40: 88.
#
In(2L)lt[m2]: Inversion (2L) light-mottled
 cytology: In(2L)22F-23A;40B-F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2L)lt[m20]
 cytology: In(2L)32C;40B-F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2L)lt[m26]
 cytology: In(2L)27C;40B-F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2L)M1: Inversion (2L) of Mourad
 cytology: In(2L)38E;40F.
 origin: Spontaneous.
 discoverer: Mourad and Mallah.
 references: 1960, Evolution 14: 166-70.
#
In(2L)M2
 cytology: In(2L)21F;33A.
 origin: Spontaneous.
 discoverer: Mourad and Mallah.
 references: 1960, Evolution 14: 166-70.
#
In(2L)NS: Inversion (2L) from Nova Scotia
 cytology: In(2L)23E2-3;35F1-2 |idges and Li in Morgan,
  Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 292).
 origin: Naturally occurring inversion.
 discoverer: Sturtevant, 13i.
 synonym: CIIL; C2L.
 references: Sturtevant, 1919, Carnegie
  Inst. Wash. Publ. No. 278: 305-41.
 genetics: Crossing over in 2L greatly reduced; none
  between S and b; 0.3% between b and
  pr.
#
In(2L)t: Inversion (2L) t
 cytology: In(2L)22D3-E1;34A8-9 |idges and Li in Morgan,
  Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 292).
 origin: Naturally occurring inversion.
 discoverer: Bridges, 21a30.
 synonym: C(2;3); C(2L)T; C(2L)HR.
 references: Sturtevant, 1931, Carnegie Inst. Wash. Publ. No. 421: 20.
 genetics: Found in many natural populations (e.g., Warters,
  1944, Texas Univ. Publ. 4445: 129-74; Oshima and
  Watanabe, 1965, DIS 40: 88).
#
In(2L)Tg: Inversion (2L) Tegula
 cytology: In(2L)21C;22F.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1962.
 references: Mora, 1963, DIS 38: 32.
 genetics: Associated with Tg.
#
In(2LR)40d
 cytology: In(2LR)26D;41A-B.
 origin: X ray induced.
 discoverer: T. Hinton and Atwood, 49d.
 references: Demerec, Kaufmann, Sutton, and Fano, 1941, Carnegie
  Inst. Wash. Year Book 40: 225-34.
  Hinton, 1942, DIS 16: 48.
 genetics: Variegated for a dominant dark eye color and
  irregular facets; more extreme at low temperature.
  Homozygous lethal. Certain stocks containing
  In(2LR)40d fail to grow on media lacking RNA or
  adenine (Hinton, Ellis, and Noyes, 1951,
  Proc. Natl. Acad. Sci. U.S. 37: 293-99). This was true at pH 7.0
  but not at pH 5.0 (Ellis, 1959, Physiol. Zool. 32: 29-39).
#
In(2LR)102
 cytology: In(2LR)26A;51C + In(2R)41;57A.
 new order:: 21 - 26A|51C - 41|57A - 51C|26A
  - 41|57A - 60.
 origin: X ray induced in ds[W] sp[2].
 discoverer: R. F. Grell, 53k.
 references: Kramer and Lewis, 1956, J. Heredity 47: 132-36.
  Grell and Lewis, 1956, DIS 30: 71.
 genetics: Useful as a balancer.
#
In(2LR)a[M60]: Inversion (2LR) arc of Meyer
 cytology: Breakpoints unknown.
 origin: X ray induced.
 discoverer: Meyer, 60f.
 references: 1963, DIS 37: 50.
 genetics: Associated with a[M60].
#
In(2LR)al[M60] Inversion (2LR) aristaless of Meyer
 origin: X ray induced.
 discoverer: Meyer, 60f.
 references: 1963, DIS 37: 50.
 genetics: Mutant for al. Homozygous lethal. Inversion
  inferred fron crossing over inhibition in 2L and
  2R.
#
In(2LR)al[v] Inversion (2LR) aristaless-variegated
 cytology: In(2LR)21B-C1;41.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 137-66.
 genetics: Variegated for al. Homozygous lethal.
#
In(2LR)bw[R3]: Inversion (2LR) brown-Rearranged
 cytology: In(2LR)40F;51F;55E;57E;58D8-9.
 new order:: 21 - 40F|55E - 51F|57E - 55E|57E
  - 59D8|51F - 40F|59D9 - 60.
 origin: X-ray-induced derivative of bw.
 discoverer: Slatis, 48k16.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R3].
#
In(2LR)bw[R20]
 cytology: In(2LR)40D;59D5-6.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R20].
#
In(2LR)bw[R55]
 cytology: In(2LR)24E1-D;42E + In(2R)40F-41A;59D4-5.
 new order:: 21 - 24D|42E - 41A|59D4 - 42E|24E1
  - 40F|59D5 - 60.
 origin: X ray induced.
 discoverer: Slatis, 50d23.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R55].
#
In(2LR)bw[V1]: Inversion (2LR) brown-Variegated
 cytology: In(2LR)21C8-D1;60D1-2 + In(2LR)40F;59D4-E1.
 new order:: 21A - 21C8|60D1 - 59E1|40F -
  59D4|40F - 21D1|60D2 - 60F.
 origin: X ray induced.
 discoverer: Muller, 1929.
 synonym: Ins(2LR)Pm: Inversion (2LR) Plum.
 references: 1930, J. Genet. 22: 299-334 (fig.).
  Glass, 1934, J. Genet. 28: 69-112 (fig.).
  1934, Am. Naturalist 68: 107-14.
  Bridges, 1937, Cytologia (Tokyo), Fujii
  Jub., Vol. 2: 745-55.
 genetics: Mutant for ds; variegated for lt, bw, mi,
  and abb. al[4] arose after origin. Double
  crossovers in 2L but not 2R fairly frequent.
  Single exchange in region 21D1-40F of 2L between
  In(2LR)bw[V1] and a normal sequence produces a
  recombinant carrying left end of normal chromosome 2,
  which is duplicated for 21A1-C8 and deficient
  for 60D2-F5. Heterozygote for this recombinant
  poorly viable, fertile, brown-Variegated, Minute,
  and dwarf with pebbled arc wings; deficient for
  locus of M(2)c. Reciprocal recombinant
  deficient for 21A1-C8 and duplicated for 60D2-F5;
  heterozygote poorly viable, fertile, bw[+],
  Minute giant; deficient for al and M(2)21C1-2.
#
In(2LR)bw[V29l]
 origin: X ray induced.
 discoverer: Van Atta.
 references: 1932, Genetics 17: 637-59.
 genetics: Variegated for bw. Breaks most probably just to
  the left of centromere and near bw.
#
In(2LR)bw[V30k1]
 origin: X ray induced.
 discoverer: Van Atta.
 references: 1932, Genetics 17: 637-59.
 genetics: Variegated for bw. Breaks most likely just to
  the left of centromere and near bw.
#
In(2LR)bw[V32g]
 cytology: In(2LR)40F;59E.
 origin: X ray induced.
 discoverer: Dobzhansky, 32g6.
 synonym: In(2LR)Pm[2]: Inversion (2LR) Plum-2.
 references: Schultz and Dobzhansky, 1934, Genetics 19: 344-64.
  Schultz, 1936, Proc. Natl. Acad. Sci. U.S. 22: 27-33.
 genetics: Variegated for bw.
#
In(2LR)C251 Inversion (2LR) Crossover suppressor
 cytology: In(2LR)36F;57B.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination reduced in 2R.
#
In(2LR)D
 cytology: In(2LR)36F;49B.
 discoverer: Oshima and Watanabe.
 references: 1965, DIS 40: 88.
#
In(2LR)Gla: Inversion (2LR) Glazed
 cytology: In(2LR)27D;51E superimposed on
  In(2L)22D1-E1;33F4-34A9 (Morgan, Bridges, and
  Schultz, 1936, Carnegie Inst. Wash. Year Book 35: 293;
  Grell and Grell, 1962, DIS 36: 71).
 new order:: 21 - 22D1|33F5 - 27D|51E -
  34A9|22E1 - 27D|51E - 60.
 origin: X ray induced in chromosome containing In(2L)Cy =
  In(2L)22D1-2;33F5-34A1 or In(2L)t =
  In(2L)22D3-E1;34A8-9.
 genetics: Associated with Gla. Effective crossover
  suppressor; no single or double crossovers recovered
  to the left of c (Alexander, 1952, Texas
  Univ. Publ. 5204: 219-26).
#
In(2LR)lt[m3]: Inversion (2LR) light-mottled
 cytology: In(2LR)40B-F;60D.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2LR)lt[m9]
 cytology: In(2LR)40B-F;56E.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2LR)lt[m12]
 cytology: In(2LR)40B-F;60D.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2LR)lt[m22]
 cytology: In(2LR)40B-F;59D.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2LR)lt[m25]
 cytology: In(2LR)40B-F;57C-D.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2LR)lt[m33]
 cytology: In(2LR)40B-F;58E.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
In(2LR)O: Inversion (2LR) of Oster
 cytology: In(2LR)30E-F;50C10-D1 superimposed on
  In(2L)22D1-2;33F5-34A1 + In(2R)42A2-3;58A4-B1
  (Lindsley).
 new order:: 20 - 22D1|33F5 - 30F|50D1 -
  58A4|42A2 - 34A1|22D2 - 30E|50C10
  - 42A3|58B1 - 60.
 origin: X ray induced in In(2L)Cy + In(2R)Cy, Cy dp[lvI]
  pr cn[2].
 discoverer: Oster.
 references: 1956, DIS 30: 145.
 genetics: Used as a balancer for chromosome 2, described
  as CyO in the section on balancers.
#
In(2LR)px[52g]: Inversion (2LR) plexus
 origin: X ray induced in cn crs.
 discoverer: Iyengar and Meyer, 52g.
 references: 1956, DIS 30: 73.
  Meyer, 1956, DIS 30: 81.
  1958, DIS 32: 83.
 genetics: Mutant for px. Pericentric inversion with
  breakpoints between dp and b and between
  px and sp. Homozygous female fertile but
  male sterile. Male genitalia rotated. Sterility
  factor not allelic to ab and not covered by
  duplication in bw[+]Y, as is crs, the male
  sterility factor present in original chromosome.
#
In(2LR)Px[4]: Inversion (2LR) Plexate
 cytology: In(2LR)22A3-B1;60B-C[L];21C8-D1;60D1-2[R] +
  In(2R)42A2-3;58A4-B1; deficient for 60B-D1 and
  duplicated for 21D1-22A3.
 new order:: 21A - 22A3|60B - 58B1|42A3 -
  58A4|42A2 - 21D1|60D2 - 60F.
 origin: Synthetic. This chromosome is a recurrent product
  of recombination in region 33F-40F between
  In(2LR)21C8-D1;60D1-2 from In(2LR)bw[V1]
  [In(2LR)21C8-D1;60D1-2 + In(2LR)40F;59D4-E1] and
  In(2LR)22A3-B1;60B-C from SM1 [In(2L)Cy =
  In(2L)22D1-2;33F5-34A1 + In(2LR)22A3-B1;60B-C +
  In(2R)Cy = In(2R)42A2-3;58A4-B1]. Recombinant
  carries tip of 2L and In(2R)Cy from SM1
  and tip of 2R and most of 2L from
  In(2LR)bw[V1]. The reciprocal recombinant is
  In(2LR)S[56f].
 discoverer: Thompson.
 references: Burdick, 1956, DIS 30: 69.
 genetics: Deficient for bs, ba, Pin, Px, and probably
  sp; duplicated for S.
#
In(2LR)Rev: Inversion (2LR) Revolute
 cytology: In(2LR)40F;52D10-E1 |idges and Li in Morgan,
  Bridges, and Schultz, 1936, Carnegie Inst. Wash. Year
  Book 35: 293).
 origin: X ray induced.
 discoverer: Dobzhansky, 31b5.
 genetics: Variegated for lt and Rev.
#
In(2LR)Rev[B] Inversion (2LR) Revolute of Bridges
 cytology: In(2LR)40;52C-E (E. B. Lewis).
 origin: Spontaneous.
 discoverer: Bridges, 36e22.
 synonym: In(2LR)Rvd.
 references: Morgan, Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 293.
 genetics: Mutant or variegated for Rev.
#
In(2LR)S[56f]: Inversion (2LR) Star
 cytology: In(2L)22D1-2;33F5-34A1 +
  In(2LR)21C8-D1;60D1-2[L]22A3-B1;60B-C[R] +
  In(2LR)40F;59D4-E1; deficient for 21D1-22A3 and
  duplicated for 60B-D1.
 new order:: 21A - 21C8|60D1 - 50E1|40F -
  59D4|40F - 34A1|22D1 - 33F5|22D1 -
  22B1|60C - 60F.
 origin: Synthetic. This chromosome is a recurrent product of
  recombination in region 33F-40F between
  In(2LR)21C8-D1;60D1-2 from In(2LR)bw[V1]
  [In(2LR)21C8-D1;60D1-2 + In(2LR)40F;59D4-E1] and
  In(2LR)22A3-B1;60B-C from SM1 [In(2L)Cy =
  In(2L)22D1-2;33F5-34A1 + In(2LR)22A3-B1;60B-C +
  In(2R)Cy = In(2R)42A2-3;58A4-B1]. Recombinant
  carries the tip of 2L and In(2LR)40F;59D4-E1
  from In(2LR)bw[V1] and the tip of 2R and
  In(2L)Cy from SM1. Reciprocal recombinant
  is In(2LR)Px[4].
 discoverer: Thompson.
 references: Burdick, 1956, DIS 30: 69.
 genetics: Deficient for S; duplicated for Px.
#
In(2LR)S[325]
 cytology: In(2LR)21D2-3;21D3-E2;21E2-3;41.
 new order:: 21A - 21E2|41 - 21D3|41 - 60.
  Tentative.
 origin: X ray induced in Dp(2;2)S = Dp(2;2)21D2-3;21E2-3.
 discoverer: E. B. Lewis.
 genetics: Break in 2L either in or between duplicated
  segments of Dp(2;2)S.
#
In(2LR)S[K]: Inversion (2LR) Star of Krivshenko
 cytology: Breakpoints near ends of 2L and 2R.
 discoverer: Krivshenko.
 references: 1936, DIS 5: 8.
 genetics: Associated with S[K].
#
In(2LR)SM1: Inversion (2LR) Second Multiple
 cytology: In(2LR)22A3-B1;60B-C superimposed on
  In(2L)22D1-2;33F5-34A1 + In(2R)42A2-3;58A4-B1.
 new order:: 21 - 22A3|60B - 58B1|42A3 -
  58A4|42A2 - 34A1|22D2 - 33F5|22D1
  - 22B1|60C - 60F.
 origin: X ray induced in In(2L)Cy + In(2R)Cy.
 discoverer: R. F. Grell, 1953.
 references: 1953, DIS 27: 58.
 genetics: The pericentric inversion, In(2LR)22A3-B1;60B-C,
  enhances balancing power of In(2L)Cy + In(2R)Cy
  since it causes the single crossover between the two
  Cy inversions to yield complementary products
  that are dominant lethal.
 genetics: Used as a balancer for chromosome 2, described
  as SM1 in the section on balancers.
#
In(2LR)SM5
 cytology: In(2L)21D2-3;36C + In(2L)29C-E;40F +
  In(2R)42D;53C;58F superimposed on
  In(2L)22D1-2;33F5-34A1 + In(2LR)22A3-B1;60B-C +
  In(2R)42A2-3;58A4-B1. Duplicated for regions
  42A3-D and 58B1-F.
 new order:: 21A - 21D2|36C - 40F|29C -
  22D2|34A1 - 36C|21D3 - 22A3|60B -
  58B1|42A3 - 42D|42D - 42A3|58B1 -
  58F|53C - 42D|53C - 58A4|42A2 -
  40F|29E - 33F5|22D1 - 22B1|60C -
  60F.
 origin: X ray induced in several steps in In(2LR)SM1.
 discoverer: R. F. Grell, 1955.
 references: Mislove and Lewis, 1955, DIS 29: 75.
 genetics: Variegated for lt owing to In(2L)29C-E;40F.
  In(2LR)SM5/M(2)1 lethal (C. Hinton); probably
  related to break in 58F.
 genetics: Excellent balancer for all of chromosome 2,
  described as SM5 in the section on balancers.
#
In(2LR)U: Inversion (2LR) Upturned
 origin: X ray induced.
 discoverer: Ball, 32a27.
 references: 1935, DIS 3: 17.
 genetics: Associated with U.
#
In(2R)41-47
 cytology: In(2R)41A;47A.
 origin: X ray induced simultaneously with T(1;2)B[bd].
 discoverer: Bridges.
 references: Morgan, Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 291.
 genetics: Probably not separable from T(1;2)B[bd] =
  T(1;2)16A1-2;48C2-3.
#
In(2R)bw[A]: Inversion (2R) brown-Auburn
 cytology: In(2R)41;59D.
 origin: X ray induced.
 discoverer: Dubinin.
 synonym: In(2R)Pm[D1].
 references: 1936, Biol. Zh. (Moscow) 5: 851-66.
 genetics: Variegated for bw and mi; variegation for
  bw dominant to bw. Dubinin claims
  brown-Variegated effect exists at both ends of the
  inversion.
 genetics: Ninety-one secondary rearrangements derived from
  irradiation of In(2R)bw[A] analyzed by Dubinin.
#
In(2R)bw[AL]Cy[R] Inversion (2R) brown-Auburn Left Curly-Right
 cytology: In(2R)41;59D[L]42A2-3;58A4-B1[R]; deficient
  for 41-42A2 and duplicated for 58B1-59D.
 origin: Recombinant carrying left end of In(2R)bw[A] and
  right end of In(2R)Cy.
 references: Dubinin, 1936, Biol. Zh. (Moscow) 5: 851-66.
 genetics: Variegated for bw; Minute, presumably owing to
  deficiency for M(2)S2. Wings divergent with
  incised inner margins.
#
In(2R)bw[R32]: Inversion (2R) brown-Rearranged
 cytology: In(2R)41A;59D.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R32].
#
In(2R)bw[R33]
 cytology: In(2R)41;59D-E.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R33].
#
In(2R)bw[V2]: Inversion (2R) brown-Variegated
 origin: X ray induced.
 discoverer: Harris, 1929.
 references: Muller, 1930, J. Genet. 22: 299-34.
  Glass, 1933, J. Genet. 28: 69-112.
  1934, Am. Naturalist 68: 107-14.
 genetics: Variegated for bw. Linkage data indicate that
  one break is just to the right of centromere.
#
In(2R)bw[V7]
 origin: X ray induced.
 discoverer: Winchester, 1932.
 references: 1938, DIS 9: 23.
  Glass, 1939, DIS 12: 47.
 genetics: Variegated for bw. One break at bw and
  another to the right of spindle attachment of 2R.
  Gives viable recombinants with In(2R)Cy =
  In(2R)42A2-3;58A4-B1.
#
In(2R)bw[V30k10]
 origin: X ray induced.
 discoverer: Van Atta, 30k10.
 references: 1932, Genetics 17: 637-59.
 genetics: Variegated for bw.
#
In(2R)bw[V34k]
 cytology: In(2R)41;59E superimposed on
  In(2R)42A2-3;58A4-B1.
 new order:: 21 - 41|59E - 58B1|42A3 - 58A4|42A2
  - 41|59E - 60.
 origin: X ray induced in In(2R)Cy.
 discoverer: Oliver, 34k22.
 references: 1937, DIS 7: 19.
 genetics: Variegated for bw. Recombination in region
  43A3-58A4 between In(2R)bw[V34k]+Cy and a
  normal sequence produces reciprocal
  duplication-deficiency types: Df(2R)bw[V34kL]Cy[L]
  + Dp(2R)Cy[R]bw[V34kR] = Df(2R)41;42A2-3 +
  Dp(2R)58A4-B1;59 (i.e., 21 - 41|59E -
  58B1|42A3 - 60) and Dp(2R)bw[V34kL]Cy[L] +
  Df(2R)Cy[R]bw[V34kR] = Dp(2R)41;42A2-3 +
  Df(2R)58A4-B1;59 (i.e., 21 - 58A4|42A2 -
  41|59 - 60).
#
In(2R)bw[V40b]
 cytology: In(2R)41A-B;59D-E.
 origin: X ray induced.
 discoverer: T. Hinton, 40b.
 references: Atwood, 1942, DIS 16: 47.
 genetics: Variegated for bw.
#
In(2R)bw[V54a]
 cytology: In(2R)41A-B;59D4-9.
 origin: Gamma ray induced.
 discoverer: Mickey, 54a6.
 references: 1963, DIS 38: 29.
 genetics: Variegated for bw.
#
In(2R)bw[V54b]
 cytology: In(2R)41A;60D9-11 (seems unlikely that right
  break at 60D9-11, perhaps at 59D9-11).
 origin: Neutron induced.
 discoverer: Mickey, 54b12.
 references: 1963, DIS 38: 29.
 genetics: Variegated for bw.
#
In(2R)bw[V54c]
 cytology: In(2R)41;59E1.
 origin: Neutron induced.
 discoverer: Yanders, 54c5.
 references: Mickey, 1963, DIS 38: 29.
 genetics: Variegated for bw.
#
In(2R)bw[VDe1] Inversion (2R) brown-Variegated of Demerec
 cytology: In(2R)41B2-C1;59E2-4 [Bridges, 1937, Cytologia
  (Tokyo), Fujii Jub., Vol. 2: 745-55].
 origin: X ray induced.
 discoverer: Demerec, 33i28.
 genetics: Variegated for bw.
#
In(2R)bw[VDe1L]Cy[R] Inversion (2R) brown- Variegated of Demerec 1 Left Curly-Right
 cytology: In(2R)41B2-C1;59E2-4[L]42A2-3;58A4-B1[R];
  deficient for 41C1-42A2 and duplicated for
  58B1-59E2.
 origin: Recombinant carrying left end of In(2R)bw[VDe1]
  and right end of In(2R)Cy.
 genetics: Deficient for M(2)S2 but not rl or
  M(2)p; duplicated for M(2)l, bw, and mi.
#
In(2R)bw[VDe2]
 cytology: In(2R)41A-B;59D6-E1 [Bridges, 1937, Cytologia
  (Tokyo), Fujii Jub., Vol. 2: 745-55].
 origin: X ray induced.
 discoverer: Demerec, 33j14.
 genetics: Variegated for bw. Left break to the right of
  rl and right break between bw and mi.
#
In(2R)bw[VDe2L]Cy[R] Inversion (2R) brown- Variegated of Demerec 2 Left Curly-Right
 cytology: In(2R)41A-B;59D6-E1[L]42A2-3;58A4-B1[R];
  deficient for 41B-42A2 and duplicated for 58B1-59D6.
 origin: Recombinant carrying left end of In(2R)bw[VDe2]
  and right end of In(2R)Cy.
 genetics: Duplicated for M(2)l and bw but not
  mi; deficient for M(2)S2 but not rl or
  M(2)p.
#
In(2R)bw[VI] Inversion (2R) brown-Variegated of Ives
 cytology: In(2R)41A;59D.
 origin: Spontaneous.
 discoverer: Ives, 38l13.
 references: 1950, DIS 24: 58.
 genetics: Associated with bw[VI].
#
In(2R)C72: Inversion (2R) Crossover suppressor
 cytology: In(2R)50E;57F;60D.
 new order:: 21 - 50E|57F - 60D|57F - 50E|60D
  - 60F.
 origin: X ray induced.
 discoverer: Roberts and D. Stewart, 1964.
 genetics: Homozygous viable. Recombination between b and
  sp sharply reduced.
#
In(2R)C129
 cytology: In(2R)43F;56E.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between b and
  sp reduced.
#
In(2R)Cy: Inversion (2R) Curly
 cytology: In(2R)42A2-3;58A4-B1 |idges and Li in Morgan,
  Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 292).
 origin: Spontaneous.
 discoverer: L. Ward, 21f.
 references: 1923, Genetics 8: 276-300.
  Sturtevant, 1931, Carnegie Inst. Wash. Publ. No. 421: 20.
  Graubard, 1932, Genetics 17: 81-105.
 genetics: Left breakpoint between ap and pk. Homozygous
  viable and fertile. Crossing over in 2R
  strongly reduced. Carries cn[2] in most
  laboratory stocks.
 genetics: Used in combination with In(2L)Cy as a balancer
  for chromosome 2.
#
In(2R)Cy[L]bw[VDe1R] Inversion (2R) Curly-Left brown-Variegated of Demerec 1 Right
 cytology: In(2R)42A2-3;58A4-B1[L]41B2-C1;59E2-4[R];
  duplicated for 41C1-42A2 and deficient for
  58B1-59E2.
 origin: Recombinant carrying left end of In(2R)Cy and
  right end of In(2R)bw[VDe1].
 genetics: Deficient for M(2)l, bw, and mi; duplicated
  for M(2)S2 but not rl or M(2)p.
#
In(2R)Cy[L]bw[VDe2R] Inversion (2R) Curly-Left brown-Variegated of Demerec 2 Right
 cytology: In(2R)42A2-3;58A4-B1[L]41A-B;59D6-E1[R];
  duplicated for 41B-42A2 and deficient for 58B1-59D6.
 origin: Recombinant carrying left end of In(2R)Cy and
  right end of In(2R)bw[VDe2].
 genetics: Deficient for M(2)l and bw but not mi;
  duplicated for M(2)S2 but not rl or M(2)p.
#
In(2R)G: Inversion (2R) Gallup
 cytology: In(2R)50E;54D (T. Hinton).
 origin: Spontaneous.
 discoverer: Ives.
 references: 1957, DIS 31: 83.
 genetics: Associated with N-2G. Crossing over in 2R
  reduced to about 13%.
#
In(2R)M: Inversion (2R) of Mourad
 cytology: In(2R)54F1-55A1;58F-59A.
 origin: Spontaneous.
 discoverer: Mourad and Mallah.
 references: 1960, Evolution 14: 166-70.
#
In(2R)NS: Inversion (2R) from Nova Scotia
 cytology: In(2R)52A2-B1;56F9-13 |idges and Li in
  Morgan, Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 292-3).
 origin: Naturally occurring inversion.
 discoverer: Sturtevant, 13i.
 synonym: C(2)R.
 references: Sturtevant, 1919, Carnegie Inst. Wash. Publ. No. 278: 305-41.
  1931, Carnegie Inst. Wash. Publ. No. 421: 1-27.
 genetics: Crossing over reduced to about 1.5% between
  centromere and inversion and to about 0.1% between
  inversion and tip of chromosome.
 genetics: Found in many natural populations (e.g., Warters,
  1944, Texas Univ. Publ. 4445: 129-74; Oshima and
  Watanabe, 1965, DIS 40: 88).
#
In(2R)Pu[K]: Inversion (2R) Punch of Krivshenko
 cytology: In(2R)41;57E-F.
 origin: X ray induced.
 discoverer: Krivshenko, 53k24.
 synonym: In(2R)Pm[K].
 references: 1954, DIS 28: 75.
 genetics: Associated with Pu[K] (Rowan). Pu[K]/Pu[2]
  is lethal.
#
In(2R)vg[U]: Inversion (2R) vestigial-Ultra
 cytology: In(2R)49C1-2;50C1-2 (Ratty and Lindsley, 1964,
  DIS 38: 30).
 origin: Gamma ray induced.
 discoverer: Ives, 55l31.
 references: 1956, DIS 30: 72-73.
 genetics: Associated with vg[U]. Homozygous lethal.
#
In(3)C41: Inversion (3) Crossover suppressor
 cytology: In(3)80-81;91E-F; position of left breakpoint
  with respect to centromere not determined.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination between st and
  ca reduced.
#
In(3)C229
 cytology: In(3)67B;80-81; position of right breakpoint
  with respect to centromere not determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between ve and
  st sharply reduced.
#
In(3)C289
 cytology: In(3)80-81;93E; position of left breakpoint
  with respect to centromere not determined. May also
  contain a T(2;3).
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between st and
  ca reduced.
#
In(3)p[100.48]: Inversion (3) pink
 cytology: In(3)80-81;85A6-B1; position of left
  breakpoint with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for p.
#
In(3)p[100.88]
 cytology: In(3)80-81;94D11-E1; position of left
  breakpoint with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for p.
#
In(3L)100.307
 cytology: In(3L)62E2-4;64C2-4.
 origin: X ray induced simultaneously with e[100.307].
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
#
In(3L)100r2
 cytology: In(3L)76A4-B1;80 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 61 - 76A4|(3C1 - 4B4)|80 - 76B1|80
  - 100.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh, 1959.
 synonym: N[264-100]r[2].
 references: 1959, Genetics 44: 163-72.
 genetics: Selected because white variegation darker than
  Dp(1;3)N[264-100]. Removes duplication from
  centromere region.
#
In(3L)100r8
 cytology: In(3L)73F1-74A1;80 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 61 - 73F1|(3C1 - 4B4)| 80 - 74A1 |
  80 - 100.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh, 1959.
 genetics: Selected as a partial reversion of white mottling in
  Dp(1;3)N[264-100]. Removes duplication from
  centromere region.
#
In(3L)100r11
 cytology: In(3L)65A1-B1;80 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 61 - 65A1|(3C1 - 4B4)|80 - 65B1|80
  - 100.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh, 1959.
 references: 1959, Genetics 44: 163-72.
 genetics: Selected as a partial reversion from white-mottled.
  Removes duplication from centromere region.
#
In(3L)Apt: Inversion (3L) Apart
 cytology: Breakpoints unknown.
 origin: X ray induced.
 discoverer: Belgovsky, 34e23.
 references: 1935, DIS 3: 27.
 genetics: Associated with Apt.
#
In(3L)Bit: Inversion (3L) Bitten
 cytology: Breakpoints unknown.
 origin: X ray induced.
 discoverer: Lefevre, 48g5.
 references: 1949, DIS 23: 58.
 genetics: Associated with Bit.
#
In(3L)C90: Inversion (3L) Crossover suppressor
 cytology: In(3L)62B;80C.
 origin: X ray induced.
 discoverer: Roberts and D. Stewart, 1964.
 genetics: Homozygous lethal. Recombination between ve and
  st sharply reduced.
#
In(3L)C299
 cytology: In(3L)63C;80.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between ve and
  st virtually eliminated.
#
In(3L)C302
 cytology: In(3L)63A;71A.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between ve and
  st virtually eliminated.
#
In(3L)D: Inversion (3L) Dichaete
 cytology: In(3L)69D3-E1;70C13-D1 |idges).
 origin: Spontaneous.
 discoverer: Bridges, 15a3.
 references: Morgan, Bridges, and Schultz, 1937, Carnegie
  Inst. Wash. Year Book 36: 301.
 genetics: Associated with D.
#
In(3L)h[100.12]: Inversion (3L) hairy
 cytology: In(3L)61A2-3;66D.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for h.
#
In(3L)h[100.239]
 cytology: In(3L)66D11-12;80C.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for h.
#
In(3L)M: Inversion (3L) of Mourad
 cytology: In(3L)66D;71D.
 origin: Spontaneous.
 discoverer: Mourad and Mallah.
 synonym: In(3L)F = In(3L)66C;71B of Oshima and Watanabe
  (1965, DIS 40: 88) probably the same.
 references: 1960, Evolution 14: 166-70.
#
In(3L)P: Inversion (3L) of Payne
 cytology: In(3L)63C;72E1-2 |idges and Li in Morgan,
  Bridges, and Schultz, 1937, Carnegie
  Inst. Wash. Year Book 36: 301).
 origin: Naturally occurring inversion.
 discoverer: Payne, 17g.
 references: 1918, Indiana Univ. Studies 5 No. 36: 1-45.
  1924, Genetics 9: 327-42.
  Sturtevant, 1931, Carnegie Inst. Wash. Publ. No. 421: 18.
 genetics: Homozygous viable, although it often contains
  lethals of independent origin.
 genetics: Often associated with In(3R)P. Much used as a
  balancer for 3L. Allows only about 0.02%
  crossing over between ru and st. Balancers
  contain recessive lethals or Me. Balancers for
  all of chromosome 3 made by combining
  In(3L)P with In(3R)P or In(3R)C. Found
  in many wild populations (e.g., Warters, 1944, Texas
  Univ. Publ. 4445: 129-174; Oshima and Watanabe,
  1965, DIS 40: 88).
#
In(3L)pers: Inversion (3L) persimmon
 cytology: In(3L)63C2-5;73B2-5.
 origin: X ray induced.
 discoverer: Demerec, 37l2.
 references: 1941, DIS 14: 40.
 genetics: Associated with pers.
#
In(3L)Spr: Inversion (3L) Spread
 cytology: Breakpoints unknown.
 origin: X ray induced.
 discoverer: Oliver, 32k21.
 references: 1935, DIS 4: 15.
 genetics: Associated with Spr.
#
In(3L)th[100.293]: Inversion (3L) thread
 cytology: In(3L)72A2-B1;76A4-B1;79A4-B1.
 new order:: 61 - 72A2|79A4 - 76B1|72B1 -
  76A4|79B1 - 100.
 origin: X ray induced.
 discoverer: Alexander.
 synonym: Tp(3)th[100.293].
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for th.
#
In(3LR)65;83
 origin: X ray induced simultaneously with, but subsequently
  separated from, T(2;3)Sb[V].
 discoverer: E. B. Lewis, 1948.
 references: 1956, DIS 30: 76-77.
#
In(3LR)100r1
 cytology: In(3LR)80;96B1-3 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 61 - 80|(3C1 - 4B4)|96B1 - 80|96B3
  - 100.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh.
 references: 1959, Genetics 44: 163-72.
 genetics: Selected as an almost complete reversion to wild
  type of the white-mottled effect of
  Dp(1;3)N[264-100]. Duplication removed from
  region of the centromere.
#
In(3LR)100r3
 cytology: In(3LR)80;86C1-D1 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 61 - 80|86C1 - 80|(3C1 - 4B4)|86D1
  - 100.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh.
 references: 1959, Genetics 44: 163-72.
 genetics: Does not remove duplication from region of
  centromere.
#
In(3LR)100r7
 cytology: In(3LR)80;99B-C1 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 61 - 80|99B - 80|(3C1 - 4B4)|99C1
  - 100.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh.
 references: 1959, Genetics 44: 163-72.
 genetics: Partial reversion of white-mottled to wild type.
  Duplication not removed from region of centromere.
#
In(3LR)100r27
 cytology: In(3LR)80;96B3-5 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 61 - 80|(3C1 - 4B4)|96B3 - 80|96B5
  - 100.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh.
 references: 1959, Genetics 44: 163-72.
 genetics: Almost complete reversion of the white-mottled to
  wild type. Break between duplication and
  centromere.
#
In(3LR)C35 Inversion (3LR) Crossover suppressor
 cytology: In(3LR)64B;89E.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination practically
  eliminated between ve and st and reduced
  between st and ca.
#
In(3LR)C117
 cytology: In(3LR)64D;89B.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination practically
  eliminated between ve and st.
#
In(3LR)C165
 cytology: In(3LR)64C;83C.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination between ve and
  st virtually eliminated.
#
In(3LR)C175
 cytology: In(3LR)65C;95E.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination practically
  eliminated between ve and st and between
  st and ca.
#
In(3LR)C190
 cytology: In(3LR)69F;89D.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced between
  ve and st and between st and ca.
#
In(3LR)C269
 cytology: In(3LR)78C;98F.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination between st and
  ca virtually eliminated.
#
In(3LR)C334
 cytology: In(3LR)67E;88D;91F.
 new order:: 61 - 67E|88D - 67E|91F - 88D|91F
  - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced between
  ve and st and between st and ca.
#
In(3LR)CxD Inversion (3LR) Crossover Suppressor Dichaete
 cytology: In(3LR)71F;85C + In(3LR)80;84A;93F superimposed
  on In(3L)69D3-E1;70C13-D1.
 new order:: 61A - 69D3|70C13 - 69E1|70D1 -
  71F|85C - 84A|80 - 84A|93F -
  85C|71F - 80|93F - 100 |idges).
 origin: X ray induced in In(3L)D.
 discoverer: Oliver.
 synonym: CxD; Dcx.
 references: Glass, 1933, J. Genet. 28: 70.
  Federova, 1937, Dokl. Acad. Nauk
  SSSR 14: 135-38.
 genetics: Carries D (separates from other inversions with
  frequency of 0.2%). Crossing over strongly reduced
  in chromosome 3 except distal half of 3L;
  virtually no crossing over between st and e.
 genetics: Name easily confused with what has been called
  C(3)x, which appears to be In(3L)P + In(3R)P
  (Lewis, 1956, DIS 30; 130).
#
In(3LR)DcxF Inversion (3LR) Dichaete crossover suppressor of Federova
 cytology: In(3L)62;67 superimposed on
  In(3L)69D3-E1;70C13-D1 + In(3LR)71F;85C +
  In(3LR)80;84A;93F. From Federova's drawings
  (1937), there appears to be an inversion from about
  62 to 67 in addition to a complex rearrangement,
  presumably In(3LR)CxD.
 new order:: 61 - 62|67 - 62|67 - 69D3|70C13
  - 69E1|70D1 - 71F|85C - 84A|80
  - 84A|93F - 85C|71F - 80|93F -
  100.
 origin: X ray induced in In(3LR)CxD.
 discoverer: Fedorova.
 synonym: In(3LR)CxF; DcxF; CxF,D.
 references: 1937, Dokl. Acad. Nauk SSSR 14: 135-38.
 genetics: Carries D. Crossing over strongly inhibited
  throughout chromosome 3.
#
In(3LR)Hi: Inversion (3LR) Hirsute
 cytology: In(3LR)71A;91F.
 origin: X ray induced.
 discoverer: Bishop, 1939.
 genetics: Associated with Hi.
#
In(3LR)K: Inversion (3LR) of Krivshenko
 cytology: In(3LR)61C6-7;100A-B; only the left end
  recovered.
 new order:: 100F - 100B|61C7 - 100.
 origin: X ray induced in oocytes.
 genetics: Result of a pericentric inversion followed by an
  exchange or of a translocation between 3L of
  one chromatid and 3R of its sister or homolog.
#
In(3LR)M-54C: Inversion (3LR) Minute-54c
 cytology: In(3L)73A9-10;75D7-E1 +
  In(3LR)61C2-3;80C4-5;93B4-5;100B8-9.
 new order:: 61A - 61C2|93B5 - 100B8|80C5 -
  93B4|80C4 - 75E1|73A10 - 75D7|73A9
  - | - | - 61C3|100B9 - 100F.
  Also carries an inversion with unspecified
  breakpoints in the region between 61C3 and 73A9.
 origin: Neutron induced.
 discoverer: Mickey, 54c10.
 references: 1963, DIS 38: 29.
 genetics: Mutant or deficient for M(3)54c and st.
#
In(3LR)P88
 cytology: In(3LR)61A;89C-D; deficient for bands in
  89C-D.
 origin: X ray induced.
 discoverer: E. B. Lewis, 55h.
 genetics: Deficient for ss but not bx.
#
In(3LR)sep: Inversion (3LR) separated
 cytology: In(3LR)65E;85E (Lewis, 1951, DIS 25: 108-9).
 discoverer: Muller.
 genetics: Mutant for sep. Also carries ri and
  p[P], which can be removed only with great
  difficulty.
#
In(3LR)TM1: Inversion (3LR) Third Multiple
 cytology: In(3L)63C;72E1-2 + In(3LR)69E;91C +
  In(3R)89B;97D.
 new order:: 61 - 63C|72E1 - 69E|91C - 97D|89B
  - 72E2|63C - 69E|91C - 89B|97D
  - 100.
 origin: Derived from T(2;3)Me/ri, presumably by a double
  crossover with exchanges in regions 72E2-80 and
  81-89B, which replaced the T(2;3) breakpoint in
  3 with ri.
 discoverer: E. B. Lewis.
 references: 1949, DIS 23: 92.
  1953, DIS 27: 58.
 genetics: Carries Me, ri, and sbd[l].
 genetics: Used as a balancer for chromosome 3, described
  as TM1 in the section on balancers.
#
In(3LR)TM3
 cytology: In(3LR)71C;94D-F + In(3LR)76C;93A +
  In(3LR)79E;100C superimposed on X[D]3[P] from
  T(1;3)1A8-B1;61A1-2 + In(3LR)65E;85E +
  In(3R)92D1-E1;100F2-3.
 new order:: 1A1 - 1A8|61A2 - 65E|85E -
  79E|100C - 100F2|92D1 - 85E|65E -
  71C|94D - 93A|76C - 71C|94F -
  100C|79E - 76C|93A - 92E1|100F3 -
  100F5.
 origin: Induced by repeated irradiation of the X[D]3[P]
  element of T(1;3)sc[260-20], which carried
  In(3LR)sep + In(3R)C, y[+] ri p sep bx[34e] e[s].
 discoverer: E. B. Lewis.
 references: Mitchell, 1958, Cold Spring Harbor Symp. Quant. Biol. 23: 279-90.
  Lewis, 1960, DIS 34: 51.
 genetics: Used as a balancer for chromosome 3, described
  as TM3 in the section on balancers.
#
In(3LR)TM6
 cytology: In(3LR)74;94 superimposed on In(3L)63C;72E1-2
  + In(3LR)61A;89CD + In(3R)92D1-E1;100F2-3.
 new order:: 61A|89C - 74|94 - 100F2|92D1 -
  89D|61A - 63C|72E1 - 63C|72E2 -
  74|94 - 92E1|100F3 - 100F5.
 origin: X ray induced in In(3L)P + In(3LR)P88 + In(3R)C,
  bx[34e] e.
 discoverer: E. B. Lewis and F. Bacher, 66i.
 genetics: Homozygous lethal. Deficiency for ss but not
  bx associated with In(3LR)P88.
 genetics: Used as a balancer for chromosome 3. Described
  as TM6 in section on balancers.
#
In(3LR)Ubx[101]: Inversion (3LR) Ultrabithorax
 cytology: In(3LR)80;89D9-E1.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1947.
 references: 1949, DIS 23: 59.
 genetics: Mutant for Ubx.
#
In(3LR)Ubx[130]
 cytology: In(3LR)61A-C;74;89D-E;93B;96A.
 new order:: 61A|96A - 93B|89D - 74|61C -
  74|89E - 93B|96A - 100.
 origin: X ray induced in e[s].
 discoverer: E. B. Lewis.
 references: 1952, Proc. Natl. Acad. Sci. U.S. 38: 955-60.
  1952, DIS 26: 66.
 genetics: Mutant for Ubx; homozygous lethal. Also
  carries e[s].
 genetics: A useful balancer for chromosome 3, described
  as TM2 in the section on balancers.
#
In(3LR)Ubx[A]
 origin: X ray induced.
 discoverer: Schalet, 1959.
 references: 1960, DIS 34: 53, 55.
 genetics: Mutant for Ubx; homozygous lethal. One
  breakpoint in 3L between h and st and
  another left of e (probably at Ubx).
#
In(3R)300.96
 cytology: In(3R)89F2-90A1;99B2-4.
 origin: X ray induced simultaneously with e[300.96].
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Carries an independent mutant for e. Homozygous
  viable but male sterile.
#
In(3R)Antp[B] Inversion (3R) Antennapedia of Bacon
 cytology: In(3R)84A;85E.
 origin: X ray induced.
 discoverer: Bacon, 50g.
 references: Lewis, 1956, DIS 30: 76.
 genetics: Mutant for Antp.
#
In(3R)Antp[LC] Inversion (3R) Antennapedia of Le Calvez
 cytology: In(3R)84A5-6;92A5-6.
 origin: Neutron induced.
 discoverer: Le Calvez.
 references: 1948, Bull. Biol. France Belg. 82: 97-113 (fig.).
 genetics: Associated with Antp[LC].
#
In(3R)Antp[R] Inversion (3R) Antennapedia of Rappaport
 cytology: In(3R)83F;86C (Ben-Zeev).
 origin: X ray induced.
 discoverer: Rappaport, 1963.
 references: Falk, 1964, DIS 39: 60.
 genetics: Associated with Antp[R].
#
In(3R)C
 cytology: In(3R)92D1-E1;100F2-3 |idges and Li in Morgan,
  Bridges, and Schultz, 1937, Carnegie Inst. Wash. Year
  Book 36: 301).
 origin: Naturally occurring inversion.
 discoverer: Sturtevant, 13f.
 synonym: C3, CIIIRE; In(3R)E.
 references: 1913, Science 37: 990-92.
  1917, Proc. Natl. Acad. Sci. U.S. 3: 555-58.
  1926, Biol. Zentr. 46: 697-702.
  1931, Carnegie Inst. Wash. Publ. No. 421: 1-27.
  Muller, 1918, Genetics 3: 422-99.
 genetics: Homozygous viable. Crossing over in 3R reduced
  to 1% between centromere and ss, to 0.2% between
  ss and e; no crossovers between e and
  tip of 3R recovered except for rare doubles
  within inversion.
 genetics: First inversion demonstrated genetically (Sturtevant,
  1926). Used as a balancer for the region from Dl
  to 3R tip. Balancers contain Sb, e, l(3)a,
  or l(3)e. Balancer for all of chromosome 3
  made by combining with In(3L)P. Found in wild
  populations (e.g., Oshima and Watanabe, 1965, DIS
  40: 88).
#
In(3R)C133: Inversion (3R) Crossover suppressor
 cytology: In(3R)93F;97C-D2.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygote rarely survives. Recombination between
  st and ca sharply reduced.
#
In(3R)C208
 cytology: In(3R)91B;96B.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable with wings held at 45[o] angle
  from body axis.
#
In(3R)ca[v]: Inversion (3R) claret-variegated
 cytology: In(3R)81F;99C-E.
 origin: X ray induced.
 discoverer: E. B. Lewis.
 genetics: Variegates for ca.
#
In(3R)Cyd: Inversion (3R) Curlyoid
 discoverer: Jollos.
 references: Curry, 1939, DIS 12: 46.
 genetics: Associated with Cyd.
 genetics: May be In(3R)P.
#
In(3R)Dl[B]: Inversion (3R) Delta-Barish
 cytology: In(3R)90A;91A (Schultz).
 discoverer: Schultz, 1933.
 genetics: Mutant for Dl.
#
In(3R)e[100.265]: Inversion (3R) ebony
 cytology: In(3R)93B5-6;95E.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for e; homozygous viable.
#
In(3R)hp: Inversion (3R) humped
 cytology: Breakpoints unknown.
 origin: Spontaneous.
 discoverer: Bridges, 31a22.
 genetics: Associated with hp.
#
In(3R)Hu: Inversion (3R) Humeral
 cytology: In(3R)84B2-3;84F2-3;86B4-C1.
 new order:: 61 - 84B2|84F2 - 84B3|86B4 -
  84F3|86C1 - 100.
 origin: X ray induced.
 discoverer: Ruch, 1931.
 genetics: Associated with Hu.
#
In(3R)J
 cytology: In(3R)96E;98F.
 origin: Naturally occurring inversion.
 discoverer: Oshima and Watanabe.
 references: 1965, DIS 40: 88.
#
In(3R)K: Inversion (3R) of Kodani
 cytology: In(3R)86F1-87A1;96F11-97A1.
 origin: Spontaneous.
 discoverer: Kodani.
#
In(3R)M: Inversion (3R) of Mourad
 cytology: In(3R)86F;100E.
 origin: Spontaneous.
 discoverer: Mourad and Mallah.
 references: 1960, Evolution 14: 166-70.
#
In(3R)Mo: Inversion (3R) from Missouri
 cytology: In(3R)93D;98F2-3 |idges and Li in Morgan,
  Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 293).
 origin: Naturally occurring inversion.
 discoverer: Sturtevant, 1924.
 references: 1931, Carnegie Inst. Wash. Publ. No. 421: 6-7.
 genetics: Crossing over reduced in heterozygote to about 5%
  between centromere and sr and 0.3% between sr
  and ca.
 genetics: Found in natural populations (e.g., Warters, 1944,
  Texas Univ. Publ. 4445: 129-74; Oshima and
  Watanabe, 1965, DIS 40: 88).
#
In(3R)Msc: Inversion (3R) Multiple sex comb
 cytology: In(3R)84B;84F.
 origin: Spontaneous.
 discoverer: Tokunaga, 64a.
 references: 1966, DIS 41: 57.
 genetics: Associated with Msc.
#
In(3R)Na: Inversion (3R) from Naples
 cytology: In(3R)86F2-3;96F11-97A1;97A2-5. 97A1-2 missing.
 new order:: 61 - 86F2|96F11 - 86F3|97A5 - 100.
 origin: Spontaneous.
 discoverer: Carfagna and Nicoletti, 1960.
 references: 1963, DIS 38: 32.
 genetics: Carries a lethal, which may be separable from
  inversion or the deficiency for 97A1-2 may be the
  lethal.
 genetics: Breakpoints similar to those of In(3R)K =
  In(3R)86F1-87A1;96F11-97A1 and may be the same.
#
In(3R)Nel-D: Inversion (3R) of Nel
 cytology: In(3R)86D;97A.
 origin: Spontaneous in natural population.
 discoverer: Nel.
 genetics: Possibly the same as In(3R)K =
  In(3R)86F1-87A1;96F11-97A1.
#
In(3R)p[100.290]: Inversion (3R) pink
 cytology: In(3R)85B3-4;85D12-15.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for p.
#
In(3R)P: Inversion (3R) of Payne
 cytology: In(3R)89C2-3;96A18-19 [Bridges and Bridges,
  1938, Genetics 23: 111-14 (fig.)].
 origin: Widespread in natural populations.
 discoverer: Payne, 17g.
 references: 1918, Indiana Univ. Studies 5, No. 36: 1-45.
  1924, Genetics 9: 327-42.
  Sturtevant, 1931, Carnegie
  Inst. Wash. Publ. No. 421: 1-27.
 genetics: Crossing over reduced in heterozygous female to 1%
  between p and sr, none between sr and
  ro, and 0.5% between ro and ca.
 genetics: Widespread in laboratory stocks and is part of the
  balancers, LVM and C(3)x. Also found in
  many wild populations (e.g., Warters, 1944, Texas
  Univ. Publ. 4445: 129-74; Oshima and Watanabe,
  1965, DIS 40: 88).
#
In(3R)sr[3.2]: Inversion (3R) stripe
 cytology: In(3R)90D1-E1;93B-E.
 origin: X ray induced.
 discoverer: Alexander, 1959.
 references: 1960, Genetics 45: 1019-22.
 genetics: Mutant for sr.
#
In(3R)su(pr): Inversion (3R) suppressor of purple
 cytology: Breakpoints unknown.
 origin: Spontaneous.
 discoverer: Stern, 27c2.
 synonym: su[S]-pr.
 references: 1929, Z. Induktive Abstammungs- Vererbungslehre 52: 373-89.
  1934, DIS 1: 35.
 genetics: Associated with su(pr).
#
In(3R)W: Inversion (3R) of Warters
 cytology: In(3R)86B;92F.
 origin: Naturally occurring inversion.
 discoverer: Warters.
 references: 1944, Texas Univ. Publ. 4445: 129-74.
#
R(1)1: Ring (1)
 cytology: R(1)1A;20B-C; salivary chromosomes show
  deficiency for most of 1A and a duplication
  for 20C-D [Schultz and Catcheside, 1937,
  J. Genet. 35: 315-20 (fig.)]. Ring shaped in metaphase.
 new order:: |1A - 20.20F - 20C|.
 origin: Spontaneous from C(1)RM, y female.
 discoverer: L. V. Morgan, 1922.
 synonym: X[c]; X[O].
 references: 1926, Proc. Natl. Acad. Sci. U.S. 12: 180-81.
  1933, Genetics 18: 250-83.
 genetics: Carries y. Male and homozygous female have
  reduced viability; X/0 male lethal (Schultz,
  1941, Proc. Intern. Congr. Genet., 7th.,
  pp. 257-62). Somewhat unstable, tending to be eliminated
  during mitosis. Shows about 5 times as much
  somatic crossing over as rod X |own, Walen,
  and Brosseau, 1962, Genetics 47: 1573-79).
  Crossing over reduced in ring/rod heterozygote; only
  double crossovers recovered. Exceptional males
  result from 4-strand double crossing over in
  R(1)1/+ female.
 genetics: Tends to open out into a rod [e.g., In(1)EN]
  spontaneously in stock.
#
R(1)2
 cytology: R(1)1A3-4;19F-20A1; salivary chromosomes
  deficient for 1A1-3 and duplicated for all of
  region 20 [Schultz and Catcheside, 1937,
  J. Genet. 35: 315-20 (fig.)]. Ring shaped in metaphase.
 new order:: |1A4 - 20.20F -
  20A1|.
 origin: Spontaneous as a detachment of C(1)RM, y[+].
 discoverer: Beadle, 34b (ring nature discovered by Boche).
 synonym: X[c2].
 genetics: Carries y[+]. More viable than R(1)1; X/0
  male survives. Ordinarily, ring elimination less
  than 1% (Battacharya, 1950, Proc. Roy. Soc. Edinburgh,
  B 64: 199-215; Braver and Blount, 1950,
  Genetics 35: 98), but nearly 20% of the first
  progeny of 11-day-old females crossed to
  ring-bearing males are gynandromorphs (Hannah, 1955,
  Z. Induktive Abstammungs- Vererbungslehre 86: 600-21).
  Crossing over reduced in ring/rod heterozygote; only
  double crossovers recovered. Exceptional males
  result from 4-strand double exchange in R(1)2/+
  female.
 genetics: Ring may open out spontaneously in stock [e.g.,
  In(1)EN2].
#
R(1)9-1
 cytology: Ring shaped in mitotic figures. Early prophase
  shows heterochromatic constitution (proceeding from
  normally proximal euchromatin, across the
  centromere to the normally distal euchromatin) to be
  as follows: a large segment, a well-defined
  constriction, a large segment, a constriction, a
  small segment, the centric constriction, a small
  segment.
 origin: Regular product of exchange in C(1)TMB[S]9-1.
 discoverer: Lindsley and Sandler, 1963.
 references: 1965, Genetics 51: 223-45 (fig.).
 genetics: Carries y. R(1)9-1/0 male survives. On basis
  of origin, R(1)9-1 is euchromatically but not
  heterochromatically identical with R(1)1.
#
R(1)9-4
 cytology: Ring shaped in mitotic figures. Early prophase
  shows heterochromatic constitution (proceeding from
  normally proximal euchromatin, across the centromere
  to the normally distal euchromatin) to be as
  follows: a large segment, a constriction, a small segment,
  the centric constriction, a small segment.
 origin: Regular product of exchange in C(1)TMB[S]9-4.
 discoverer: Lindsley and Sandler, 1963.
 references: 1965, Genetics 51: 223-45 (fig.).
 genetics: Carries y. R(1)9-4/0 male viable. Based on
  origin, R(1)9-4 euchromatically but not
  heterochromatically identical with R(1)1.
#
R(1)63
 cytology: Ring shaped in mitotic figures. Early prophase
  shows heterochromatic constitution (proceeding from
  the normally proximal euchromatin, across the
  centromere to the normally distal euchromatin) to be
  as follows: two large segments separated by an
  ill-defined constriction, a constriction, a small
  segment, the centric constriction, a small segment.
 origin: Regular product of exchange in C(1)TM2.
 discoverer: Lindsley and Sandler, 63g.
 references: 1965, Genetics 51: 223-45 (fig.).
 genetics: Carries y. R(1)63/0 male survives. Based on
  origin, R(1)63 is euchromatically but not
  heterochromatically identical with R(1)1.
#
R(1)94-2A1
 cytology: R(1)1A;1F-2A;5E-6A;17F-18A;20; duplicated for
  1A-F and 18A-20.
 new order:: |1A - 5E|1F -
  1A|20.20 - 6A|18A -
  20|.
 origin: Spontaneous product of C(1)94-2A. Possibly a
  product of breakage of double second-anaphase
  bridge formed by exchange between the arms of the
  compound.
 discoverer: Armentrout, 1964.
#
R(1)C1
 cytology: Ring shaped in mitotic figures.
 origin: Spontaneous derivative of In(1)sc[8L]EN[R];
  arose by recombination between distal
  heterochromatic segment of In(1)sc[8] and
  heterochromatic short arm of In(1)EN.
 discoverer: Lindsley, 1950.
 references: 1958, Z. Induktive Abstammungs- Vererbungslehre
  89: 103-22.
 genetics: Carries y. On basis of origin, R(1)C1 is
  euchromatically identical with R(1)1, but it
  must be different heterochromatically since
  R(1)C1/0 male viable.
#
R(1)l-v459
 cytology: R(1)3D-F.
 origin: Associated with T(1;2;3)l-v459.
#
R(1)y[4]: Ring (1) yellow
 cytology: R(1)1A8-B1;18A3-4; deficient for 1A and
  duplicated for 18-20.
 new order:: |1B1 - 20.20 - 18A4|.
 origin: Regular product of exchange within inversion in
  C(1)RM heterozygous for In(1)y[4] =
  In(1)1A8-B1;18A3-4.
 discoverer: Sturtevant and Beadle.
 references: 1936, Genetics 21: 554-604.
  Novitski and Sandler, 1956, Genetics 41: 194-206.
 genetics: Deficient for l(1)J1, duplicated for car-bb.
  Heterozygous female survives; male lethal, owing to
  deficiency for l(1)J1.
#
R(Y)
  See Y Derivatives in Special Special Chromosomes Chromosomes section.
#
T(1;?)sc[260-23]: Translocation (1;?) scute
 cytology: T(1;?)1B2-3; position of second break not
  determined.
 origin: X ray induced.
 discoverer: Sutton, 1939.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y or svr.
#
T(1;Y)1
 cytology: T(1;Y)16F;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y)2
 cytology: T(1;Y)5E;11F;19F;Y[S]
 new order:: 1 - 5E|Y[SP] - Y[L];
  20 - 19F|11F - 5E|19F - 11F|Y[SD].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)3
 cytology: T(1;Y)3E;Y[S].
 origin: X ray induced in y/y[+]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)4
 cytology: T(1;Y)11A;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)6
 cytology: T(1;Y)11D;Y[S].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)8
 cytology: T(1;Y)4B;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)9
 cytology: T(1;Y)2C;19F;Y[S].
 new order:: 1A - 2C|Y[SP] - Y[L];
  20 - 19F|2C - 19F|Y[SD].
 origin: X ray induced in y/y[+]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y)10
 cytology: T(1;Y)3E;Y[L].
 origin: X ray induced in y/y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)11
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)13
 cytology: T(1;Y)7D;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)14
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)15
 cytology: T(1;Y)14F;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)16
 cytology: T(1;Y)4C;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)18
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)19
 cytology: T(1;Y)17A;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)20
 cytology: T(1;Y)11A;Y[L].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y)21
 cytology: T(1;Y)1F;Y[L].
 origin: X ray induced in y/y[+]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y)22
 cytology: T(1;Y)19E;Y[S].
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)100
 cytology: T(1;Y)13F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)101
 cytology: T(1;Y)19E;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)102
 cytology: T(1;Y)7D;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)103
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)104
 cytology: T(1;Y)3D;Y[L].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)105
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)106
 cytology: T(1;Y)16A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)107
 cytology: T(1;Y)3C;Y[L].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)108
 cytology: T(1;Y)5D;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)111
 cytology: T(1;Y)3C;Y[L].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal. Variegates for w and N.
#
T(1;Y)112
 cytology: T(1;Y)15A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)113
 cytology: T(1;Y)20A;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)114
 cytology: T(1;Y)3C;Y[L].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)115
 cytology: T(1;Y)8F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)117
 cytology: T(1;Y)17A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)118
 cytology: T(1;Y)16E;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)119
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)120
 cytology: T(1;Y)17E;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)122
 cytology: T(1;Y)20A;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)123
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)124
 cytology: T(1;Y)9F;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)125
 cytology: T(1;Y)15D;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with or without a free Y.
#
T(1;Y)128
 cytology: T(1;Y)3C;Y[L].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)129
 cytology: T(1;Y)11A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)131
 cytology: T(1;Y)6E;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22
  (fig.).
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)132
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)133
 cytology: T(1;Y)19E;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)135
 cytology: T(1;Y)18C;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)137
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)139
 cytology: T(1;Y)20A;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)140
 cytology: T(1;Y)3C;Y[L].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)141
 cytology: T(1;Y)19E;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)142
 cytology: T(1;Y)13E;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22
  (fig.).
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)145
 cytology: T(1;Y)11B;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y)147
 cytology: T(1;Y)8F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)148
 cytology: T(1;Y)2D;Y[L].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)149
 cytology: T(1;Y)6E;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)150
 cytology: T(1;Y)3F;Y[S].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y)151
 cytology: T(1;Y)19F;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)152
 cytology: T(1;Y)13A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)155
 cytology: T(1;Y)7B;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)156
 cytology: T(1;Y)7D;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)157
 cytology: T(1;Y)14F;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)158
 cytology: T(1;Y)11A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)159
 cytology: T(1;Y)18A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)164
 cytology: T(1;Y)3C;Y[L].
 origin: X ray induced in B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y)169
 cytology: T(1;Y)11D;Y[S].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and fertile with or without a free Y.
#
T(1;Y)240
 cytology: T(1;Y)14A;Y[L].
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable; fertile with a free Y and sterile
  without.
#
T(1;Y)290
 cytology: T(1;Y)1A;20A;Y[S].
 new order:: 1A|Y[SP] - Y[L];
  20F- 20A|1A - 20A|Y[SD].
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y;2)7
 cytology: T(1;Y)14F;Y[S] + T(Y;2)Y[L];36C.
 new order:: 1 - 14F|Y[SP] - Y[LP]|36C - 21;
  20 - 14F|Y[SD];
  Y[LD]|36C - 60.
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y;2)17
 cytology: T(1;Y;2)7B;Y[L];39.
 new order:: 1 - 7B|39 - 60;
  20 - 7B|Y[LD];
  Y[S] - Y[LP]|39 - 21.
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;2)109
 cytology: T(1;Y;2)3C;Y[L];40-41; involvement of
  chromosome 2 inferred from genetic data; not
  cytologically observable; new order therefore
  ambiguous.
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22
  (fig.).
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;2)110
 cytology: T(1;2)19D;55F + T(Y;2)Y[S];45F.
 new order:: 1 - 19D|55F - 45F|Y[SP] - Y[L];
  20 - 19D|55F - 60;
  Y[SD]|45F - 21.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;2)130
 cytology: T(1;Y;2)11F;Y[L];40-41; involvement of
  chromosome 2 inferred from genetic data; not
  cytologically observable; new order therefore
  ambiguous.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22
  (fig.).
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;2)146
 cytology: T(1;Y)7D;Y[L] + T(1;2)20A;57F.
 new order:: 1 - 7D|Y[LP] - Y[S];
  20F - 20A|57F - 60;
  Y[LD]|7D - 20A|57F - 21.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;2)153
 cytology: T(1;Y;2)17A;Y[S];35D.
 new order:: 1 - 17A|35D - 60;
  20 - 17A|Y[SD];
  Y[L] - Y[SP]|35D - 21.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y;2)160
 cytology: T(1;Y;2)17C;Y[S];40-41; involvement of
  chromosome 2 inferred from genetic data; not
  cytologically observable; new order therefore
  ambiguous.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;3)5
 cytology: T(1;Y)11D;Y[L] + T(1;3)14F;72.
 new order:: 1 - 11D|Y[LP] - Y[S];
  20 - 14F|72 - 61;
  Y[LD]|11D - 14F|72 - 100.
 origin: X ray induced in y[+]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;3)121
 cytology: T(1;Y;3)6F;Y[S];86D.
 new order:: 1 - 6F|Y[SP] - Y[L];
  20 - 6F|86D - 100;
  Y[SD]|86D - 61.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y;3)127
 cytology: T(1;Y;3)19F;Y[S];85E.
 new order:: 1 - 19F|85E - 61;
  20 - 19F|Y[SD];
  Y[L] - Y[SP]|85E - 100.
 origin: X ray induced.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;3)134
 cytology: T(1;Y)12E;Y[S] + T(1;3)19E;62A.
 new order:: 1 - 12E|Y[SP] - Y[L];
  20F - 19E|62A - 61;
  Y[SD]|12E - 19E|62A - 100.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;3)136
 cytology: T(1;Y;3)7A;Y[L];70C.
 new order:: 1 - 7A|70C - 100;
  20 - 7A|Y[LD];
  Y[S] - Y[LP]|70C - 61.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;3)138
 cytology: T(1;Y;3)11A;Y[L];84B.
 new order:: 1 - 11A|84B - 61;
  20 - 11A|Y[LD];
  Y[S] - Y[LP]|84B - 100.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;3)143
 cytology: T(1;Y)12A;Y[L] + T(1;3)3F;69C.
 new order:: 1 - 3F|69C - 100;
  20 - 12A|Y[LD];
  Y[S] - Y[LP]|12A - 3F|69C - 61.
 origin: X ray induced in y/B[S]Y sperm.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable with a free Y and sterile. Male
  lethal without a free Y.
#
T(1;Y;3)144
 cytology: T(1;Y;3)15E;Y[L];74D.
 new order:: 1 - 15E|74D - 100;
  20 - 15E|Y[LD];
  Y[S] - Y[LP]|74 - 61.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable with a free Y and sterile. Male
  lethal without a free Y.
#
T(1;Y;3)154
 cytology: T(1;Y;3)10A;Y[S];97A.
 new order:: 1 - 10A|97A - 61;
  20 - 10A|Y[SD];
  Y[L] - Y[SP]|97A - 100.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;Y;3)161
 cytology: T(1;Y;3)17A;Y[L];94.
 new order:: 1 - 17A|94 - 61;
  20 - 17A|Y[LD];
  Y[S] - Y[LP]|94 - 100.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male lethal.
#
T(1;Y;4)116
 cytology: T(1;Y)14D;Y[S] + T(1;4)9C;101.
 new order:: 1 - 9C|101;
  20 - 14D|Y[SD];
  Y[L] - Y[SP]|14D - 9C|102.
 origin: X ray induced in B[S]Y.
 discoverer: Nicoletti.
 references: Nicoletti and Lindsley, 1960, Genetics 45: 1705-22.
  1960, DIS 34: 95-97.
 genetics: Male viable and sterile.
#
T(1;2)7
 origin: X ray induced.
 discoverer: Bonner, 1931.
 references: Dobzhansky, 1935, Z. Induktive Abstammungs-
  Vererbungslehre 68: 134-62.
 genetics: X broken between rb and cv;
  chromosome 2 to the right of sp. Male and
  heterozygous female viable and fertile; homozygous
  female poorly viable and sterile. X[P]2[D]
  recoverable as an aneuploid segregant that is
  duplicated for the loci of y through rb but
  is not demonstrably deficient for 2R markers;
  nothing written to indicate that it is deficient for
  M(2)c.
#
T(1;2)26
 origin: X ray induced in R(1)2.
 discoverer: Pontecorvo, 1941.
 synonym: T(X[c2];2)26.
 references: 1942, DIS 16: 65.
 genetics: Section of X including car and bb
  inserted into base of 2L. Homozygous lethal.
#
T(1;2)51
  b
 cytology: T(1;2)3C1-2;3D6-7;20A;52F.
 new order:: 1 - 3C1|20A - 3D7|20A - 20F;
  21 - 52F|(3C2 - 3D6)|52F - 60.
 origin: X ray induced in In(1)w[m4] = In(1)3C1-2;20A.
 discoverer: Lefevre, 51b7.
 synonym: T(1;2)w[+51b7].
 references: 1951, DIS 25: 71.
  1952, DIS 26: 66.
  Ratty, 1954, Genetics 39: 513-28.
 genetics: Segregant Dp(1;2)51b = Dp(1;2)3C1-2;3D6-7;52F
  survives; duplicated for loci of w, rst, spl,
  fa, and dm. Duplication used to cover lethality
  of N in studies of pseudoallelism at the N
  locus (Welshons and Von Halle, 1962, Genetics
  47: 743-59).
#
T(1;2)106
 origin: X ray induced.
 discoverer: Sturtevant, 1930.
 genetics: Break in X chromosome near centromere to right
  of f; break in chromosome 2 near
  centromere, probably in 2L. Male fertile;
  homozygous female viable and fertile. Crossing over
  and disjunction for both chromosomes X and 2
  normal in T(1;2)106/+ female.
  T(1;2)106/+/Y female shows nondisjunction of
  X's.
#
T(1;2)260-31
 cytology: T(1;2)9A;24;29.
 new order:: 1 - 9A|(24 - 29)|9A - 20;
  21 - 24|29 - 60.
 origin: X ray induced simultaneously with y[260-31].
 discoverer: Fano, 1941.
 references: Sutton, 1943, Genetics 28: 210-17.
 genetics: Male lethal; lethality attributable to the
  independent mutation to y[260-31] since
  T(1;2)260-31, y[260-31]/Df(1)sc[260-25] is
  lethal.
#
T(1;2)271b
 cytology: T(1;2)3C3-7;40; inferred from
  figs. 15A, G, and H of Mackensen (1935).
 origin: X ray induced.
 discoverer: Patterson.
 synonym: Df(1)Del271b.
 references: 1932, Am. Naturalist 66: 193-206.
  Mackensen, 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Mutant for N.
#
T(1;2)A50b: Translocation (1;2) from Austin
 cytology: T(1;2)2B;15F;41; inferred from fig. 17H of
  Mackensen (1935).
 new order:: 1 - 2B|15F - 20;
  21 - 41|15F - 2B|41 - 60.
 references: Mackensen, 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Left break in X between br and pn;
  right break between r and f. Mutant for
  f.
#
T(1;2)A61b
 cytology: T(1;2)15F; breakpoint in chromosome 2 at
  unknown position in left arm, which also carries an
  inversion. Breakpoint in X inferred from
  fig. 17G of Mackensen (1935).
 references: Mackensen, 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Mutant for f.
#
T(1;2)A106
 cytology: T(1;2)6-7;12;17; rough estimates of
  breakpoints in X from fig. 17I of Mackensen
  (1935); chromosome 2 broken in euchromatin of
  left arm.
 new order:: 1 - 6|17 - 20;
  21 - ?|12 - 17|7 - 12|? - 60.
 references: Mackensen,1935, J. Heredity 26: 163-74 (fig.).
 genetics: Mutant for Bx.
#
T(1;2)A124
 cytology: T(1;2)10A;13A1-2;59.
 new order:: 1 - 10A|13A2 - 20;
  21- 59|(10A - 13A1)|59 - 60.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1934.
 references: Mackensen, 1935, J. Heredity 26: 163-74 (fig.).
  Patterson, Stone, and Bedichek, 1935, Genetics
  20: 259-79 (fig.).
  1937, Genetics 22: 407-26.
  Pipkin, 1940, Texas Univ. Publ. 4032; 126-56.
 genetics: Left break between ras and v; right break
  between g and pl. Male fertile. The
  segregant Dp(1;2)A124 = Dp(1;2)10A;13A1-2;59,
  which is duplicated for v[+] through g[+],
  survives as fairly viable and fertile female, but
  male carrying Dp(1;2)A124 dies as embryo. The
  complementary Df(1)A124 = Df(1)10A;13A1-2
  survives as a fertile X/X/Df triploid female and
  as an X/X/Df diploid metafemale but not as an
  X/Df diploid.
#
T(1;2)B[48g]: Translocation (1;2) Bar
 cytology: T(1;2)15F-16A1;33B superimposed on
  In(1)1B3-4;19F-20C1.
 new order:: 1A1 - 1B3|19F - 16A1|33B - 60;
  20F - 20C1|1B4 - 15F|33B - 21.
 origin: X ray induced in In(1)sc[4].
 discoverer: Yu, 48g.
 genetics: Position effect at B. Male sterile.
#
T(1;2)B[bd]: Translocation (1;2) Bar-baroid
 cytology: T(1;2)16A1-2;48C2-3 + In(2R)41A;47A |idges in
  Morgan, Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 291).
 new order:: 1 - 16A1|48C2 - 47A|41A - 47A|41A
  - 21;
  20 - 16A2|48C3 - 60.
 origin: X ray induced simultaneously with In(2R)41-47.
 discoverer: Dobzhansky, 31b5.
 references: 1932, Genetics 17: 369-92.
 genetics: Recessive position effect for B. Translocation
  and inversion probably not separable.
#
T(1;2)B[DG] Translocation (1;2) Bar of Dubinin and Goldat
 cytology: T(1;2)4;15F-16A;20;40-41; inferred from
  figure of Dubinin and Goldat.
 new order:: 1 - 4|15F - 4|20;
  21 - 40|(16A - 20)|41 - 60.
 origin: X ray induced.
 discoverer: Dubinin and Goldat, 1936.
 references: 1936, Biol. Zh. (Moscow) 5: 881-84 (fig.).
 genetics: Position effect for B. Male lethal.
#
T(1;2)Bld: Translocation (1;2) Blond
 cytology: T(1;2)1C3-4;60B12-13 + In(2R)42A2-3;58A4-B1.
 new order:: 1A - 1C3|60B12 - 58B1 |42A3 -
  58A4|42A2 - 21;
  20 - 1C4|60B13 - 60F.
 origin: Spontaneous in In(2R)Cy.
 discoverer: Burkart, 1930.
 references: 1931, Rev. Fac. Argon. Vet. Univ. Buenos Aires
  7: 393-491.
  Burkart and Stern, 1933, Z. Induktive Abstammungs-
  Vererbungslehre 64: 310-25.
  Bridges, 1937, Cytologia (Tokyo), Fujii Jub.,
  Vol. 2: 745-55.
  Morgan, Bridges, and Schultz, 1938, Carnegie
  Inst. Wash. Year Book 37: 307.
 genetics: Associated with Bld. Both aneuploid segregants
  survive. The X[D]2[P] element is duplicated for
  y, ac, sc, Hw, svr, su(s), l(1)7e, su(b), and
  M(1)Bld and deficient for sp, bs, ba, Pin, and
  M(2)c; heterozygote extreme Plexate and slight
  Minute with small dark body and slow development;
  viability low; male sterile; female slightly
  fertile. 2[D]X[P] is reciprocally
  duplicate deficient; heterozygous female Blond and
  extreme Minute [M(1)Bld] with short, broad,
  occasionally downward-curved wings; ecloses 3-4 days
  late; male lethal.
#
T(1;2)C6 Translocation (1;2) Crossover suppressor
 cytology: T(1;2)12E;40-41;60B; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 new order:: 1 - 12E|41 - 60B|40 - 21;
  20 - 12E|60B - 60F.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Male lethal. Recombination reduced in 2R.
#
T(1;2)C20
 cytology: T(1;2)12E;30B.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Male viable and sterile. Recombination reduced in
  2L.
#
T(1;2)C54
 cytology: T(1;2)12E;32F.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Male lethal. Recombination reduced in 2L.
#
T(1;2)C60
 cytology: T(1;2)20;52B.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Male viable and fertile. Recombination reduced in
  2R.
#
T(1;2)C84
 cytology: T(1;2)3F;17E-F;30A.
 new order:: 1 - 3F|17F - 20;
  21 - 30A|3F - 17E|30A - 60.
 origin: X ray induced.
 discoverer: Roberts and D. Stewart, 1964.
 genetics: Male viable and sterile. Recombination reduced in
  X and 2L.
#
T(1;2)C121
 cytology: T(1;2)20;35F;40.
 new order:: 1 - 20|(35F - 40)|20;
  21 - 35F|40 - 60.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and fertile. Recombination reduced in
  2L.
#
T(1;2)C171
 cytology: T(1;2)12A;40-41.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and sterile. Recombination reduced in
  X chromosome.
#
T(1;2)C176
 cytology: T(1;2)20;40-41 + In(1)8C-D;18D; translocation
  breakpoint in chromosome 2 with respect to
  centromere not determined; new order therefore
  ambiguous.
 new order:: 1 - 8C|18D - 8D|18D - 20|40 - 60;
  20|40 - 21.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in X
  chromosome. Tentative.
#
T(1;2)C179
 cytology: T(1;2)9A;49A + In(1)5C;20.
 new order:: 1 - 5C|20 - 9A|49A - 21;
  20|5C - 9A|49A - 60.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in X
  chromosome.
#
T(1;2)C183
 cytology: T(1;2)12E;40-41 + In(2L)24C;30A; translocation
  breakpoint in chromosome 2 with
  respect to centromere not determined; new order therefore ambiguous.
 new order:: 1 - 12E|40 - 60;
  20 - 12E|40 - 30A|24C - 30A|24C - 21.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in 2L.
#
T(1;2)C239
 cytology: T(1;2)7A-B;36C;39E.
 new order:: 1 - 7A|36C - 39E|7B - 20;
  21 - 36C|39E - 60.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in X
  chromosome. The segregant Dp(2;1)C239 =
  Dp(2;1)7A-B;36C;39E survives.
#
T(1;2)C256
 cytology: T(1;2)2A;40-41 + In(1)7E;17A;18B; position of
  breakpoint with respect to centromere in
  chromosome 2 not determined; new order therefore
  ambiguous. For example, if chromosome 2 is
  broken in 2L:
 new order:: 1 - 2A|40 - 60;
  20 - 18B|17A - 18B|7E - 17A|7E - 2A|40
  - 21.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in X
  chromosome.
#
T(1;2)C261
 cytology: T(1;2)14C;40-41; breakpoint in
  chromosome 2 with respect to centromere not determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and sterile. Recombination reduced in
  X chromosome.
#
T(1;2)C262
 cytology: T(1;2)11A;18A;40-41; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 new order:: 1 - 11A|40 - 60;
  20 - 18A|11A - 18A|40 - 21.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in X
  chromosome
#
T(1;2)C314
 cytology: T(1;2)5D;40-41 + T(1;2)9D;51D + T(1;2)20;56F;
  position of left breakpoint in chromosome 2
  with respect to centromere not determined.
 new order:: 1 - 5D|40 - 51D|9D - 5D|40 - 21;
  20|56F - 51D|9D - 20|56F - 60.
  Tentative because heterochromatic realignments
  ambiguous.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and sterile. Recombination reduced in
  X and 2R.
#
T(1;2)C324
 cytology: T(1;2)15F;20;30A.
 new order:: 1 - 15F|20 - 15F|30A - 60;
  20|30A - 21.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Mutant or deficient for f. Male lethal.
  Recombination reduced in 2L.
#
T(1;2)C349
 cytology: T(1;2)6C;47D + In(1)2E;20.
 new order:: 1 - 2E|20 - 6C|47D - 21;
  20|2E - 6C|47D - 60.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in X
  chromosome.
#
T(1;2)C357
 cytology: T(1;2)20;56F.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and sterile. Recombination reduced in
  2R.
#
T(1;2)ct[7a1]: Translocation (1;2) cut
 cytology: T(1;2)7B; other breakpoints not recorded.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 1947.
 genetics: Mutant for ct but not y, ac, sc, cm, sn, or
  oc. Male lethal.
#
T(1;2)ct[7c1]
 cytology: T(1;2)7B2-3;8E2-3;25C superimposed on
  R(1)1A3-4;19F-20A1.
 new order:: |1A4 - 7B2|8E2 - 20.20F
  - 20A1|;
  21 - 25C|(7B3 - 8E2)|25C - 60.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 1947.
 genetics: Mutant for ct but not cm or sn; male
  lethal. T(1;2)ct[7c1]/Dp(1;3)sn[13a1] male
  survives and is fertile. The segregant
  Dp(1;2)ct[7c1] = Dp(1;2)7B2-3;8E2-3;25C
  survives; duplicated for sn but not cm;
  male and female have darker, roof-like wings,
  enlarged abdomens, and are sterile.
#
T(1;2)ct[14a2]
 cytology: T(1;2)7B2-4;19-20;41E1-2 superimposed on
  R(1)1A3-4;19F-20A1.
 new order:: |1A4 - 7B2|20.20F -
  20A1|;
  21 - 41E1|7B4 - 19|41E2 - 60.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 1947.
 genetics: Mutant for ct but not cm, sn, or oc.
  Male lethal. T(1;2)ct[14a2]/Dp(1;3)sn[13a1] male
  rarely survives, probably sterile.
#
T(1;2)ct[268-17]
 cytology: T(1;2)7B2-5;41E2-4 (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 34h.
 genetics: Mutant for ct but not scp or sn. Male
  lethal.
#
T(1;2)ct[268-24]
 cytology: T(1;2)7B2-5;41F6-42A1.
 origin: X ray induced.
 discoverer: Hoover, 35i.
 genetics: Mutant for ct but not scp or sn. Male
  lethal.
#
T(1;2)ct[268-26]
 cytology: T(1;2)7B3-C1;36E.
 origin: X ray induced.
 discoverer: Hoover, 35j.
 genetics: Mutant for ct but not scp or sn. Male
  lethal.
#
T(1;2)ct[268-32]
 cytology: T(1;2)1E-F;3D-E;7B2-5;46 (Hoover).
 new order:: 1A - 1E|3E - 7B2|46 - 21;
  20 - 7B5|3D - 1F|46 - 60.
 origin: X ray induced in y.
 discoverer: Demerec, 38e.
 genetics: Mutant for ct but not fa, dm, scp, or
  sn. Male lethal.
#
T(1;2)ct[268-33]
 cytology: T(1;2)7B2-5;41E (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 38e.
 genetics: Mutant for ct but not sn. Male lethal.
#
T(1;2)ct[268-41]
 cytology: T(1;2)7B2-5;37C2-3 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39l.
 genetics: Mutant for ct but not cm or sn. Male
  lethal.
#
T(1;2)D1: Translocation (1;2) from deoxycytidine
 cytology: T(1;2)6F;26C.
 origin: Induced by tritiated deoxycytidine.
 discoverer: Kaplan, 1965.
 references: 1966, DIS 41: 59.
 genetics: Male lethal.
#
T(1;2)D2
 cytology: T(1;2)8B;46B.
 origin: Induced by tritiated deoxycytidine.
 discoverer: Kaplan, 1965.
 references: 1966, DIS 41: 59.
 genetics: Male lethal.
#
T(1;2)ef: Translocation (1;2) elfin
 cytology: T(1;2)14C8-D1;2R.
 origin: Induced by triethylenemelamine (CB. 1246).
 discoverer: Fahmy, 1952.
 references: 1959, DIS 33: 86.
 genetics: Mutant for ef. Male sterile.
#
T(1;2)f[257-15]: Translocation (1;2) forked
 cytology: T(1;2)13E9-10;15E2-3;24F (Sutton).
 new order:: 1A - 13E9|15E3 - 20;
  21 - 24F|(13E10 - 15E2)|24F - 60.
 origin: X ray induced.
 discoverer: Demerec, 35a.
 genetics: Mutant for f but not M(1)o or B. Male
  lethal.
#
T(1;2)f[257-22]
 cytology: T(1;2)4D2-3;8F;15E4-F1;39E;41F-42A superimposed
  on Dp(1;1)15F9-16A1;16A7-B1.
 new order:: 1 - 4D2|(8F - 15E4)|41F - 39E|(4D3
  - 8F)|39E - 21;
  20 - 16A1|16A7 - 16A1|16A7 - 15F1|42A - 60.
 origin: X ray induced in y B[i]B[i].
 discoverer: Demerec, 36c.
 genetics: Mutant for f but B unaffected. Male lethal.
#
T(1;2)K1: Translocation (1;2) of Krivshenko
 cytology: T(1;2)1A5-B3;20;29A-B; deficient for 1B3-20.
 new order:: 1A1 - 1A5|29B - 60;
  20|29A - 21.
 origin: X ray induced.
 discoverer: Krivshenko, 56c12.
 references: 1956, DIS 30: 75.
 genetics: Homozygous lethal. Fly hyperploid for the
  2L[D]X[P] element survives.
#
T(1;2)l-v25: Translocation (1;2) lethal-variegated
 cytology: T(1;2)19-20;40-41; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male sterile.
#
T(1;2)l-v47
 cytology: T(1;2)8F-9B; heterochromatic material inserted
  in X; genetic results suggest linkage between
  X and 2.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; gg-like phenotype.
#
T(1;2)l-v75
 cytology: T(1;2)19-20;41.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male sterile.
#
T(1;2)l-v129
 cytology: T(1;2)18B;41.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a semilethal; male sterile.
#
T(1;2)l-v135
 cytology: T(1;2)18-19;41.
 origin: X ray induced simultaneously with T(2;3)135 =
  T(2;3)37;85A, which has been lost.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal.
#
T(1;2)l-v150
 cytology: T(1;2)16-17;40.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male sterile.
#
T(1;2)l-v219
 cytology: T(1;2)10A;40.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male sterile.
#
T(1;2)l-v223
 cytology: T(1;2)14F;41;50E.
 new order:: 1A - 14F|(41 - 50E)|14F - 20;
  21A - 41|50E - 60.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1640-70.
 genetics: Variegated for a lethal and has defective external male
  genitalia; male sterile.
#
T(1;2)lt: Translocation (1;2) light
 cytology: T(1;2)20C-D;40F.
 origin: X ray induced in chromosome carrying eq.
 discoverer: Schultz.
 genetics: Variegated for lt.
#
T(1;2)lt[m16]: Translocation (1;2) light-mottled
 cytology: T(1;2)11A;12F;22D;40B-F.
 new order:: 1 - 11A|12F - 20;
  21 - 22D|11A - 12F|40B - 22D|40F - 60.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(1;2)lt[m31]
 cytology: T(1;2)8F;28D;40B-F.
 new order:: 1 - 8F|28D - 40B|8F - 20;
  21 - 28D|40F - 60.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(1;2)lz: Translocation (1;2) lozenge
 cytology: T(1;2)8D12-E1;33A-B (Hannah).
 origin: X ray induced.
 discoverer: Green and Green.
 references: 1956, Z. Induktive Abstammungs- Vererbungslehre
  87: 708-21.
 genetics: Mutant for lz.
#
T(1;2)N[264-9]: Translocation (1;2) Notch
 cytology: T(1;2)3C;41. Cytology not examined; breakpoints
  inferred from genes affected (Schultz).
 origin: X ray induced.
 discoverer: Demerec, 33l5.
 genetics: Variegates for rst, N, dm, and, at low
  temperatures, w; also variegates for abnormal
  abdomen and M(2)S2 but not stw, ap, or
  msf (Schultz).
#
T(1;2)N[264-10]
 origin: X ray induced.
 discoverer: Demerec, 33l.
 genetics: Variegates for rst, N, and dm but not w.
  Carries normal alleles of M(2)S2, ap, msf, and
  tk (Schultz). X/Y male lethal; X/Y/Y
  survives.
#
T(1;2)N[264-23]
 cytology: T(1;2)3C8-9;41A (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 35h.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-102.
 genetics: Variegates for rst and fa but not w or
  dm.
#
T(1;2)N[264-24]
 cytology: T(1;2)3C8-9;40F (Demerec).
 origin: X ray induced.
 discoverer: Demerec, 35h.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Variegates for w, rst, and fa.
#
T(1;2)N[264-50]
 cytology: T(1;2)3C7-9;20C1-F;22A2-3 (Hoover).
 new order:: 1 - 3C7|20F;
  21 - 22A2|3C9 - 20C1|22A3 - 60.
 origin: X ray induced.
 discoverer: Demerec, 37k.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Variegates for fa but not w, rst, or dm.
#
T(1;2)N[264-53]
 cytology: T(1;2)3C6-7;34C7-D1.
 origin: X ray induced.
 discoverer: Demerec, 38a.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Carries normal alleles of rst, fa, and dm.
#
T(1;2)N[264-59]
 cytology: T(1;2)3C8-9;40F (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 38d.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Variegates for w, rst, and spl but not pn,
  kz, or dm.
#
T(1;2)N[264-62]
 cytology: T(1;2)3C7-8;41A-B (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 38e.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Variegates for w, rst, and fa but not dm.
#
T(1;2)N[264-66]
 cytology: T(1;2)3C6-7;41 + T(1;2)7C9-D1;53F (Hoover).
 new order:: 1 - 3C6|41 - 53F|7D1 - 20;
  21 - 41|3C7 - 7C9|53F - 60.
 origin: X ray induced.
 discoverer: Demerec, 38e.
 genetics: Variegates for w, rst, fa, dm, and ec but
  not pn, kz, or bi.
#
T(1;2)N[264-69]
 cytology: T(1;2)3C7-8;44C4-5 (Demerec).
 origin: X ray induced.
 discoverer: Demerec, 38k.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Carries a mutant allele of N and normal alleles
  of w, rst, and dm.
#
T(1;2)N[264-80]
 cytology: T(1;2)3C6-7;36;40 + In(1)11;20 (Sutton).
 new order:: 1 - 3C6|(36 - 40)|3C7 - 11|20 -
  11|20;
  21 - 36|40 - 60.
 origin: X ray induced.
 discoverer: Demerec, 39d.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Contains mutant allele of N but normal alleles
  of w, rst, dm, and ec.
#
T(1;2)N[264-82]
 cytology: T(1;2)3C3-4;41A + T(1;2)20A;57.
 new order:: 1 - 3C3|41A - 57|20A - 20F;
  21 - 41A|3C4 - 20A|57 - 60.
  Tip of 2L also in chromocenter (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39d.
 genetics: Variegates for w, rst, fa, and dm but not
  pn, ec, or bi.
#
T(1;2)N[264-102]
 cytology: T(1;2)3C6-7;50E;56C (Sutton).
 new order:: 1 - 3C6|(50E - 56C)|3C7 - 20;
  21 - 50E|56C - 60.
 discoverer: Demerec, 39l.
 genetics: Carries mutant allele of N and normal alleles of
  w, rst, and dm.
#
T(1;2)OR6: Translocation (1;2) from Oak Ridge
 cytology: T(1;2)2A;60D.
 origin: X ray induced in y.
 discoverer: Warters, 1959.
 genetics: Male viable and fertile. Homozygous female viable.
  X[D]2[P] element can replace one
  chromosome 2, producing a deficiency for the tip of 2R;
  resulting progeny are Minute owing to inclusion of
  M(2)c locus in the deficiency.
#
T(1;2)OR7
 cytology: T(1;2)3A;41E.
 origin: X ray induced in y.
 discoverer: Warters, 1959.
 genetics: Male lethal. Male survives with B[S]w[+]Y but
  is sterile.
#
T(1;2)OR8
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1959.
 genetics: Male viable and fertile. Homozygous female viable.
#
T(1;2)OR9
 cytology: T(1;2)3A;14F;41.
 new order:: 1 - 3A|14F - 20;
  21 - 41|14F - 3A|41 - 60.
 origin: X ray induced in y.
 discoverer: Warters, 1959.
 genetics: Male lethal; lethality not covered by
  B[S]w[+]Y; therefore, probably associated with
  break at 14F.
#
T(1;2)OR11
 cytology: T(1;2)14F;41.
 origin: X ray induced.
 discoverer: Warters, 1959.
 genetics: Variegated for a lethal. X/Y male viable and
  sterile.
#
T(1;2)OR14
 cytology: T(1;2)18D;46B.
 origin: X ray induced.
 discoverer: Warters, 1959.
 genetics: Male quite inviable; rare survivor has unexpanded
  wings and crossed scutellars.
#
T(1;2)OR15
 cytology: T(1;2)11B;60E.
 origin: X ray induced.
 discoverer: Warters, 1959.
 genetics: Male viable and sterile.
#
T(1;2)OR17
 cytology: T(1;2)3C;37C.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile, has either a normal Y
  or B[S]w[+]Y.
#
T(1;2)OR18
 cytology: T(1;2)20B;30E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. 2L[D]X[P] element
  recoverable in viable hyperploids with outstretched
  wings.
#
T(1;2)OR19
 cytology: T(1;2)20;51F + In(2R)42B;48E;57C.
 new order:: 1 - 20|51F - 48E|57C - 51F|20;
  21 - 42B|48E - 42B|57C - 60E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and weakly fertile. Homozygous female
  viable. Dp(2;1)OR19 = Dp(2;1)20;48E;51F;57C
  survives in both male and female.
#
T(1;2)OR20
 cytology: T(1;2)16C;43B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal; lethal originated after translocation.
#
T(1;2)OR21
 cytology: T(1;2)19E;32D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR22
 cytology: T(1;2)8D;22B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR23
 cytology: T(1;2)6B;40.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR25
 cytology: T(1;2)1B;38E.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR26
 cytology: T(1;2)15A;41.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile; X/0 male has
  melanotic, distended wings.
#
T(1;2)OR27
 cytology: T(1;2)16D;34B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR28
 cytology: T(1;2)3B;39E.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile, has either a normal Y
  or B[S]w[+]Y.
#
T(1;2)OR29
 cytology: T(1;2)8D;40.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR30
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR32
 cytology: T(1;2)20;54A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  2R[D]X[P] element survives.
#
T(1;2)OR33
 cytology: T(1;2)17;47A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR36
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR37
 cytology: T(1;2)10A;50C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR38
 cytology: T(1;2)20B;50A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal. Male hyperploid for the 2R[D]X[P]
  element probably survives.
#
T(1;2)OR39
 cytology: T(1;2)1D;46E.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR41
 cytology: T(1;2)12D;25E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR42
 cytology: T(1;2)12F;58F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR43
 cytology: T(1;2)15E;40D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile, has small rough eyes,
  possibly mutant for un.
#
T(1;2)OR44
 cytology: T(1;2)16F;28F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR45
 cytology: T(1;2)7D;40-41; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR47
 cytology: T(1;2)19E;53B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR48
 cytology: T(1;2)17A;31F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR49
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR50
 cytology: T(1;2)19C;33F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile. Homozygous female weakly
  viable.
#
T(1;2)OR51
 cytology: T(1;2)8D;41F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal; lethal originated after translocation.
#
T(1;2)OR52
 cytology: T(1;2)4F;41A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR54
 cytology: T(1;2)19E;32E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile, has slightly curled wings.
#
T(1;2)OR55
 cytology: T(1;2)20A;44D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR56
 cytology: T(1;2)18F;47D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR58
 cytology: T(1;2)11B;40-41 + T(1;2)19C;30B; position of
  right breakpoint in chromosome 2 with respect
  to centromere not determined.
 new order:: 1 - 11B|40 - 30B|19C - 11B|41 - 60;
  20 - 19C|30B - 21.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal. Male hyperploid for 2L[D]X[P]
  element survives and has outstretched wings.
#
T(1;2)OR59
 cytology: T(1;2)19E;57B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal. Male hyperploid for the 2R[D]X[P]
  element survives.
#
T(1;2)OR60
 cytology: T(1;2)10A;52D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR61
 cytology: T(1;2)18D;31F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR62
 cytology: T(1;2)8F;17F;40-41; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 new order:: 1 - 8F|40 - 60;
  20 - 17F|8F - 17F|40 - 21.
  Tentative.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR64
 cytology: T(1;2)11A;53F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR65
 cytology: T(1;2)7A;40.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR66
 cytology: T(1;2)8B;23C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile.
#
T(1;2)OR67
 cytology: T(1;2)12B;41 + T(1;2)20A;45B.
 new order:: 1 - 12B|41 - 45B|20A;
  21 - 41|12B - 20A|45B - 60.
  Tentative.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Variegated for a lethal. Male fertile.
#
T(1;2)OR68
 cytology: T(1;2)16E;41 + Tp(2)25E;33A;40.
 new order:: 1 - 16E|41 - 40|(25E - 33A)|40
  - 33A|25E - 21;
  20 - 16E|41 - 60.
  Tentative.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR69
 cytology: T(1;2)3C;41C.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Variegated for a lethal; male sterile, has either a
  normal Y or B[S]w[+]Y.
#
T(1;2)OR72
 cytology: T(1;2)19E;29F + In(2LR)24F;54B.
 new order:: 1 - 19E|29F - 54B|24F - 21;
  20 - 19E|29F - 24F|54B - 60.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for the
  2R[D]2L[M]X[P] element may survive.
#
T(1;2)OR73
 cytology: T(1;2)19E;57E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for the
  2R[D]X[P] element survives.
#
T(1;2)OR74
 cytology: T(1;2)19E;56C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  2R[D]X[P] element survives.
#
T(1;2)OR75
 cytology: T(1;2)12E;32B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR78
 cytology: T(1;2)19E;30B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  2L[D]X[P] element survives and has outstretched
  wings.
#
T(1;2)OR82
 cytology: T(1;2)13D;30B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR83
 cytology: T(1;2)12A;22B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2)OR84
 cytology: T(1;2)3C;38E.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile, has either a normal Y
  or B[S]w[+]Y.
#
T(1;2)OR85
 cytology: T(1;2)10;38.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)OR86
 cytology: T(1;2)11A;32B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2)ret: Translocation (1;2) reticulated
 cytology: T(1;2)20A5-B2;2R.
 origin: Induced by
  L-p-N,N-di-(2-chloroethyl)aminophenylalanine
  (CB. 3025).
 discoverer: Fahmy, 1953.
 references: 1958, DIS 32: 73.
 genetics: Associated with ret; male sterile.
#
T(1;2)sc[19]: Translocation (1;2) scute
 cytology: T(1;2)1B1-2;1B4-7;25-26; breaks in X
  estimated from fig. 1 of Muller and Prokofyeva (1934,
  Dokl. Akad. Nauk. n.s. 4: 74-83), but the left
  break (which genetically is to the left of y) is
  inconsistent with the cytological location of y
  in region 1A5-8. Break in chromosome 2
  estimated from position of y[+] 1-2 units to
  the right of dp.
 new order:: 1A - 1B1|1B7 - 20;
  21 - 25|(1B2 - 1B4)|26 - 60.
 origin: X ray induced.
 discoverer: League.
 references: Muller, 1935, Genetica 17: 237-52.
 genetics: Mutant for sc. A small subterminal piece of
  X is inserted into 2L 1 or 2 units to the
  right of dp. The two halves of the translocation
  are recoverable independently as Df(1)sc[19] =
  Df(1)1B1-2;1B4-7 and Dp(1;2)sc[19] =
  Dp(1;2)1B1-2;1B4-7;25-26. Df(1)sc[19] is
  deficient for y, ac, sc, and l(1)sc but not
  l(1)J1, om, or M(1)Bld; it is male lethal
  but survives in the heterozygous female.
  Dp(1;2)sc[19] carries, in addition to
  sc[19], normal alleles of y, ac, and
  l(1)sc; it is viable homozygous and does not
  affect crossing over in 2L.
#
T(1;2)sc[115]
 cytology: T(1;2)1A6-B1;25F; inferred from fig. 3
  of Goldat.
 origin: X ray induced derivative of sc[6].
 discoverer: Goldat.
 references: 1936, Biol. Zh. (Moscow) 5: 803-12.
 genetics: Mutant for sc.
#
T(1;2)sc[260-17]
 cytology: T(1;2)1B2-3;31C.
 origin: X ray induced.
 discoverer: Sutton, 39d.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y, ac, or svr.
#
T(1;2)sc[260-26]
 cytology: T(1;2)1B4-5;41F2-3;58B2-3 + In(2LR)27D2-3;41A.
 new order:: 1A - 1B4|41F3 - 58B2|1B5 - 20;
  21 - 27D2|41A - 27D3|41A - 41F2|58B3
  - 60.
 origin: X ray induced.
 discoverer: Sutton, 39l.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y, ac, or svr.
#
T(1;2)sc[260-27]
 cytology: T(1;2)15E;33-34;57B-C + Dp(1;f)1A8-B1;19F.
 new order:: 1A1 - 1A8|19F - 20;
  21 - 33|15E - 19F|1B1 - 15E|57B - 34|57C
  - 60.
 origin: X ray induced.
 discoverer: Sutton, 39l.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y, ac, or svr.
  Male sterile. Dp(1;f)sc[260-27] =
  Dp(1;f)1A8-B1;19F segregates free from
  translocation, carries normal alleles of y and
  ac.
#
T(1;2)sc[S2] Translocation (1;2) scute of Sinitskaya
 cytology: T(1;2)1B4-7;60C-E (inferred from genetic
  results).
 discoverer: Sinitskaya, 1934.
 genetics: Mutant for sc. X chromosome broken to the right
  of l(1)sc in same place as right breakpoint of
  T(1;2)sc[19] and 2R broken between sp and
  M(2)c x ller). Aneuploid segregants
  X[D]2[P] and 2R[D]X[P] should survive.
  T(1;2)SP1: Translocation (1;2) from So'a~'o Paulo T(1;2)SP1: Translocation (1;2) from So'a~'o Paulo
 cytology: T(1;2)8B;41.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Variegated for a lethal; male sterile.
#
T(1;2)SP4
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP10
 cytology: T(1;2)10;50.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP16
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP18
 cytology: T(1;2)1A;56A.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP19
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP20
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP31
 cytology: T(1;2)20;56B.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for the
  2R[D]X[P] element survives.
#
T(1;2)SP33
 cytology: T(1;2)14;41.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP36
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP42
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP43
 cytology: T(1;2)16A;60C.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP48
 cytology: T(1;2)15F;35A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP49
 cytology: T(1;2)12;40-41; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP50
 cytology: T(1;2)20;29-30.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  2L[D]X[P] survives.
#
T(1;2)SP51
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP52
 cytology: T(1;2)12E;57F.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP55
 cytology: T(1;2)1A;41 + T(1;2)4B;30B + In(1)12D;14B.
 new order:: 1A|41 - 30B|4B - 1A|41 - 60;
  20 - 14B|12D - 14B|12D - 4B|30B - 21.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male lethal.
#
T(1;2)SP58
 cytology: T(1;2)10A;34A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP60
 cytology: T(1;2)17E;35A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP61
 cytology: T(1;2)18F;47D.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP64
 cytology: T(1;2)3C;28C.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile, has either a normal Y
  or B[S]w[+]Y.
#
T(1;2)SP67
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP69
 cytology: T(1;2)7C;41.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP71
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP75
 cytology: T(1;2)8C;35D.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP77
 cytology: T(1;2)9A;41.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP81
 cytology: T(1;2)20;24F-25A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  2L[D]X[P] element survives.
#
T(1;2)SP84
 cytology: T(1;2)4C;42C.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP87
 cytology: T(1;2)9A4-B1;58A3-4.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP88
 cytology: T(1;2)20;32F-33A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for the
  2L[D]X[P] element survives.
#
T(1;2)SP89
 cytology: T(1;2)4E;35A.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. May be mutant for rg.
#
T(1;2)SP93
 cytology: T(1;2)18C-D;22A-B.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for the
  2L[D]X[P] element survives.
#
T(1;2)SP94
 cytology: T(1;2)14B-C;23F.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP96
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP97
 cytology: T(1;2)9E-F;35A-B.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP102
 cytology: T(1;2)16A;41.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP106
 cytology: T(1;2)6B;40.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP110
 cytology: T(1;2)13A;57E.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)SP111
 cytology: T(1;2)20;40-41; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2)Sy: Translocation (1;2) Stubby
 origin: Spontaneous.
 discoverer: Ives, 34j31.
 genetics: Associated with Sy. Male sterile. Probably
  reciprocal translocation with breaks near the base
  of X and 2L.
#
T(1;2)v[267-4]: Translocation (1;2) vermilion
 cytology: T(1;2)11A7-8;36 (Sutton).
 origin: X ray induced.
 discoverer: Hoover, 35i.
 genetics: Mutant for v |eakpoint not at v locus).
  Semilethal. ras, dwx, sbr, m, dy, and fw
  not affected.
#
T(1;2)w[13G2]: Translocation (1;2) white
 cytology: T(1;2)3C3-5;56F; also inversion in 2R.
 origin: X ray induced.
 discoverer: Gans.
 genetics: Variegated for w.
#
T(1;2)w[m52b12]: Translocation (1;2) white-mottled
 cytology: T(1;2)1E5-F1;3C3-4;20B;40-41.
 new order:: 1A - 1E5|20B - 3C4|20B - 20F;
  21 - 40|(1F1 - 3C3)|41 - 60.
 origin: X ray induced in In(1)rst[3] = In(1)3C3-4;20B.
 discoverer: Ratty, 52b12.
 references: Lefevre, 1953, DIS 27: 57.
 genetics: Variegated for w. Dp(1;2)w[m52b12] =
  Dp(1;2)1E5-F1;3C3-4;40-41 survives.
#
T(1;2)w[m53a]
 cytology: T(1;2)3B2-C1;3C9-D1;40-41.
 new order:: 1 - 3B2|3D1 - 20;
  21 - 40|(3C1 - 3C9)|41 - 60.
 origin: X ray induced.
 discoverer: P. Farnsworth, 53a4.
 references: Lefevre, 1953, DIS 27: 57.
 genetics: Variegated for w. The segregant
  Dp(1;2)w[m53a] = Dp(1;2)3B2-C1;3C9-D1;40-41
  survives and is duplicated for the loci of w,
  rst, and N. Df(1)w[m53a] = Df(1)3B2-C1;3C9-D1
  survives as Notch female; deficient for w, rst,
  and N.
#
T(1;2)w[m53e]
 cytology: T(1;2)3C3-4;20A2-3;58F8-59A1.
 new order:: 1 - 3C3|58F8 - 21;
  20F - 20A3|3C4 - 20A2|59A1 - 60.
 origin: Neutron induced.
 discoverer: Mickey, 53e11.
 synonym: T(Xv'-.25m'.v'.25m'2)In[X and 3].
 references: 1963, DIS 38: 29.
 genetics: Variegated for w.
#
T(1;2)w[m258-34]
 cytology: T(1;2)3C3-5;41A (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 38b.
 genetics: Variegated for w but not rst, fa, or dm.
  Male viable.
#
T(1;2)w[m258-36]
 cytology: T(1;2)3C6-7;4C2-3;41A-B;41F5-6 (Demerec and
  Hoover).
 new order:: 1 - 3C6|(41B - 41F5)|4C3 - 20;
  21 - 41A|(3C5 - 4C2)|41F6 - 60.
  Insertions said to be in inverted order but not
  specified with respect to centromere or numerical
  order.
 origin: X ray induced.
 discoverer: Demerec, 38b.
 references: Sutton, 1940, Genetics 25: 534-40 (fig.).
 genetics: Variegated for w and rst but not pn, fa,
  or dm. Male viable. Cytology predicts that
  each element of the translocation should survive as
  aneuploid but not so recorded.
#
T(1;2)w[m258-37]
 cytology: T(1;2)3C3-4;40-41A (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 33j.
 genetics: Variegated for w but not kz, rst, fa, or
  dm.
#
T(1;2)w[m258-39]
 cytology: T(1;2)3C3-5;40E-F (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 38e.
 genetics: Variegated for w but not pn, rst, fa, or
  dm. Male viable.
#
T(1;2)w[m258-40]
 cytology: T(1;2)3C3-5;41 (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 38e.
 genetics: Variegated for w and rst but not pn, kz,
  fa, or dm.
#
T(1;2)w[mD1] Translocation (1;2) white-mottled of Dubinin
 cytology: T(1;2)3B;19-20;21F.
 new order:: 1 - 3B|21F - 60;
  20|3B - 19|21F - 21A.
 origin: X ray induced.
 discoverer: Dubinin.
 references: Sacharov, 1936, Biol. Zh. (Moscow) 5: 293-302.
#
T(1;2)w[vD4] Translocation (1;2) white-variegated of Demerec
 cytology: T(1;2)3D6-E1;40F (Schultz).
 origin: X ray induced.
 discoverer: Demerec, 33k2.
 genetics: Variegated for N, rst, w, and dm. X/Y male
  survives only rarely as rst with mottled eye
  color; X/Y/Y male more viable, slightly rst,
  and sterile. Variegation for lt in X/X/Y
  female.
#
T(1;2)w-ec: Translocation (1;2) white-echinus
 cytology: T(1;2)3C1-2;3E7-8;37D.
 new order:: 1 - 3C1|3E8 - 20;
  21 - 37D|(3C2 - 3E7)|37D - 60.
 origin: X ray induced.
 references: Lefevre and Wilkins, 1966, Genetics 53: 175-87.
 genetics: T(1;2)w-ec male is phenotypically white and
  echinus; N not affected. Does not complement
  with w[sp]. Gives rise to Df(1)w-ec.
#
T(1;2)y[260-13]: Translocation (1;2) yellow
 cytology: T(1;2)1A4-5;36D.
 origin: X ray induced.
 discoverer: Sutton, 1939.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for y.
#
T(1;2)y[v1]: Translocation (1;2) yellow-variegated
 cytology: T(1;2)1A;39.
 origin: X ray induced.
 discoverer: Schultz, 33a11.
 genetics: Variegated for y.
#
T(1;2;3)58i
 origin: X ray induced.
 discoverer: Imazumi.
 references: 1961, DIS 35: 87-88.
  1962, DIS 36: 80.
  1962, Cytologia 27: 212-28 (fig.).
 genetics: Distal one-third of 2L appended to X
  chromosome as short arm. Also T(2;3) with
  2R broken between cn and vg and 3L
  broken between se and st. Male lethal in
  embryo.
#
T(1;2;3)220
 cytology: T(1;2;3)14A;50A;75C.
 new order:: 1 - 14A|50A - 21;
  20 - 14A|75C - 61;
  60 - 50A|75C - 100.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Male viable and sterile.
#
T(1;2;3)C232 Translocation (1;2;3) Crossover suppressor
 cytology: T(2;3)35D;71E; additional presence of
  T(1;2)20;40-41 or T(1;3)20;80-81 inferred
  from genetic data.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and fertile; homozygous female lethal.
  Recombination reduced in 2L.
#
T(1;2;3)C312
 cytology: T(2;3)32C;87E; additional presence of
  T(1;2)20;40-41 or T(1;3)20;80-81 inferred
  from genetic data.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male sterile. Recombination reduced in 2L.
#
T(1;2;3)ct[268-40]: Translocation (1;2;3) cut
 cytology: T(1;2;3)7D2-3;10A5-6;21B-C;28-29;40-41;75B-C;87D;88C;92;
  new order not determined.
 origin: X ray induced.
 discoverer: Demerec, 39k.
 references: Sutton, 1940, Genetics 25: 534-40 (fig.).
 genetics: Mutant at ct but not scp, cm, sn, v, sbr, dy,
  g, ty, na, pl, sd, or mc. Male lethal.
#
T(1;2;3)Din: Translocation (1;2;3) Dinty
 cytology: T(1;3)3C;63A + T(2;3)39D;73A (Lindsley).
 new order:: 1A - 3C|63A - 73A|39D - 60;
  20 - 3C|63A - 61;
  21 - 39D|73A - 100.
 origin: X ray induced.
 discoverer: Braver, 55a.
 references: 1955, DIS 29: 70.
  Pollock, 1963, DIS 38: 50.
 genetics: Associated with Din. Male viable and fertile.
  The two translocations should be easily separable,
  and Din is, in all probability, associated with
  only one.
#
T(1;2;3)l-v216 Translocation (1;2;3) lethal-variegated
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male sterile.
#
T(1;2;3)l-v459
 cytology: T(1;2;3)3D-F;XR;50;80-81.
 new order:: 1A - 3D|50 - 21;
  |3F - 20F.;
  20F.80 - 61;
  60 - 50.81 - 100.
  Tentative.
  Postulated that centromere of
  chromosome 3 split or double with one half capped
  by 2R[D] and the other by XR[D].
  X[P] in the form of a ring.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal; male fertile.
#
T(1;2;3)N[264-74]: Translocation (1;2;3) Notch
 cytology: T(1;2;3)3C10-11;20D-E;40C-D;92E6-8; 20D-E break
  claimed to be to the left of the nucleolus organizer
  (Sutton).
 new order:: 1 - 3C10|40D - 60;
  20F - 20E|40C - 21;
  61 - 92E6|20D - 3C11|92E8 - 100.
 origin: X ray induced.
 discoverer: Demerec, 38k.
 references: Sutton, 1940, Genetics 25: 534-40 (fig.).
 genetics: Variegates for w, rst, and N but not kz,
  pn, or dm.
#
T(1;2;3)N[264-87]
 cytology: T(1;2;3)3C7-9;10A2-B1;45F-46A;59F-60A;97C-D;100E-F
  (Sutton).
 new order:: 1 - 3C7|97D - 100E|59F - 46A|10B1
  - 20;
  21 - 45F|3C9 - 10A2|60A - 60F;
  61 - 97C|100F.
 origin: X ray induced.
 discoverer: Demerec, 39j.
 references: Sutton, 1940, Genetics 25: 534-40.
 genetics: Carries a mutant allele of N and normal alleles
  of w, rst, and dm.
#
T(1;2;3)OR9 Translocation (1;2;3) from Oak Ridge
 cytology: T(1;2;3)19-20;49F;81F.
 new order:: 1 - 19|81F - 61;
  20|49F - 60;
  21 - 49F|81F - 100.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2;3)OR10
 cytology: T(1;2;3)18A;41;73F.
 new order:: 1 - 18A|73F - 100;
  20 - 18A|41 - 60;
  21 - 41|73F - 61.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)OR12
 cytology: T(1;2)3A;41 + T(1;3)7E;78F.
 new order:: 1 - 3A|41 - 21;
  20 - 7E|78F - 61;
  60 - 41|3A - 7E|78F - 100.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile, has either a normal Y
  or B[S]w[+]Y.
#
T(1;2;3)OR14
 cytology: T(1;2;3)5E;21D;62C.
 new order:: 1 - 5E|21D - 60;
  20 - 5E|62C - 61;
  21A - 21D|62C - 100.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile. Homozygous female viable.
#
T(1;2;3)OR16
 cytology: T(1;2)1A;57D + T(1;3)29;72E.
 new order:: 1A|57D + T(1;3)20;72E.
 new order:: 1A|57D - 21;
  20|72E - 61;
  60 - 57D|1A - 20|72E - 100.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)OR17
 cytology: T(1;2;3)19;40-41;61F; neither breakpoints in
  X and 2 with respect to centromeres nor new
  order determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)OR23
 cytology: T(1;2;3)14C;27D;87B.
 new order:: 1 - 14C|87B - 61;
  20 - 14C|27D - 21;
  60 - 27D|87B - 100.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2;3)OR24
 cytology: T(1;2)14B;39D + T(1;3)2C;80C + T(1;3)29;87A.
 new order:: 1 - 2C|80C - 87A|19 - 14B|39D - 21;
  20 -19|87A - 100;
  60 - 39D|14B - 2C|80C - 61.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2;3)OR25
 cytology: T(1;2;3)19E;29B;80-81; position of breakpoint
  in chromosome 3 with respect to centromere not
  determined; new order therefore ambiguous.
 new order:: 1 - 19E|80 - 100;
  20 - 19E|29B - 21;
  60 - 29B|80 - 61.
  Tentative.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Hyperploid male,
  presumably carrying 2L[D]X[P], survives.
#
T(1;2;3)OR26
 cytology: T(1;2)2D;56F + T(1;3)3F;96B.
 new order:: 1 - 2D|56F - 21;
  20 - 3F|96B - 100;
  60 - 56F|2D - 3F|96B - 61.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile.
#
T(1;2;3)OR31
 cytology: T(1;3)20;92A + T(2;3)38D;87E.
 new order:: 1 - 20|92A - 87E|38D - 60;
  29|92A - 100;
  21 - 38D|87E - 61.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3R[D]X[P] element survives.
#
T(1;2;3)OR34
 cytology: T(1;3)18F;84B + T(2;3)28B;75F + T(2;3)44C;63A.
 new order:: 1 - 18F|84B - 75F|28B - 21;
  20 - 18F|84B - 100;
  60 - 44C|63A - 75F|28B - 44C|63A - 61.
  Tentative.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;2;3)sc[260-18]: Translocation (1;2;3) scute
 cytology: T(1;2)1A6-B1;41D-E + T(1;3)7A2-B1;80C.
 new order:: 1A1 - 1A6|41D - 21;
  20 - 7B1|80C - 61;
  60 - 41E|1B1 - 7A2|80C - 100.
 origin: X ray induced.
 discoverer: Sutton, 39d.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y, ac, or svr.
  Male sterile.
#
T(1;2;3)sc[260-29]
 cytology: T(1;2;3)1A6-B1;22A-B;34A-B;75C-E.
 new order:: 1A1 - 1A6|34A - 22B|34B - 60;
  20 - 1B1|75C - 61;
  21 - 22A|75E - 100.
 origin: X ray induced.
 discoverer: Sutton, 40a.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y, ac, or svr.
#
T(1;2;3)sc[P1] Translocation (1;2;3) scute of Panshin
 discoverer: Panshin, 1934.
 genetics: Mutant for sc.
  T(1;2;3)SP3: Translocation (1;2;3) from So'a~'o Paulo T(1;2;3)SP3: Translocation (1;2;3) from So'a~'o Paulo
 cytology: T(1;2;3)20;23A-B;96B.
 new order:: 1 - 20|96B - 61;
  20|23A - 21;
  60 - 23B|96B - 100.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male lethal. Male hyperploid for 2L[D]X[P]
  element survives.
#
T(1;2;3)SP5
 cytology: Six-break rearrangement with two breaks in 2R,
  one in 3L, and two in 3R.
 new order:: X[D]|2R[P] - 2L;
  X[P]|X[M]|3R[M]|3L[D];
  2R[D]|3L[P] - 3R[P]|3R[D].
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male sterile.
#
T(1;2;3)SP6
 cytology: T(1;2;3)20;40-41;80-81; neither positions of
  breakpoints with respect to centromeres nor new
  order determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)SP8
 cytology: T(1;2;3)5;17F;44B;90A.
 new order:: 1 - 5|17F - 20;
  21 - 44B|5 - 17F|90A - 100;
  61 - 90A|44B - 60.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)SP25
 cytology: T(1;2;3)19;54;86.
 new order:: 1 - 19|54 - 21;
  20 - 19|86 - 100;
  60 - 54|86 - 61.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
  Male hyperploid for 3R[D]X[P] apparently
  survives.
#
T(1;2;3)SP29
 cytology: T(1;2;3)10E-11A;40;60D;64D.
 new order:: 1 - 10E|40 - 60D|64D - 61;
  21 - 11A|60D - 60F;
  21 - 40|64D - 100.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)SP40
 cytology: T(1;2;3)4-5;50A;80 + T(2;3)40;86.
 new order:: 1 - 4|80 - 86|40 - 21;
  20 - 5|50A - 60;
  61 - 80|50A - 40|86 - 100.
  Tentative.
 origin: Gamma ray induced in y w.
 discoverer: Lindlsey and Musatti, 1961.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;2;3)SP57
 cytology: T(1;2;3)20;40-41;75A; breakpoint in
  chromosome 2 inferred from genetic data.
 new order:: 1 - 20|75A - 100;
  20|40 - 21;
  60 - 40|75A - 61.
  Tentative.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)SP65
 cytology: T(1;2;3)18A;39E;76A.
 new order:: 1 - 18A|76A - 100;
  20 - 18A |39E - 21;
  60 - 39E|76A - 61.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;2;3)w[m258-44] Translocation (1;2;3) white-mottled
 cytology: T(1;2;3)3C3-4;4D2-E1;56E1-F1;80D (Sutton).
 new order:: 1 - 3C3|80D - 100;
  20 - 4E1|80D - 61;
  21 - 56E1|(3C4 - 4D2)|56F1 - 60.
 origin: X ray induced.
 discoverer: Demerec, 38k.
 genetics: Variegated for w but not pn, rst, or fa.
  T(1;2;3)w[m258-44] may be separated into
  T(1;3)w[m258-44] = T(1;3)3C3-4;4D2-E1;80D, which
  is deficient for 3C4 through 4D2 (i.e.,
  Df(1)w[m258-44] = Df(1)3C3-4;4D2-E1), and
  Dp(1;2)w[m258-44] =
  Dp(1;2)3C3-4;4D2-E1;56E1-F1, which is duplicated
  for the same region. The deficiency includes the
  loci of fa, dm, M(1)3E, ec, M(1)4BC, bi, peb,
  and rb but not rst or rg. 3C3-4
  breakpoint inconsistent with genetic data on rst.
  Dp(1;2)w[m258-44] should be viable.
#
T(1;2;3)wy[274-2]: Translocation (1;2;3) wavy
 cytology: T(1;2)8F-9A;20A-B;26B-D + T(1;3)11D-E;65C-D
  (Sutton).
 new order:: 1 - 8F|26D - 60;
  20F - 20B|9A - 11D|65C - 61;
  21 - 26B|20A - 11E|65D - 100.
 origin: X ray induced.
 discoverer: Demerec, 34a.
 genetics: Mutant for wy but not fw, dy, g, or s.
  Male lethal.
#
T(1;2;3;4)l-v454 Translocation (1;2;3;4) lethal-variegated
 cytology: T(1;2;3)12B;22-23;81 + T(2;4)44F;101F.
 new order:: 1 - 12B|81 - 61;
  20 - 12B|22 - 21;
  60 - 44F|101F - 101A;
  100 - 81|23 - 44F|101F - 102.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Associated with l(1)v[454]. Male sterile.
#
T(1;2;4)A12: Translocation (1;2;4) from Austin
 cytology: T(1;2;4)1B-C;7A;7B;13B1-5;101-102; breakpoints
  in chromosomes 2 and 4 not determined
  (Mackensen, 1935, Texas Univ. Publ. 4032: frontispiece).
 new order:: 1A - 1B|13B5 - 20;
  21 - ?|(7A - 7B)|? - 60;
  101|((1C - 7A)|(7B - 13B1))|102.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedicheck, and Suche.
 references: Stone, 1934, Genetica 16: 506-19.
  Mackensen, 1935, J. Heredity 26: 163-74.
  Patterson, Stone, and Bedicheck, 1935, Genetics
  20: 259-79.
  1937, Genetics 22: 407-26.
 genetics: A section from between sc and br on the left
  to between g and sd on the right is inserted
  into chromosome 4. The ct locus, but not
  cm, sn, or oc, is deleted from the insertion
  [i.e., Df(1)A12 = Df(1)7A;7B] and inserted into
  chromosome 2 [i.e., Dp(1;2)A12 =
  Dp(1;2)7A;7B]. Female hyperploid for the
  X[D]X[P] element [i.e., Dp(1;f)A12 =
  Dp(1;f)1B-C;13B1-5] survives and is claimed to be
  fertile. Female hyperploid for X[M] [i.e.,
  Dp(1;4)A12 = Dp(1;4)1B-C;7A;7B;13B1-5;101-102]
  occasionally survives and is sterile.
#
T(1;2;4)N[264-85]: Translocation (1;2;4) Notch
 cytology: T(1;2;4)3B4-C1;6A2-B1;60A4-5;101F-102A [Sutton,
  1940, Genetics 25: 534-40 (fig.)].
 new order:: 1 - 3B4|60A4 - 21;
  29 - 6B1|60A5 - 60F;
  101A - 101F|(3C1 - 6A2)|102A - 102F.
 origin: X ray induced.
 discoverer: Demerec, 39d.
 genetics: Variegates for w, rst, fa, dm, rg, cx, cv, rux,
  and vs but not pn, ec, bi, peb, or rb.
  Carries normal allele of ci (Stern).
  Dp(1;4)N[264-85] =
  Dp(1;4)3B4-C1;6A2-B1;101F-102A viable in both
  sexes and sterile in male. Complementary
  Df(1)N[264-85] inviable.
#
T(1;2;4)OR24 Translocation (1;2;4) from Oak Ridge
 cytology: T(1;2)3C;38A + T(1;4)11A;102C.
 new order:: 1 - 3C|38A - 60;
  20 - 11A|102C - 102F;
  21 - 38A|3C - 11A|102C - 101A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Produces a hyperploid
  female that may carry the 4[D]X[P] element.
#
T(1;2;4)w[m]bw[V] Translocation (1;2;4) white- mottled brown-Variegated
 cytology: T(1;2)12F3-4;59C4-5 + T(1;4)3C3-4;101E4-5.
 new order:: 1 - 3C3|101E4 - 101A;
  20 - 12F4|59C5 - 60;
  21 - 59C4|12F3 - 3C4|101E5 - 102F.
 origin: Neutron induced.
 discoverer: Mickey, 53f15.
 references: 1963, DIS 38: 30.
 genetics: Variegated for w. Also claimed to variegate for
  bw, which is unusual since the T(1;2) is
  completely euchromatic.
#
T(1;2;4)w[vD2] Translocation (1;2;4) white-variegated of Demerec
 cytology: T(1;2;4)3C4-5;18F;38;101A-C (Schultz).
 new order:: 1 - 3C4|101C - 102F;
  20 - 18F|3C5 - 18F|38 - 21;
  60 - 38|101A.
  Tentative.
 origin: X ray induced.
 discoverer: Demerec, 33k27.
 genetics: Variegated for w but not rst in male and for
  w and occasionally rst in female.
  Absence of effect on ci a criterion for
  postulating break in 4L. Fly hyperploid for the
  X[D]4[P] element survives.
#
T(1;3)3
 origin: X ray induced.
 discoverer: Bonner, 1931.
 references: Dobzhansky, 1935, Z. Induktive Abstammungs-
  Vererbungslehre 68: 143-46.
 genetics: X chromosome broken between rb and rg;
  3R broken to the right of ca. Male and
  homozygous and heterozygous females viable and
  fertile. Crossing over in heterozygous female
  nearly absent in left end of X, rises to about
  normal around ct, and may be increased at right
  end. Crossing over in chromosome 3 in
  translocation heterozygote normal between e[s]
  and ro and reduced to two-thirds normal between
  ro and ca. Male carrying the X[D]3[P]
  element in place of a normal 3 nearly lethal;
  female has narrow wings, occipital bristles, and
  branched posterior veins. Crossing over between
  normal X chromosomes about one-third of normal
  at left end in duplication-bearing female and
  nearly normal to right of ct.
#
T(1;3)54a
 origin: X ray induced.
 discoverer: Lefevre, 54a4.
 synonym: T(1;3)w[+54a4].
 references: 1955, DIS 29: 73.
 genetics: A section of X chromosome including w[+], but
  not spl, inserted into chromosome 3.
#
T(1;3)54c
 origin: X ray induced.
 discoverer: Lefevre, 54c10.
 synonym: T(1;3)w[+54c10].
 references: 1955, DIS 29: 73.
 genetics: Section of X chromosome including w[+]
  inserted into chromosome 3.
#
T(1;3)65
 cytology: T(1;3)16-17;79D.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Male viable and sterile.
#
T(1;3)102
 origin: X ray induced.
 discoverer: Sturtevant, 1930.
 references: Dobzhansky, 1932, Biol. Zentr. 52: 495.
 genetics: Breakpoint in X chromosome between bb and
  centromere; break in 3L between ru and
  se. Crossing over in 3L greatly reduced.
  Male and homozygous female fertile. Male and female
  hyperploid for the 3L[D]X[P] element survive and
  are fertile; duplicated for locus of ru but not
  se, h, car, or bb.
#
T(1;3)107
 discoverer: Sturtevant, 1930.
 genetics: Probably a segment from chromosome 3 is
  intercalated into X chromosome since segregants
  are a Minute-bearing 3 [presumably
  Df(3)107] and a Minute-suppressing X
  [presumably Dp(3;1)107]. Male viable;
  homozygous female lethal.
#
T(1;3)143-3
 origin: X ray induced.
 discoverer: Neuhaus.
 synonym: T(1;3)Del143-3.
 references: 1941, DIS 15: 16.
 genetics: Two breaks in X chromosome, one between sc
  and br and another near the centromere. A break
  in chromosome 3 is between st and the
  centromere of 3. The y[+] and sc[+]
  loci are then attached to proximal end of 3L,
  and the distal end of 3L is attached to
  centromere of X. Bulk of the X chromosome
  is acentric and lost.
#
T(1;3)260-21
 cytology: T(1;3)6C;70E-F.
 origin: X ray induced simultaneously with In(1)y[260-21].
 discoverer: Sutton, 1939.
 references: 1943, Genetics 28: 210-17.
#
T(1;3)A1: Translocation (1;3) from Austin
 origin: X ray induced.
 discoverer: Muller, 1926.
 references: Painter and Muller, 1929, J. Heredity 20: 287-98.
 genetics: Breakpoints in X chromosome between dm and
  ec and between car and bb. Midsection
  of X translocated to 3R. Fly hyperploid for
  Dp(1;f)A1 survives; duplicated for loci of y
  through dm as well as bb (Schultz).
#
T(1;3)B[58l]: Translocation (1;3) Bar
 cytology: T(1;3)16A;88F.
 origin: X ray induced.
 discoverer: E. B. Lewis, 58l4.
 references: Ogaki, 1960, DIS 34: 97.
  1960, Japan J. Genet. 35: 282.
 genetics: Position effect at B. Male sterile.
#
T(1;3)B[S3i] Translocation (1;3) Bar-Super inserted in chromosome 3
 cytology: T(1;3)15F9-16A1;16A7-B1;19-20;Y;66B13-C1
   x ller; Lindsley); translocation between Dp(1;1)B
  = Dp(1;1)15F9-16A1;16A7-B1 and chromosome 3. X
  break can be shown genetically to separate f[+]
  from B and is assumed to separate the two
  halves of the Bar duplication.
 new order:: 1 - 16A1|20.Y[S];
  61 - 66B13|(16A1 - 19)|66C1 - 100.
  Tentative.
 origin: Neutron induced in X.Y[S], sc, w B.
 discoverer: Norby.
 references: Muller and Norby, 1949, DIS 23: 61.
 genetics: Associated with B[S3i]. Male viable.
  Homozygous female lethal. Chromosome 3
  containing inserted X material survives as
  duplication in presence of normal X chromosomes;
  male sterile; female fertile. Duplication has
  extreme B phenotype.
#
T(1;3)Bb: Translocation (1;3) Bubble
 cytology: T(1;3)13E;84F (Morgan, Bridges, and Schultz,
  1937, Carnegie Inst. Wash. Year Book 36: 301).
 origin: X ray induced.
 discoverer: R. L. King, 32d.
 genetics: Associated with Bb. Male sterile.
#
T(1;3)C48 Translocation (1;3) Crossover suppressor
 cytology: In(1)10E-F;18C-D; additional presence of
  T(1;3)20;80-81 inferred from genetic data.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Male lethal. Recombination reduced in X
  chromosome.
#
T(1;3)C151
 cytology: T(1;3)9D;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and sterile. Recombination reduced in
  X chromosome.
#
T(1;3)C152
 cytology: T(1;3)20;90E + Df(3R)88B-C;94A.
 new order:: 1 - 20|(90E - 88C|94A - 90E)|20;
  61 - 88B|94A - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male fertile. Recombination reduced in 3R.
#
T(1;3)C160
 cytology: T(1;3)14B;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male lethal. Recombination reduced in X
  chromosome.
#
T(1;3)C195
 cytology: T(1;3)11D;71A-B.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and sterile. Recombination reduced in
  X chromosome.
#
T(1;3)C250
 cytology: In(1)9F;15D-E; additional presence of
  T(1;3)20;80-81; inferred from genetic data.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and fertile; homozygous female viable.
  Recombination reduced in X chromosome.
#
T(1;3)C291
 cytology: T(1;3)16C;20;87F;98E.
 new order:: 1 - 16C|98E - 87F|(16C - 20)|87F
  - 61; 29|98B - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and fertile; homozygous female viable.
  Recombination reduced in 3R.
#
T(1;3)C300
 cytology: T(1;3)12C;61F;66E;68D.
 new order:: 1 - 12C|68D - 100;
  61 - 61F|66E - 61F|68D - 66E|12C - 20.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male dies in third larval instar. Recombination
  reduced in 3L.
#
T(1;3)C315
 cytology: T(1;3)20;70F.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male fertile; homozygous female lethal.
  Recombination reduced in 3L.
#
T(1;3)C329
 cytology: T(1;3)3F;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Male viable and sterile. Recombination reduced in
  X chromosome.
#
T(1;3)ct[11a]: Translocation (1;3) cut
 cytology: T(1;3)1B;7B2-3;8E-F;84B superimposed on
  R(1)1A3-4;19F-20A1.
 new order:: |1A4 - 1B|8E - 7B3|8F -
  20.20F - 20A1|;
  61 - 84B|(1B - 7B2)|84B - 100.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 1947.
 genetics: Mutant for ct but not y, ac, sc, cm, sn, or
  oc. Male lethal. Female carrying
  Dp(1;3)ct[11a] = Dp(1;3)1B;7B2-3;84B survives
  and has small eyes and arc-like wings with
  delta-like venation; duplicated for cm.
#
T(1;3)ct[12c1]
 cytology: T(1;3)7B2-3;7D2-6;85 superimposed on
  R(1)1A3-4;19F-20A1.
 new order:: |1A4 - 7B2|7D6 -
  20.20F - 20A1|;
  61 - 85|(7B3 - 7D2)|85 - 100.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 1947.
 genetics: Mutant for ct but not cm or sn. Male
  lethal. The derived Dp(1;3)ct[12c1] =
  Dp(1;3)7B2-3;7D2-6;85 survives as female and as
  sterile male; duplicated for sn.
#
T(1;3)ct[268-5]
 cytology: T(1;3)7B2-3;90C4-D1.
 origin: X ray induced.
 discoverer: Demerec, 33k.
 genetics: Mutant for ct but not scp or sn.
#
T(1;3)ct[268-21]
 cytology: T(1;3)7B3-4;7B4-5;96F.
 new order:: 1A - 7B3|96F - 61;
  20 - 7B5|96F - 100;
  deficient for 7B4.
 origin: X ray induced.
 discoverer: Hoover, 35i.
 genetics: Mutant for ct but not scp or sn. Male
  lethal.
#
T(1;3)ct[268-31]
 cytology: T(1;3)3D2-3;7B2-5;84D4-5;86B4-C1;88F (Hoover).
 new order:: 61 - 84D4|(3D3 - 7B2)|88F - 100;
  remainder not described.
 origin: X ray induced.
 discoverer: Demerec, 38d.
 genetics: Mutant for ct and dm but not scp, sn, or
  fa. Male lethal.
#
T(1;3)ct[268-36]
 cytology: T(1;3)7B2-C1;66F (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 39j.
 genetics: Mutant for ct. Male lethal.
#
T(1;3)ct[268-37]
 cytology: T(1;3)5D2-3;7B2-3;80C-F.
 new order:: 1 - 5D2|7B3 - 20;
  61 - 80C|7B2 - 5D3|80F - 100.
 origin: X ray induced.
 discoverer: Demerec, 39k.
 references: Sutton, 1940, Genetics 25: 534-40 (fig.).
  Demerec, 1940, Genetics 25: 618-27.
 genetics: Mutant for ct; variegated for rux and
  vs; shf, cm, and sn not affected. The
  segregant Dp(1;3)ct[268-37] =
  Dp(1;3)5D2-3;7B2-3;80C-F viable and fertile in both
  male and female. Its complement, Df(1)ct[268-37] =
  Df(1)5D2-3;7B2-3, survives as a Minute female;
  deficient for M(1)30, rux, vs, shf, and cm
  but not rg, cx, cv, or sn; mutant for
  ct.
#
T(1;3)cu[100.69]: Translocation (1;3) curled
 cytology: T(1;3)6B1-C1;88A4-B1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for cu.
#
T(1;3)D3
 cytology: T(1;3)4F;62A.
 origin: Induced by tritiated deoxycytidine.
 discoverer: Kaplan, 1965.
 references: 1966, DIS 41: 59.
 genetics: Male lethal.
#
T(1;3)f[257-29]: Translocation (1;3) forked
 cytology: T(1;3)15F5-16A1;64.
 origin: X ray induced.
 discoverer: Bishop, 40l.
 genetics: Mutant for f but not M(1)o, B, or os.
  Male viable and sterile.
#
T(1;3)fd: Translocation (1;3) furled
 cytology: T(1;3)7A;86E superimposed on In(3R)89C;96A
  (Darby).
 new order:: 1 - 7A|86E - 61;
  20 - 7A|86E - 89C|96A - 89C|96A - 100.
 origin: Induced by P[32] in In(3R)P.
 discoverer: Bateman, 1949.
 references: 1950, DIS 24: 54.
  1951, DIS 25: 77.
 genetics: Associated with fd.
#
T(1;3)H: Translocation (1;3) Hairless
 discoverer: Efroimson.
 references: Kamshilov, 1933, Biol. Zh. (Moscow) 2: 161-83.
 genetics: Break in X chromosome to the left of w;
  3R broken near H.
#
T(1;3)K2: Translocation (1;3) of Krivshenko
 cytology: T(1;3)20A-B;20D-F;80-81 superimposed on
  In(1)1B2-3;20B-D1. Inferred from genetic data
  since salivary chromosomes do not reveal an
  aberration. In ganglial metaphase,
  chromosome 3 is a rod-shaped and a J-shaped element.
 new order:: 1A - 1B2|20B|80 - 100;
  20F|80 - 61.
  Tentative.
 origin: X ray induced in In(1)sc[8].
 discoverer: Krivshenko, 55g3.
 references: 1956, DIS 30: 76.
 genetics: Irradiated In(1)sc[8] broken in distal region
  between y[+] and bb[+] and also near the
  centromere. Chromosome 3 broken near the
  centromere, whether to left or right of the
  centromere is not known. Tip of X chromosome
  with y[+] and ac[+] is attached to the
  chromosome 3 centromere, and one arm of this
  chromosome is attached to the X centromere.
  Bulk of the X chromosome is thus acentric and
  lost. Homozygote viable and moderately fertile.
  This chromosome may be considered as Dp(1;3)K2.
#
T(1;3)l-184: Translocation (1;3) lethal
 cytology: T(1;3)18A;81.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Associated with l(1)184.
#
T(1;3)l-v3: Translocation (1;3) lethal-variegated
 cytology: T(1;3)4A;81.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;3)l-v163
 cytology: T(1;3)17A-B;80-81; position of chromosome 3
  breakpoint with respect to centromere not determined.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;3)l-v252
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;3)l-v361
 cytology: T(1;3)19-20;80-81; positions of breakpoints
  with respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;3)l-v453
 cytology: T(1;3)12D;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;3)l-v455
 cytology: T(1;3)3C;81.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for w and a lethal. Male sterile.
#
T(1;3)l-v463
 cytology: T(1;3)19-20;81-82; positions of breakpoints
  with respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;3)lz[268-29]: Translocation (1;3) lozenge
 cytology: T(1;3)8D8-9;81F.
 origin: X ray induced.
 discoverer: Hoover, 38d.
 genetics: Mutant for lz and independently for ct but
  not sn, t, dvr, flp, or ras.
  T(1;3)lz[268-29]/lz female fertile. Male lethal.
#
T(1;3)N[34b]: Translocation (1;3) Notch
 origin: X ray induced.
 discoverer: Oliver, 34b3.
 references: 1937, DIS 7: 19.
 genetics: Carries mutant allele of N and normal alleles of
  w and ec.
 genetics: Reported as suspected of being a T(1;3); basis
  of suspicion not given.
#
T(1;3)N[50k11]
 cytology: T(1;3)1E3-4;3C6-7;3C8-9;89A; 3C7-8 missing
  (Lefevre).
 new order:: 1A1 - 1E3|3C9 - 20;
  61 - 89A|(1E4 - 3C6)|89A - 100.
 origin: X ray induced.
 discoverer: Lefevre, 50k11.
 references: 1951, DIS 25: 71.
  1952, DIS 26: 66.
  Ratty, 1954, Genetics 39: 513-28.
 genetics: Mutant for N. The segregant Dp(1;3)N[50k11] =
  Dp(1;3)1E3-4;3C6-7;8A is viable and carries normal
  alleles of pn, w, and rst.
#
T(1;3)N[264-6]
 cytology: T(1;3)3C9-D1;62A;73E;80C (Schultz).
 new order:: 1 - 3C9|80C - 73E|3D1 - 20;
  61 - 62A|73E - 62A|80C - 100.
 origin: X ray induced.
 discoverer: Demerec, 33k20.
 genetics: Variegates for w and N; position effect on
  pb and Dfd. X/Y male lethal; X/Y/Y
  viable and sterile. Dp(3;1)N[264-6] =
  Dp(3;1)3C9-D1;73E;80C viable. Df(3L)N[264-6] =
  Df(3L)73E;80C survives and is Minute, possibly
  deficient for M(3)S34.
#
T(1;3)N[264-29]
 cytology: T(1;3)3D4-5;80 (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 36d.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Variegates for rst, fa, and dm but not w
  or ec. X/Y male lethal; X/Y/Y occasionally
  survives.
#
T(1;3)N[264-34]
 cytology: T(1;3)3C3-5;70C2-3 (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 37a.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Contains mutant allele of N and normal alleles of
  w, rst, and dm.
#
T(1;3)N[264-55]
 cytology: T(1;3)3D4-5;80F9-81F1; chromosome 3
  claimed broken in 3R.
 origin: X ray induced.
 discoverer: Demerec, 38b.
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
 genetics: Variegates for w, rst, fa, and dm but not
  pn, kz, or ec.
#
T(1;3)N[264-56]
 cytology: T(1;3)3D4-5;80 (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 38c.
 genetics: Variegates for w and probably N.
#
T(1;3)N[264-58]
 cytology: T(1;3)3B2-3;3D6-7;80D-F (Sutton).
 new order:: 1 - 3B2|3D7 - 20;
  61 - 80D|3D6 - 3B3|80F - 100.
 origin: X ray induced.
 discoverer: Demerec, 38d.
 synonym: T(1;3)w[m264-58].
 references: 1940, Genetics 25: 618-27.
  Sutton, 1940, Genetics 25: 534-40 (fig.).
 genetics: Variegates for w, rst, N, and its pseudoalleles
  (Cohen, 1962, Genetics 47: 647-59); seems to carry
  a mutant allele of dm. The segregant
  Df(1)N[264-58] = Df(1)3B2-3;3D6-7 survives in
  heterozygous female and is deficient for w, rst,
  fa, and dm but not pn or ec.
  Dp(1;3)N[264-58] = Dp(1;3)3B2-3;3D6-7;80D-F
  survives as both male and female.
#
T(1;3)N[264-64]
 cytology: T(1;3)3E5-6;80C-F (Hoover).
 origin: X ray induced.
 discoverer: Demerec, 38e.
 references: 1941, Proc. Intern. Congr. Genet., 7th.,
  pp. 99-103.
 genetics: Variegates for w, rst, fa, and dm but not
  pn, kz, or ec.
#
T(1;3)N[264-65]
 cytology: T(1;3)2B10-16;3D4-5;81F;96C4-5 (Hoover).
 new order:: 1 - 2B10|(81F - 96C4)|3D5 - 20;
  61 - 81F|(2B16 - 3D4)|96C5 - 100.
 origin: X ray induced.
 discoverer: Demerec, 38e.
 genetics: Variegates for w, rst, fa, and dm but not
  kz.
#
T(1;3)n[264-70]
 cytology: T(1;3)3C4-5;80D-F + T(1;3)6F2-7A1;100B2-3
  (Sutton).
 new order:: 1 - 3C4|80F - 100B2|6F2 - 3C5|80D
  - 61;
  20 - 7A1|100B3 - 100F.
 origin: X ray induced.
 discoverer: Demerec, 38k.
 references: Sutton, 1940, Genetics 25: 534-40.
 genetics: Variegates for w, rst, fa, and dm but not
  kz, pn, ec, cm, scp, or shf.
#
T(1;3)N[264-83]
 cytology: T(1;3)3C6-7;12F2-4;79E2-3 + In(3R)81;88
  (Sutton).
 new order:: 1 - 3C6|12F2 - 3C7|79E3 - 81|88
  - 81|88 - 100;
  20 - 12F3|79E2 - 61.
 origin: X ray induced.
 discoverer: Demerec, 39d.
 references: 1941, Proc. Intern. Congr. Genet., 7th.,
  pp. 99-103.
 genetics: Carries mutant allele of N and normal alleles of
  w, rst, and dm.
#
T(1;3)N[264-100]
 cytology: T(1;3)3B4-C1;4B4-5;80 [Sutton, 1940, Genetics
  25: 534-40 (fig.); Gersh, 1959, Genetics 44: 163-72].
 new order:: 1 - 3B4|4B5 - 20;
  61 - 80|4B4 - 3C1|80 - 100.
 origin: X ray induced.
 discoverer: Demerec, 39l.
 references: 1940, Genetics 25: 618-27.
 genetics: Variegates for w, rst, fa, dm, and ec but not
  pn or bi. The segregant Df(1)N[264-100]
  = Df(1)3B4-C1;4B4-5, which is deficient for N and
  M(1)3E, survives in heterozygous female.
  Dp(1;3)N[264-100] = Dp(1;3)3B4-C1;4B4-5;80
  originally survived in female but not male; more
  recently, male carrying duplication found to survive
  (Gersh, 1959).
#
T(1;3)N[264-104]
 cytology: T(1;3)3C7-9;87D1-E1 + In(1)1B4-5;18-19 (Sutton).
 new order:: 1A1 - 1B4|18 - 3C9|87D1 - 61;
  20 - 19|1B5 - 3C7|87E1 - 100.
 origin: X ray induced.
 discoverer: Demerec, 39j.
 genetics: Mutant for svr and N but not ac, sc, sta,
  tw, w, rst, p, ss, k, or e.
#
T(1;3)N[264-121]
 cytology: T(1;3)3C7-9;81F;86B6-C1 (Sutton).
 new order:: 1 - 3C7|81F - 86B6|81F - 61;
  20 - 3C9|86C1 - 100.
 origin: X ray induced.
 discoverer: Demerec, 40j.
 genetics: Carries muant allele of N and normal alleles of
  kz, w, and dm.
#
T(1;3)O4: Translocation (1;3) of Oliver
 origin: X ray induced.
 discoverer: Oliver, 29k24.
 references: Dobzhansky and Schultz, 1934, J. Genet. 280: 373-77.
  Oliver, 1937, DIS 7: 19.
 genetics: X chromosome broken between m and g and
  between f and car. Center section of X
  then inserted into 3L. The segregant
  Df(1)O4 is inviable when added to a normal male genotype,
  poorly viable when added to a normal female
  genotype, and survives well when added to an
  intersex (2X:3A) genotype where it confers a
  low degree of fertility. The reciprocal segregant,
  Dp(1;3)O4, is lethal in the male, survives well
  in the female, and poorly in the intersexes.
#
T(1;3)O5
 cytology: T(1;3)4F2-3;62B-C;88A-C;92C-D (Lewis, 1951, DIS
  25: 108-9).
 new order:: 1 - 4F2|88C - 92C|4F3 - 20;
  61 - 62B|88A - 62B|92D - 100.
 origin: X ray induced.
 discoverer: Oliver, 29l30.
 references: 1937, Am. Naturalist 71: 560-66.
  1938, Genetics 23: 162.
 genetics: Male viable and fertile. Homozygous female viable and
  sterile. The segregant Dp(3;1)O5 =
  Dp(3;1)4F2-3;88A-C;92C-D is viable and fertile in
  male and female. It is duplicated for loci of
  red, jvl, cv-c, su(Hw), sbd, ss, bx, sr, gl, k,
  and Dl but not cu, ry, kar, or e (Lindsley
  and Grell, 1958, DIS 32: 136; E. B. Lewis).
  Produces roughish eyes, spread and nicked wings, coarse
  bristles, and a darkly-pigmented abdomen.
#
T(1;3)O6
 origin: X ray induced.
 discoverer: Oliver, 34d24.
 genetics: Mutant for ec. Break in 3L between ru
  and h. Break in X not determined. Male and
  homozygous female viable and fertile.
#
T(1;3)OR1: Translocation (1;3) from Oak Ridge
 cytology: T(1;3)5A;20;66B;79E.
 new order:: 1 - 5A|79E - 66B|5A - 20|79E - 100;
  20|66B - 61.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal. Male hyperploid for 3L[D]X[P]
  element survives.
#
T(1;3)OR6
 cytology: T(1;3)4D;87F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR7
 cytology: T(1;3)14D;91E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR9
 cytology: T(1;3)6D;66B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Variegated for a lethal; male sterile. Male has small,
  rough eyes; perhaps mutant for rux.
#
T(1;3)OR11
 cytology: T(1;3)18F;84B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR12
 cytology: T(1;3)2B6-13;84A + T(1;3)18D;98F-99A (Becker).
 new order:: 1 - 2B6|84A - 98F|18D - 2B13|84A - 61;
  20 - 18D|99A - 100.
  Tentative.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3R[P]X[D] element survives.
#
T(1;3)OR13
 cytology: T(1;3)15A;84E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR14
 cytology: T(1;3)17A;80B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Variegated for a lethal; male sterile.
#
T(1;3)OR15
 cytology: T(1;3)18D;88A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Subsequently acquired a
  male lethal.
#
T(1;3)OR17
 cytology: T(1;3)19E;67C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile. Homozygous female viable.
  Male hyperploid for 3L[D]X[P] survives.
#
T(1;3)OR18
 cytology: T(1;3)19B;80A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR19
 cytology: T(1;3)12E;75F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR21
 cytology: T(1;3)19E;61F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile; X/0 male dies. Male
  hyperploid for 3L[D]X[P] element survives.
#
T(1;3)OR22
 cytology: T(1;3)6C;98C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile. Homozygous female viable.
#
T(1;3)OR23
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR24
 cytology: T(1;3)12F;80B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR25
 cytology: T(13)20B;99B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3R[D]X[P] element survives.
#
T(1;3)OR28
 cytology: T(1;3)11A;80C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;3)OR29
 cytology: T(1;3)16F;84B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR30
 cytology: T(1;3)19E;65D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3L[D]X[P] element survives.
#
T(1;3)OR31
 cytology: T(1;3)10A;68D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR32
 cytology: T(1;3)16A;71B.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR33
 cytology: T(1;3)13E;62F.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male virtually lethal.
#
T(1;3)OR34
 cytology: T(1;3)3A;65A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile, has either a normal
  Y or B[S]w[+]Y.
#
T(1;3)OR35
 cytology: T(1;3)19E;75C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR36
 cytology: T(1;3)7D;62A;87E.
 new order:: 1 - 7D|62A - 87E|62A - 61;
  20 - 7D|87E - 100.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR37
 cytology: T(1;3)3C;97F.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile; homozygous female viable.
#
T(1;3)OR38
 cytology: T(1;3)18D;61D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3L[D]X[P] survives.
#
T(1;3)OR39
 cytology: T(1;3)6B-F;75C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR40
 cytology: T(1;3)6F;62D + T(1;3)16B;20;84F.
 new order:: 1 - 6F|62D - 84F|20 - 16B |84F - 100;
  20|16B - 6F|62D - 61.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR41
 cytology: T(1;3)9F;98E.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR43
 cytology: T(1;3)20A;97D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3R[D]X[P] element survives.
#
T(1;3)OR45
 cytology: T(1;3)17A;61D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR46
 cytology: T(1;3)12C;80A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Variegated for a lethal; male sterile.
#
T(1;3)OR47
 cytology: T(1;3)20;93D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and fertile; homozygous female viable.
  Male hyperploid for 3R[D]X[P] element survives.
#
T(1;3)OR49
 cytology: T(1;3)11A;66D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR51
 cytology: T(1;3)12D;97A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;3)OR52
 cytology: T(1;3)19E;70C;83F.
 new order:: 1 - 19E|83F - 70C|83F - 100;
  20 - 19E|70C - 61.
  Tentative.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR54
 cytology: T(1;3)12F;83A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;3)OR55
 cytology: T(1;3)11C;67C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR57
 cytology: T(1;3)3E;5B;61C.
 new order:: 1 - 3E|5B - 3E|61C - 100;
  20 - 5B|61C - 61A.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male lethal. Lethality not covered by
  B[S]w[+]Y;
  therefore, probably associated with break in 5B.
#
T(1;3)OR59
 cytology: T(1;3)20;80-81; positions of breakpoints with respect
  to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;3)OR60
 cytology: T(1;3)4B;88A.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male lethal.
#
T(1;3)OR62.
 cytology: T(1;3)10F;88C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR63
 cytology: T(1;3)20;80-81; positions of breakpoints with respect
  to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male sterile.
#
T(1;3)OR66
 cytology: T(1;3)3F;71E.
 origin: X ray induced in y.
 discoverer: Warters, 1961.
 genetics: Male lethal; lethality not covered by B[S]w[+]Y.
#
T(1;3)OR67
 cytology: T(1;3)4C;73C.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR69
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR71
 cytology: T(1;3)20;71D.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Male viable and sterile.
#
T(1;3)OR72
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: X ray induced.
 discoverer: Warters, 1961.
 genetics: Variegated for a lethal. Male sterile.
#
T(1;3)os[bdw] Translocation (1;3) outstretched small eye-bending wings
 cytology: T(1;3)16E;80C (Nicoletti).
 origin: X ray induced.
 discoverer: Halfer, 1960.
 genetics: Associated with os[bdw]. Male sterile.
#
T(1;3)P104: Translocation (1;3) from Pasadena
 cytology: T(1;3)19-20;87F-88A.
 origin: X ray induced.
 discoverer: E. B. Lewis.
#
T(1;3)ras[v] Translocation (1;3) raspberry-variegated
 cytology: T(1;3)9E;13C;81F (E. B. Lewis).
 new order:: 1 - 9E|13C - 20;
  61 - 81F|(9E - 13C)|81F - 100.
 origin: Fast neutron induced.
 discoverer: E. B. Lewis, 1953.
 references: Brokaw, 1954, DIS 28: 73.
 genetics: Shows recessive variegation for ras and a rough
  eye and dominant variegation for a wing effect
  resembling Bg/+. No variegation for m, vb,
  sd, sl, or un. Is probably an enhancer of
  B; a few ras[v]/ras[v] females somewhat
  resemble B/+. Dp(1;3)ras[v] = Dp(1;3)9E;13C;81F
  male dies but female survives; duplicated for ras,
  v, m, dy, and g but not un or r.
  Df(1)ras[v] is lethal in both sexes.
#
T(1;3)rst: Translocation (1;3) roughest
 origin: X ray induced.
 discoverer: Ball, 32b25.
 genetics: Associated with rst. Breakpoints in X
  chromosome near w and bb; position of
  breakpoint in chromosome 3 unknown.
#
T(1;3)ry[35]: Translocation (1;3) rosy
 cytology: T(1;3)20;87C-E;91B-C (Lindsley).
 new order:: 1 - 20|(87E - 91B)|20;
  61 - 87C|91C - 100.
 origin: X ray induced in cu kar chromosome.
 discoverer: Schalet.
 references: 1964, DIS 39: 62-64.
  Schalet, Kernaghan, and Chovnick, 1964, Genetics
  50: 1261-68.
 genetics: Deficient, mutant, or variegated for ry and
  pic. The segregant, Dp(3;1)ry[35] =
  Dp(3;1)20;87C-E;91B-C is viable and fertile in
  male and female; duplicated for loci of Sb and
  Ubx
#
T(1;3)sc[260-15]: Translocation (1;3) scute
 cytology: T(1;3)1B4-5;71C-D.
 origin: X ray induced.
 discoverer: Demerec, 38l.
 references: Sutton, 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y or ac. Male
  sterile.
#
T(1;3)sc[260-20]
 cytology: T(1;3)1A8-B1;61A1-2.
 origin: X ray induced.
 discoverer: Sutton, 39e.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for sc but not y, ac, or svr.
  Male and homozygous female viable and fertile. The
  two halves of the translocation are recoverable
  independently. The 3L[D]X[P] element should be
  deficient for y and ac but carry
  sc[260-20]; it presumably is male lethal but
  survives in heterozygous female. The X[D]3[P]
  element carries normal alleles of y and ac
  but not sc[260-20] or svr[+] and
  should also carry normal alleles of ve and ru.
#
T(1;3)sc[J4] Translocation (1;3) scute of Jacobs-Muller
 cytology: T(1;3)1B;3A3-C2;61A (inferred from genetic
  tests); 1B-3A3 lost.
 new order:: 1A1 - 1B|61A - 100;
  20 - 3C2|61A.
 origin: X ray induced.
 discoverer: Jacobs-Muller.
 references: Muller, 1932, Proc. Intern. Congr. Genet., 6th.,
  Vol. 1: 225.
  1934, DIS 2: 60.
 genetics: The section of the X chromosome from 1B through
  3A was presumably inserted elsewhere in the genome;
  it subsequently separated from the rest of the
  configuration and was lost. Base of the X,
  presumably capped by the indemonstrable terminus
  of 3L (i.e., 3[D]X[P]), is deficient for
  the tip of X through z and may be stocked in
  combination with a duplication for the tip of X,
  such as the X[D]4[P] element from
  T(1;4)w[m5] or Dp(1;f)z[9].
  The X[D]3[P]
  segregant carries normal alleles of l(1)J1, y,
  and ac but is not demonstrably deficient for
  3L factors since it is homozygous viable.
  y[+] localizes about 4 units to the left of
  ru.
#
T(1;3)sc[K] Translocation (1;3) scute of Krivshenko
 discoverer: Krivshenko.
 references: Agol, 1936, DIS 5: 7.
 genetics: Mutant for sc. Three-break rearrangement with
  X[D] translocated to 3L[P];
  3L[D]
  translocated to 3R[P] and 3R[D] translocated
  to X[P].
#
T(1;3)sc[K3]
 cytology: T(1;3)1B2-3;61A1-2.
 origin: X ray induced.
 discoverer: Krivshenko, 53j29.
 references: 1959, DIS 33: 95-96.
 genetics: Mutant for sc. Male fertile. Two halves of the
  translocation recoverable separately. X[D]3[P]
  element is viable homozygous, although males are
  somewhat infrequent. 3[D]X[P] is inviable in
  male and homozygous female but survives in
  heterozygous female.
#
T(1;3)sn[13a1]: Translocation (1;3) singed
 cytology: T(1;3)6C;7C9-10;79D2-E1; chromosome 3. X
  material inserted into chromosome 3.
 new order:: |1A4 - 6C|7C10 -
  20.20F - 20A1|;
  61 - 79D2|(6C - 7C9)|79E1 - 100.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 1947.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Mutant for sn. The segregant Dp(1;3)sn[13a1] =
  Dp(1;3)6C;7C9-D1 survives and is duplicated for
  cm and ct.
#
T(1;3)sn[19Bb5]
 cytology: T(1;3)3C1-2;7C9-10;72A-B superimposed on
  In(1)1B3-4;20B-D1[L]1B2-3;20B-D1[R] +
  In(1)4D7-E1;11F2-4.
 new order:: 1A - 1B3|20B - 11F4|4E1 - 7C9|3C1
  - 1B3|20D1 - 20F;
  61 - 72A|(3C2 -
  4D7|11F2 - 7C10)|72B - 100.
 origin: X ray induced in In(1)sc[S1L]sc[8R]+dl-49.
 discoverer: Muller, Valencia, and Valencia, 1946-53.
 references: Valencia, 1966, DIS 41: 58.
 genetics: Associated with sn[19Bb5]. w not affected.
  T(1;3)SP2: Translocation (1;3) from Sao Paulo T(1;3)SP2: Translocation (1;3) from So'~a'o Pauloc
 cytology: T(1;3)20;90E.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP11
 cytology: T(1;3)20;75B.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP13
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP14
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP15
 cytology: T(1;3)20;67.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3L[D]X[P] element survives.
#
T(1;3)SP21
 cytology: T(1;3)1B;83F.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP22
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP26
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP34
 cytology: T(1;3)8A;84A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP37
 cytology: T(1;3)8F;64E.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP38
 cytology: T(1;3)10;84.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP41
 cytology: T(1;3)3E;67C-D.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP44
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP46
 cytology: T(1;3)11;98.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP53
 cytology: T(1;3)12;92.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP54
 cytology: T(1;3)20;67B.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3L[D]X[P] element survives.
#
T(1;3)SP59
 cytology: T(1;3)20;83C.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP62
 cytology: T(1;3)20;89A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP63
 cytology: T(1;3)20;65.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for the
  3L[D]X[P] element survives.
#
T(1;3)SP68
 cytology: T(1;3)11A;80-81.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP70
 cytology: T(1;3)20;80-81; positions of breakpoints with
  respect to centromeres not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP73
 cytology: T(1;3)20;89E.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Mutant for Ubx. Male viable and sterile.
#
T(1;3)SP79
 cytology: T(1;3)13D;64A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP80
 cytology: T(1;3)18C;100A.
 origin: Gamma ray induced in y w.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile. Male hyperploid for
  3R[D]X[P] element survives.
#
T(1;3)SP82
 cytology: T(1;3)5B-C;81.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP85
 cytology: T(1;3)16B;80-81; position of chromosome 3
  breakpoint with respect to centromere not determined.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP90
 cytology: T(1;3)18D;68A.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP99
 cytology: T(1;3)12E;64E.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP112
 cytology: T(1;3)11B;85D.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)SP122
 cytology: T(1;3)11E;92E.
 origin: Gamma ray induced.
 discoverer: Lindsley and Musatti, 1961.
 genetics: Male viable and sterile.
#
T(1;3)ss[v] Translocation (1;3) spineless-variegated
 cytology: T(1;3)20;89B;100F; breakpoint in X
  chromosome inferred from genetic results; not
  visible cytologically.
 new order:: 1 - 20|(89B - 100F)|20;
  61 - 89B|100F.
  Tentative.
 origin: X ray induced.
 discoverer: E. B. Lewis.
 genetics: Variegated for ss and mutant for aristapedia.
  Male viable and sterile.
#
T(1;3)sta: Translocation (1;3) stubarista
 cytology: T(1;3)1D3-E1;2A;89B21-C4 (E. B. Lewis).
 new order:: 1A - 1D3|2A - 20;
  61 - 89B21|(1E1
  - 2A)|89C4 - 100.
 origin: X ray induced.
 discoverer: Oliver, 32l22.
 references: 1935, DIS 4: 15.
 genetics: Mutant for sta and ss[a]. Male viable and
  fertile; homozygous female lethal. The segregant
  Dp(1;3)sta = Dp(1;3)1D3-E1;2A;89B21-C4 is
  viable. The complementary Df(1)sta =
  Df(1)1D3-E1;2A is viable in heterozygous female
  either as Df(1)sta/+; +/+ or as
  Df(1)sta/Df(1)sta; Dp(1;3)sta/+ with the second type being
  sterile.
#
T(1;3)Th1: Translocation (1;3) from Thymidine
 cytology: T(1;3)12C;65B.
 origin: From male treated with H[3]-thymidine as larva.
 discoverer: Kaplan.
 genetics: Male lethal.
#
T(1;3)v: Translocation (1;3) vermilion
 cytology: T(1;3)10;93B (Lewis, 1951, DIS 25: 108-9).
 origin: X ray induced in a chromosome carrying v.
 discoverer: E. G. Anderson, 1924.
 references: 1925, Papers Mich. Acad. Sci. 5: 355-66.
  1926, Papers Mich. Acad. Sci. 7: 273-78.
  1929, Z. Induktive Abstammungs- Vererbungslehre
  51: 397-411.
 genetics: Inseparable from v. Male viable and sterile.
  Primary nondisjunction occurs with a frequency of
  about 2% in heterozygous females, secondary
  nondisjunction is 23%. Crossing over is reduced
  near v but approaches normal on both ends of the
  X.
#
T(1;3)Vel: Translocation (1;3) Velvet
 origin: X ray induced in In(1)sc[8].
 discoverer: Patterson.
 references: 1934, DIS 2: 10.
 genetics: Associated with Vel. Homozygous viable and
  fertile.
#
T(1;3)w[m1]: Translocation (1;3) white-mottled
 origin: X ray induced.
 discoverer: Muller, 1927.
 references: 1930, J. Genet. 22: 299-334.
 genetics: Variegated for w and N. X/Y lethal;
  X/Y/Y viable and sterile.
 genetics: First recorded case of variegated position effect.
#
T(1;3)w[m2]
 origin: X ray induced.
 discoverer: Patterson.
 references: Muller, 1930, J. Genet. 22: 299-334.
 genetics: Variegated for w. Male sterile.
#
T(1;3)w[m49a]
 cytology: T(1;3)3A10-B1;3E2-3;80.
 new order:: 1 - 3A10|3E3 - 20;
  61 - 80|(3B1 - 3E2)|80 - 100.
 origin: X ray induced.
 discoverer: Lefevre, 49a7.
 synonym: T(1;3)w[mSp]: Translocation (1;3) white-mottled Spotted.
 references: 1949, DIS 23: 59.
  1951, DIS 25: 71.
  Ratty, 1954, Genetics 39: 513-28.
 genetics: Variegated for w, rst, and spl. The two
  elements of the translocation can be separated;
  Df(1)w[m49a] = Df(1)3A10-B1;3E2-3 survives in
  heterozygous female and is N; Dp(1;3)w[m49a]
  = Dp(1;3)3A10-B1;3E2-3;80 survives in both male and
  female and carries the loci of w, rst, N, and
  (from the cytology) presumably dm.
#
T(1;3)w[m258-32]
 cytology: T(1;3)3C3-5;81 (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 37l.
 genetics: Variegated for w but not rst, fa, or dm.
  Male viable.
#
T(1;3)w[m258-44]
 cytology: T(1;3)3C3-4;4D2-E1;80D; deficient for 3C4-4D2.
 origin: Aneuploid segregant from T(1;2;3)w[m258-44]/+.
#
T(1;3)w[m258-54]
 cytology: T(1;3)3B2-C1;19F2-20A1;20E;63C7-8.
 new order:: 1 - 3B2|63C8 - 100;
  20F|19F2 - 3C1|20A1 - 20E|63C7 - 61.
 origin: X ray induced.
 discoverer: Sutton, 40e.
 genetics: Variegated for w and rst but not pn
  or spl. Male lethal.
#
T(1;3)w[m609e]
 cytology: T(1;3)3C2-3;100C3-4.
 origin: X ray induced.
 discoverer: Patterson.
 synonym: T(1;3)Aw[m609e].
 references: Griffen and Stone, 1938, Genetics 23: 149.
 genetics: Variegated for w. Seems likely that the
  rearrangement is more complicated because a
  euchromatic-euchromatic translocation would not be
  expected to produce variegation.
#
T(1;3)w[vco]: Translocation (1;3) white-variegated cobbled
 cytology: T(1;3)2B17-C1;3C4-5;77D3-5;81 (Schultz).
 new order:: 1A - 2B17|3C5 - 20;
  61 - 77D3|2C1 - 3C4|81 - 77D5|81 - 100.
 discoverer: Clausen.
 genetics: Variegated for w and rst and apparently
  mutant for in but eg, Dfd, Dfd[r], pb, and
  p not affected. in effect probably
  associated with 77D3-5 break. Each element of the
  translocation survives as an aneuploid.
  Df(1)w[vco] = Df(1)2B17-C1;3C4-5 is deficient
  for recessives from kz through the dwarf
  character of rst[2] (i.e., rst but not
  vt). Df(1)w[vco]/T(1;3)w[vco] is w,
  extreme rst, and highly infertile.
  Dp(1;3)w[vco] = Dp(1;3)2B17-C1;3C4-5;77D3-5;81
  covers w and rst.
#
T(1;3)y[260-11]: Translocation (1;3) yellow
 cytology: T(1;3)1B2-3;85F1-5.
 origin: X ray induced.
 discoverer: Sutton, 39a.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for y but not ac, sc, or svr.
  Male viable and sterile.
#
T(1;3)y[260-21]
 cytology: T(1;3)6C;70E-F + In(1)1A6-7;5D8-E1.
 new order:: 1A1 - 1A6|5D8 - 1A7|5E1 - 6C|70F
  - 100;
  20 - 6C|70E - 61.
 origin: X ray induced.
 discoverer: Sutton, 1939.
 references: 1943, Genetics 28: 210-17.
 genetics: Mutant for y but not sc. Male lethal.
#
T(1;3;4)A: Translocation (1;3;4) from Austin
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 synonym: T(1;4)3A.
 references: Painter and Stone, 1935, Genetics 20: 327-41.
#
T(1;3;4)A96b
 discoverer: T(1;3;4)3C3-7;10;101F; break in
  chromosome 3 not determined (Mackenson, 1935).
 new order:: 1 - 3C3|3[P];
  20 - 3C7|101F - 102F;
  3[D]|101F - 101A.
 origin: X ray induced.
 discoverer: Mackensen.
 references: 1935, J. Heredity 26: 163-74 (fig.).
 genetics: Variegated for w.
#
T(1;4)231b
 origin: X ray induced.
 discoverer: Patterson.
 references: Patterson and Painter, 1931, Science 73: 530-31.
  Patterson, 1932, Am. Naturalist 66: 193-206.
  1932, Genetics 17: 38-59.
 genetics: Variegated for N and w. Left end of X
  from sc to ec attached to chromosome 4.
#
T(1;4)A1: Translocation (1;4) from Austin
 cytology: T(1;4)9B;20;101-102.
 new order:: 1 - 9B|20;
  101|9B - 20|102.
 origin: X ray induced.
 discoverer: Muller, 1928.
 synonym: CRB; W13; T(1;4)w[13]; T(1;4)1.
 references: Muller and Stone, 1930, Anat. Record 47: 393-94.
  Muller and Painter, 1932, Z. Induktive Abstammungs-
  Vererbungslehre 62: 316-65.
  Painter, 1934, Genetics 19: 448-69.
 genetics: X chromosome broken between lz and ras
  and between bb and the centromere. The
  segregant, Dp(1;4)A1 = Dp(1;4)9B;20;101-102, is
  lethal when added to a normal male genotype, causing
  failure of separation of the germ layers (Poulson,
  1940, J. Exptl. Zool. 83: 271-325). Segregant
  added to a normal female or triploid intersex
  genotype produces females with low fertility
  (Pipkin, 1940, Texas Univ. Publ. 4032: 126-56).
  The reciprocal, Df(1)A1 = Df(1)9B;20, causes
  death associated with incomplete blastoderm
  formation when added to male genotype (Poulson,
  1940); it results in poorly fertile females when
  added to normal female or triploid intersex
  genotypes (Pipkin, 1940).
#
T(1;4)A2
 cytology: Chromosome 4 appended to X as second arm.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: Painter and Stone, 1935, Genetics 20: 327-41
  (fig.).
 genetics: Translocation involves short arm of one and base of
  long arm of the other. Unlike most X-4
  pseudofusions, crossing over between f and the
  centromere is virtually eliminated.
#
T(1;4)A3
 cytology: About 10% of metaphase length of X chromosome
  transferred to chromosome 4.
 origin: X ray induced.
 discoverer: Patterson, 30l.
 synonym: T(1;4)w[m3].
 references: Patterson and Painter, 1931, Science 73: 530-31.
  Patterson, 1932, Genetics 17: 38-59.
  Muller and Painter, 1932, Z. Induktive Abstammungs-
  Vererbunglehre 62: 316-65.
 genetics: Variegated for w and N. X broken between
  w and ec.
#
T(1;4)A4
 cytology: T(1;4)13F6-14A1-102F [inferred from
  figs. 17D, E, and F of Mackensen (1935) and Texas
  Univ. Publ. 4032: frontispiece (1940)].
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: 1934, Am. Naturalist 68: 359-69.
  Stone, 1934, Genetica 16: 506-20.
  Mackensen, 1935, J. Heredity 26: 163-74 (fig.).
  Patterson, Stone, and Bedichek, 1935, Genetics
  20: 259-79 (fig.).
  1937, Genetics 2: 407-26.
  Pipkin, 1940, Texas Univ. Publ. 4032: 126-56.
 genetics: X chromosome broken between sd and f.
  Homozygous viable and fertile. Both the
  4[D]X[P] and the reciprocal X[D]4[P]
  elements survive when added to diploid female or
  intersex genotypes. X/X/4[D]X[P] females, but not
  the other genotypes, are fertile.
#
T(1;4)A5
 cytology: Chromosome 4 appended to X as second arm.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: Stone, 1934, Genetica 16: 506-20.
  Painter and Stone, 1935, Genetics 20: 327-41
  (fig.).
 genetics: Translocation involves short arm of one chromosome
  and base of long arm of the other. Crossing over at
  base of X normal.
#
T(1;4)A6
 cytology: Chromosome 4 appended to X as second arm.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: Stone, 1934, Genetica 16: 506-20.
  Painter and Stone, 1935, Genetics 20: 327-41 (fig.).
 genetics: Same as T(1;4)A5.
#
T(1;4)A7
 cytology: Chromosome 4 appended to X as second arm.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: Stone, 1934, Genetica 16: 506-20.
  Painter and Stone, 1935, Genetics 20: 327-41 (fig.).
 genetics: Same as T(1;4)A5.
#
T(1;4)A8
 cytology: T(1;4)11A6-7 (1940, Texas Univ. Publ. 4032: frontispiece);
  breakpoint in chromosome 4 unknown.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: 1934, Am. Naturalist 68: 359-69.
  Stone, 1934, Genetica 16: 506-20.
  Patterson, Stone, Bedichek, 1935, Genetics 20: 259-79 (fig.).
  1937, Genetics 22: 407-26.
  Pipkin, 1940, Texas Univ. Publ. 4032: 126-56.
 genetics: X chromosome broken between fw and wy and
  chromosome 4 to the left of bt. Homozygous
  viable and fertile. Both the X[D]4[P] and the
  4[D]X[P] elements added to a normal diploid
  female genotype produce weakly fertile hyperploid
  females and when added to a triploid intersec
  genotype, produce sterile hypoploid triploid females.
#
T(1;4)A9
 cytology: T(1;4)5A1-4 (1940, Texas Univ. Publ. 4032: frontispiece).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: 1934, Am. Naturalist 68: 359-69.
  Stone, 1934, Genetica 16: 506-20.
  Patterson, Stone, and Bedichek, 1935, Genetics 20: 259-79.
  1937, Genetics 22: 407-26.
  Pipkin, 1940, Texas Univ. Publ. 4032: 126-56.
 genetics: X chromosome broken between rg and cv;
  chromosome 4 broken to the left of bt. Homozygous
  viable and fertile. The X[D]4[P] element added
  to a normal diploid female genotype produces
  partially fertile hyperloid females; it survives when
  added to a triploid intersex genotype. Its
  complement, 4[D]X[P], is virtually lethal when
  added to a diploid female but produces a partially
  fertile hypotriploid when added to triploid intersex
  genotype.
#
T(1;4)A10
 cytology: T(1;4)1A5-6;102A2-4.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: 1934, Am. Naturalist 68: 359-69.
  Stone, 1934, Genetica 16: 506-20.
  Stone and Griffen, 1940, Texas Univ. Publ. 4032: 208-17 (fig.).
 genetics: Homozygous viable and fertile.
#
T(1;4)A11
 cytology: Chromosome 4 appended to X as second arm.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: Stone, 1934, Genetica 16: 506-20.
  Painter and Stone, 1935, Genetics 20: 327-41 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 65-72.
 genetics: Same as T(1;4)A5.
#
T(1;4)A13
 cytology: T(1;4)18C5-D1 (1940, Texas Univ. Publ. 4032: frontispiece).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: 1934, Am. Naturalist 68: 359-69.
  Stone, 1934, Genetica 16: 506-20.
  Patterson, Stone, and Bedichek, 1935, Genetics
  20: 259-79.
  1937, Genetics 22: 407-26.
  Pipkin, 1940, Texas Univ. Publ. 4032: 126-56.
 genetics: X chromosome broken between fu and car
  and in chromosome 4 to the right of ey.
  Homozygous viable and fertile. No ci position
  effect. The 4[D]X[P] element sterile in male
  and fertile in female. Complementary X[D]4[P]
  produces fertile hypotriploid females when added to
  triploid intersex phenotype; it produces a virtually
  lethal superfemale when added to normal diploid
  female genotype.
#
T(1;4)A14
 cytology: Chromosome 4 appended to X as second arm.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche, 1933.
 references: Stone, 1934, Genetica 16: 506-20.
  Painter and Stone, 1935, Genetics 20: 327-41 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 65-72.
 genetics: Translocation involves short arm of one chromosome
  and base of long arm of the other. Stone (1934),
  but not Brown (1940), reports strong reduction in
  crossing over at base of X chromosome.
#
T(1;4)A17
 cytology: T(1;4)7F5-8B1 (1940, Texas Univ. Publ. 4032: frontispiece).
 origin: X ray induced.
 discoverer: Mickey.
 references: Patterson, Stone, and Bedichek, 1937, Genetics 22: 407-26.
  Pipkin, 1940, Texas Univ. Publ. 4032: 126-56.
 genetics: X chromosome broken between t and lz,
  although the reported cytological breakpoint is to
  the left of this interval. The X[D]4[P] element
  survives when added to either a normal diploid
  female or a triploid intersex genotype; at least in the latter,
  the product is a fertile female. The
  complementary 4[D]X[P] is virtually lethal when
  added to a diploid female genotype but produces
  partially fertile females when added to a triploid
  intersex genotype.
#
T(1;4)B[S]: Translocation (1;4) Bar of Stone
 cytology: T(1;4)15F9-16A1;16A7-B1;102F (Griffen, 1941,
  Genetics 26: 154-55.
 new order:: 1 - 16A7|102F - 100;
  20 - 16A1|102F.
 origin: X ray induced in Dp(1;1)B =
  Dp(1;1)15F9-16A1;16A7-16B1.
 discoverer: Stone, 1931.
 synonym: T(1;4)1; T(1;4)4; T(1;4)A4.
 references: 1934, Genetica 16: 506-20.
 genetics: Position effect at B more extreme than in
  treated chromosome. Male and homozygous female
  viable and fertile. The 4[D]X[P] segregant
  carries no known markers from chromosome 4 and
  B[S] through bb[+] from X. Female
  hyperploid for this element viable and fertile.
  Hyperploid male poorly viable and sterile.
 genetics: Used by Stern in cytological demonstration of
  crossing over (1931, Biol. Zentr. 51: 547-87).
  4[D]X[P] from T(1;4)B[S] used by Lindsley and
  Sandler [1963, in Methodology in Basic Genetics
  (W. J. Burdette, ed.). Holden-Day, Inc., pp. 390-403]
  in construction of compound-generating
  B[S] duplications. Reciprocal products of
  meiosis in male not always recovered with equal
  frequency (Novitski and Sandler, 1957,
  Proc. Natl. Acad. Sci. U.S. 43: 318-24; Zimmering, 1960,
  Genetics 45: 1253-68; Zimmering and Barbour, 1961,
  Genetics 46: 1253-60; Zimmering and Perlman, 1962,
  Can. J. Genet. Cytol. 4: 333-36).
#
T(1;4)ct[13b1]: Translocation (1;4) cut
 cytology: T(1;4)7B2-3;20;101A-D superimposed on
  R(1)1A3-4;19F-20A1.
 new order:: |1A4 - 7B2|20.20F -
  20A1|;
  101A|7B3 - 20|101D - 102;
  Tentative.
 origin: X ray induced in R(1)2.
 discoverer: Hannah, 1947.
 genetics: Mutant for ct but not y, ac, sc, cm, sn, or
  oc. Male lethal.
#
T(1;4)l-v11: Translocation (1;4) lethal-variegated
 cytology: T(1;4)15;101.
 origin: X ray induced.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1649-70.
 genetics: Variegated for a lethal. Male fertile.
#
T(1;4)M-pro: Translocation (1;4) Minute-producer
 discoverer: Bridges, 33d26.
 synonym: M-pro: Minute-producer.
 genetics: Minutes produces are haplo-4's. The
  translocation causes nondisjunction of
  chromosome 4 centromeres (L. V. Morgan, 1940,
  DIS 13: 51).
#
T(1;4)N[264-12]: Translocation (1;4) Notch
 cytology: T(1;4)3C6-7;101F (Sutton).
 origin: X ray induced.
 discoverer: Demerec, 34a.
 synonym: T(1;4)N[a8].
 references: 1941, Proc. Intern. Congr. Genet., 7th., pp. 99-103.
  Judd, 1955, DIS 29: 126-27.
 genetics: Carries mutant allele of N. Variegates for
  w and rst but not pn, kz, or dm. The
  ci[+] allele shows weakened dominance (Stern).
#
T(1;4)N[264-20]
 cytology: T(1;4)3C4-5;3C7-8;101F; 3C5-7 missing
  (Sutton).
 new order:: 1 - 3C4|101F;
  20 - 3C8|101F - 102.
 origin: X ray induced.
 discoverer: Demerec, 34g.
 genetics: Deficient for N; variegates for w and
  rst but not pn, kz, or dm. ci[+] shows
  weakened dominance (Stern).
#
T(1;4)N[264-86]
 cytology: T(1;4)3C6-7;3C7-8;3E5-6;101F.
 new order:: 1 - 3C7|3E6 - 20;
  101A - 101F|3C7 - 3E5|101F - 102;
  band 3C7 present twice
  and considered to have been from each of two
  chromatids in the sperm (Demerec and Sutton, 1940,
  Proc. Natl. Acad. Sci. U.S. 26: 532-36).
 origin: X ray induced.
 discoverer: Demerec, 39i.
 references: 1940, Genetics 25: 618-27.
  Sutton, 1940, Genetics 25: 534-40 (fig.).
 genetics: Carries two N loci, one mutant and one
  variegated. Also carries a mutant allele of rst
  (rst[264-86]) and variegates for dm but not
  w or ec. Carries normal allele of ci[+]
  (Stern). Dp(1;4)N[264-86] =
  Dp(1;4)3C6-7;3E5-6;101F-102 viable and fertile in
  both sexes; Df(1)N[264-86] = Df(1)3C7-8;3E5-6
  viable in heterozygote.
#
T(1;4)N[264-113].
 cytology: T(1;4)3C10-D1;101; section 102 missing.
 new order:: 1 - 3C10|101;
  20 - 3D1|?.
  Proximal portion of X chromosome considered to
  be terminally deficient although it occasionally
  appears to be capped by a small nucleolus-like
  structure [Sutton, 1940, Genetics 25: 628-35
  (fig.)]. Not clear that a reciprocal translocation
  between X and short arm of 4 was adequately
  ruled out.
 origin: X ray induced.
 discoverer: Demerec, 40c.
 genetics: Variegates for w and N but not ac, sc,
  dm, or ec. Carries normal allele of ci
  (Stern).
#
T(1;4)sc[10-2]: Translocation (1;4) scute
 cytology: T(1;4)1D;101E-F [+ T(1;4)1A;102F according
  to Schultz].
 new order:: 1A|102F - 101F|1D - 20;
  101A - 101F|1D - 1A|102F;
  Tentative.
 origin: X ray induced in ac[3].
 discoverer: Sturtevant, 1930.
 references: 1934, Proc. Natl. Acad. Sci., U.S. 20: 515-18.
  1936, Genetics 21: 444-66.
 genetics: Mutant for sc. Virtually male lethal. X
  chromosome broken between M(1)Bld and br;
  chromosome 4 broken proximal to ci.
  According to Schultz, both X and 4 also have
  breaks distal to all known loci and their termini
  are interchanged. X[D]4[P] carries
  X-chromosome loci from y through M(1)Bld
  and was used extensively by Sturtevant (1934, 1936)
  in his studies on preferential segregation. The
  4[D]X[P] element survives in the heterozygous
  female but is an extreme Minute and rarely fertile.
#
T(1;4)sc[H]: Translocation (1;4) scute of Hackett
 cytology: T(1;4)1B4-C3;101-102; inferred from genetic
  results.
 origin: Gamma ray induced.
 discoverer: Hackett, 46a.
 references: Muller and Valencia, 1947, DIS 21: 70.
 genetics: Two halves of the translocation may be recovered
  separately. 4[D]X[P] is deficient for y and
  sc but not M(1)Bld and carries ey[+].
  X[D]4[P] covers Df(1)sc[19] and therefore
  carries a normal allele of l(1)sc.
  T(1;4)sc[H]/ci is ci[+].
#
T(1;4)w[258-43]
 cytology: T(1;4)3C3-5;102F4-5 (Demerec).
 origin: X ray induced.
 discoverer: Demerec, 38k.
 genetics: Mutant for w but not kz, pn, rst, or fa.
  Male lethal.
#
T(1;4)w[m5]: Translocation (1;4) white-mottled
 cytology: T(1;4)3C3-4;101F1-2 (Griffen and Stone, 1938,
  Genetics 23: 149).
 origin: X ray induced.
 discoverer: Muller, 1929.
 synonym: T(1;4)m[5]: Translocation (1;4) mottled-5; T(1;4)A5.
 references: 1930, J. Genet. 22: 299-334.
  Bolen, 1931, Am. Naturalist 65: 417-22.
 genetics: Variegates for w and ci [Dubinin, Sokolov,
  and Tiniakov, 1935, Biol. Zh. (Moscow) 4: 716-20].
  X chromosome broken between l(1)3C3 and
  rst, and chromosome 4 broken to the left of
  ey. X[D]4[P] added to a normal male genome
  produces males with 20% normal viability that are
  weakly fertile; added to a diploid female genome, it
  produces fertile hyperploid genome; and added to a
  triploid intersex genome, it is virtually lethal.
  4[D]X[P] is inviable when added to a male genome,
  is virtually lethal when added to a female genome,
  and produces rather fertile hypotriploid females when
  added to a triploid intersex genome (Pipkin, 1940,
  Texas Univ. Publ. 4032: 126-56). Griffen and Stone
  (1940, Texas Univ. Publ. 4032: 190-200) produced
  and studied a number of X-ray-induced derivatives of
  T(1;4)w[m5].
#
T(1;4)w[m11]
 cytology: T(1;4)3C3-4;101A-D.
 origin: X ray induced.
 discoverer: Panshin.
 references: Panshin and Khvostova, 1938, Biol. Zh. (Moscow) 7: 359-80.
  Panshin, 1938, Nature 142: 837.
  1941, DIS 15: 33-34.
 genetics: Variegated for w but not ci. First
  rearrangement to involve, and therefore to
  demonstrate, existence of 4L. Panshin and
  Khvostova [1938; Panshin, 1938, Biol. Zh. (Moscow)
  7: 837-65] produced and studied a number of
  X-ray-induced derivatives of T(1;4)W[m11].
#
T(1;4)w[m51c]
 cytology: T(1;4)3C1-2;3C4-7;20A;101.
 new order:: 1 - 3C1|20A - 3C7|20A - 20F;
  101|(3C2 - 3C4)|101 - 102.
 origin: X ray induced in In(1)w[m4] = In(1)3C1-2;20A.
 discoverer: Lefevre, 51c20.
 references: 1951, DIS 25: 71.
  1952, DIS 26: 66.
  Ratty, 1954, Genetics 39: 513-28.
 genetics: Variegated for w and rst. Male lethal.
  Dp(1;4)w[m51c] = Dp(1;4)3C2-3;3C4-7;101 viable
  and fertile; carries loci of w and rst but
  not spl.
#
T(1;4)w[52b13]
 cytology: T(1;4)2A2-3;3C3-4;20B;101.
 new order:: 1 - 2A2|20B - 3C4|20B - 20F;
  101|(2A3 - 3C3)|101 - 102.
 origin: X ray induced in In(1)rst[3] = In(1)3C3-4;20B.
 discoverer: Ratty, 52b13.
 references: Lefevre, 1953, DIS 27: 57.
 genetics: Variegated for w.
#
T(1;4)w[m258-18]
 cytology: T(1;4)3C4-5;101.
 origin: X ray induced.
 discoverer: Demerec, 33k.
 references: Demerec and Slizynska, 1937, Genetics 22: 641-49.
 genetics: Variegated for w and rst but not pn, fa,
  dm, or ec. Also variegated for ci
  (Stern). Male and homozygous female viable and
  fertile. X chromosome broken between rst
  and vt (Gersh, 1965, Genetics 51: 477-80).
  The X[D]4[P] element survives as a duplication.
#
T(1;4)w[m258-21]
 cytology: T(1;4)3E5-6;101F (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 1934.
 synonym: T(1;4)w[vD3]: Translocation (1;4) white-variegated of Demerec.
 genetics: Variegates for w, fa, spl, N, dm, and M(1)3E
  but not ec or bi. Also variegates for ci
  (Gersh). Males usually lethal; survivors probably
  X/Y/Y. Cell lethal in X/0 tissue in
  gynandromorphs (Judd, 1953, DIS 27: 95).
#
T(1;4)w[m258-31]
 cytology: T(1;4)3C3-5;102F4-17 (Demerec and Hoover).
 origin: X ray induced.
 discoverer: Demerec, 37l.
 genetics: Variegated for w but not rst. Male viable.
#
T(1;4)w[m258-53]
 cytology: T(1;4)3C1-2;101E-F; distal part of
  chromosome 4 lost. Sutton thought it a
  terminal deficiency of X. Evidence that
  chromosome 4 is involved seems equivocal,
  especially since, according to events postulated,
  the original mottled fly should have been
  haplo-4. Alternative interpretation is
  translocation between X and Y in X/Y
  sperm.
 new order:: 1A - 3C1|101E - 101A;
  20 - 3C2|?.
 origin: X ray induced.
 discoverer: Demerec, 39l.
 references: Sutton, 1940, Genetics 25: 628-35.
 genetics: Variegated for w but not pn, rst, or spl.
  Male viable. Translocation-bearing fly carries two
  normal fourth chromosomes.
#
T(1;4)w[mA] Translocation (1;4) white-mottled from Austin
 cytology: T(1;4)3C2-3;101A2-3.
 origin: X ray induced.
 discoverer: Stone.
 references: Griffen and Stone, 1939, Genetics 24: 73.
  1940, Texas Univ. Publ. 4032: 201-7 (fig.).
 genetics: Variegated for w. Male viable and fertile.
  Second demonstration of the existence of a left arm
  on chromosome 4.
#
T(1;4)w[mD3]: Translocation (1;4) white-mottled of Dubinin
 cytology: T(1;4)3C;101.
 discoverer: Dubinin.
 references: Sacharov, 1936, Biol. Zh. (Moscow) 5: 293-302.
 genetics: Variegated for w.
#
T(1;4)w[mDV4] Translocation (1;4) white-mottled of Dubinin and Volotov
 cytology: T(1;4)3C3-7;3D;101A-D; 3C-3D missing; inferred
  from genetic data and from figs. 5-7 of Sacharov
  (1936) which indicate that the break in
  chromosome 4 is in the left arm.
 new order:: 1 - 3C3|101D - 102F;
  20 - 3D|101A.
 discoverer: Dubinin and Volotov.
 references: Sacharov, 1936, Biol. Zh. (Moscow) 5: 293-302
  (fig.).
 genetics: Deficient for N; variegated for w. Male
  lethal. Since the X[D]4[P] element of
  T(1;4)w[mDV4] survives as a duplication and
  carries w[mDV4], the left break in X
  chromosome is between w and N.
#
T(1;4)w[mJ]: Translocation (1;4) white-mottled of Jonsson
 cytology: T(1;4)3C2-3;20;102C.
 new order:: 1 - 3C2|20 - 3C3|102C - 101A;
  20|102C - 102F.
 origin: X ray induced.
 discoverer: Jonsson, 61i28.
 references: Lefevre, 1963, DIS 37: 49.
  Lefevre and Wilkins, 1966, Genetics 53: 175-87.
 genetics: Variegated for w. The 4[D]X[P] element of
  the translocation has become separated from the
  X[D]4[P] element and lost.
  The X[D]4[P]
  element is viable as an X/Y male but lethal as
  an X/0 male, probably owing to deficiency for
  bb. Additional evidence for appreciable
  deficiency for proximal X heterochromatin is
  virtually random disjunction of X and Y
  chromosomes. X[D]4[P] carries
  ci[+] but not ey[+].
  The variegation of white is unorthodox because
  heterochromatin has been moved to the white locus
  rather than white moved into proximal heterochromatin.
#
T(1;4)w[mMed] Translocation (1;4) white-mottled of Medvedev
 discoverer: Medvedev, 1934.
 genetics: Variegated for w and probably rst. Arose in
  w[a] and therefore has light eye color.
#
T(1;4)z[20G1]: Translocation (1;4) zeste
 discoverer: T(1;4)3C1-2;102F2-4; genetic data more in
  accord with breakpoint in 3C2-3 than 3C1-2.
 origin: X ray induced in a chromosome carrying z.
 discoverer: Gans.
 references: 1953, Bull. Biol. France Belg. Suppl. 38: 1-90
  (fig.).
  Gersh, 1963, DIS 37: 80.
 genetics: Suppresses z. The X[D]4[P] element is
  poorly viable when added to male genome but viable
  and fertile in female; duplicated for w but does
  not cover lethality of Df(1)w[m4L]rst[3R] =
  Df(1)3C1-2;3C3-4 (Gersh, 1963).
#
T(1;A)pn-ec: Translocation (1;Autosome) prune-echinus
 cytology: T(1;A)2D1-2;3F7-4A1;40-41 or 80-81;
  position of autosomal breakpoint not determined.
 new order:: 1 - 2D1|4A1 - 20;
  21 - 40|(2D2 - 3F7)|41 - 60;
  (for example).
 origin: X ray induced.
 discoverer: Robins, 62g26.
 references: Lefevre, 1963, DIS 37: 50.
 genetics: w not affected. Male lethal. Female
  heterozygous for the segregant Df(1)pn-ec =
  Df(1)2D1-2;3F7-4A1 survives though poorly viable
  and fertile. Male heterozygous for complementary
  Dp(1;A)pn-ec = Dp(1;A)2D1-2;3F7-4A1;40-41 or
  80-81 viable and sterile.
  T(X.)In[x and 3]: seef3 T(1;2)w[m53e]
#
T(Y;2)21E
 cytology: T(Y;2)21D4-E1.
 discoverer: Schultz.
 references: Lewis, 1945, Genetics 30: 137-66.
 genetics: Not mutant for S or ast. Chromosome 2
  broken between ds and S. Both 2L[D]Y[P]
  and Y[D]2[P] recoverable in aneuploid progeny.
#
T(Y;2)54a
 cytology: T(Y;2)Y[L];59C4-6.
 discoverer: Mickey, 54a.
 references: 1959, Texas Univ. Publ. 5914: 99-105.
  1963, DIS 38: 30.
 genetics: Variegated for bw. Male fertile. Male
  hyperploid for Y[P]2R[D] survives, is not
  variegated, and is sterile.
#
T(Y;2)A
 cytology: T(Y;2)40F-41A1; placed in 2R by
  Whittinghill (1937, DIS 8: 82-84).
 origin: X ray induced.
 discoverer: Dobzhanksy, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbungslehre 60: 235-86.
 genetics: Break between pr and tk. rl, M(2)S2, stw, ap,
  msf, tk, and ltd not affected.
#
T(Y;2)A3: Translocation (Y;2) from Austin
 origin: X ray induced.
 discoverer: Stone.
 genetics: Variegated for bw.
#
T(Y;2)B
 cytology: T(Y;2)40F-41A1; placed in 2R by Whittinghill
  (1937, DIS 8: 82).
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbungslehre 60: 235-86.
 genetics: Lethal in combination with M(2)S2[10] and shows
  an extreme rl phenotype with rl. stw, ap,
  msf, tk, and ltd not affected.
#
T(Y;2)bw[+]Y: Translocation (Y;2) brown-wild type Y
 cytology: T(Y;2)Y[L];58F1-59A2;60E3-F1 (Gersh, 1956, DIS
  30: 115; Nicoletti).
 new order:: Y[LD]|(59A2 - 60E3)|Y[LP] - Y[S];
  21 - 58F1|60F1 - 60F5.
 origin: X ray induced.
 discoverer: Dempster.
 references: Brosseau, Nicoletti, Grell, and Lindsley, 1961,
  Genetics 46: 339-46.
 genetics: Dp(2;Y)bw[+] carries loci from bw through
  ba but not hv or M(2)c; it is used as
  a marked Y and referred to as bw[+]Y.
#
T(Y;2)bw[R27]: Translocation (Y;2) brown-Rearranged
 cytology: T(Y;2)59D11-E1.
 origin: X-ray-induced derivative of bw.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R27].
#
T(Y;2)bw[R57]
 cytology: T(Y;2)59D5-6.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R57].
#
T(Y;2)C
 cytology: T(Y;2)40F-41A1; placed in 2R by
  Whittinghill (1937, DIS 8: 82-84).
 origin: X ray induced.
 discoverer: Dobzhanksy, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbungslehre 60: 235-86.
 genetics: Does not affect rl, M(2)S2, stw, ap, msf, tk, or
  ltd.
#
T(Y;2)dp[61d]: Translocation (Y;2) dumpy
 origin: X ray induced.
 discoverer: Thompson, 61d.
 genetics: Mutant for dp.
#
T(Y;2)dp[w2]: Translocation (Y;2) dumpy-warped
 origin: X ray induced.
 discoverer: Schalet, 55k.
 references: Carlson and Schalet, 1956, DIS 30: 71.
  Carlson, 1958, DIS 32: 117-18.
 genetics: Variegated for dp.
#
T(Y;2)E
 cytology: T(Y;2)36D2-3 (Whittinghill, 1937, DIS 8: 82-84).
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbungslehre 60: 235-86.
 genetics: Male fertile; Df(1)sc[4L]sc[8R]/T(Y;2)E male is
  sterile.
#
T(Y;2)G
 cytology: T(Y;2)36B5-C1;40F; metaphase chromosomes
  appear normal (Morgan, Bridges, and Schultz, 1935,
  Carnegie Inst. Wash. Year Book 34: 287).
 new order:: Y[D]|(36C1 - 40F)|Y[P];
  21 - 36B5|40F - 60.
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  Rhoades, 1931, Genetics 16: 490-504.
 genetics: Dp(2;Y)G has normal phenotype and is fertile when
  hyperploid in either sex; duplicated for the loci of
  M(2)m, M(2)H, hk, pr, Bl, lt, and the lethal of
  bw[V32g] but not rd.
#
T(Y;2)H
 cytology: T(Y;2)37B1-2;40B2-3; also an inversion in 2R
  from near centromere to left of px (Morgan,
  Bridges, and Schultz, 1935, Carnegie Inst. Wash. Year
  Book 34: 287).
 new order:: Y[D]|(37B2 - 40B2)|Y[P];
  21 - 37B1|40B3 - | - | - 60.
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  Schultz and Bridges, 1932, Am. Naturalist 66: 323-34.
 genetics: Male fertile. Homozygote viable and male sterile.
  Df(2L)H survives and is deficient for M(2)H,
  hk, and pr but not M(2)m or lt;
  somewhat sterile. Dp(2;Y)H appears normal;
  duplicated for the loci for which Df(2L)H is
  deficient.
#
T(Y;2)J
 cytology: T(Y;2)40F-41A1;57F1-2 (Whittinghill, 1937, DIS
  8: 82-84).
 new order:: Y[D]|40F - 21;
  Y[P]|57F1 - 41A1|57F2 - 60.
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbugnslehre 60: 235-86.
 genetics: Does not affect rl, M(2)S2, stw, ap, msf, tk, or
  ltd.
#
T(Y;2)R24
 cytology: T(Y;2)45A;51E.
 new order:: Y[D]|(45A - 51E)|Y[P];
  21 - 45A|51E - 60.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 8.
 genetics: Induced simultaneously with (but independently of)
  bw[24], an isoallele of bw. Associated with
  a rough eye phenotype. Male hyperploid for
  Dp(2;Y)R24 is viable and sterile.
#
T(Y;2)w[+]Y
  Described as w[+]Y (see Y
  Derivatives in Special Special
  Chromosomes Chromosomes section).
#
T(Y;2;3)D
 cytology: T(Y;2;3)29F-30A1 + T(2;3)34C;78F + Df(2R)41A;41C +
  Df(3L)61E2-F1;62A4-6. May also carry small inverted
  segment in region 41 (Whittinghill, 1937, DIS 8: 82-84).
 new order:: Y[D]|30A1 - 34C|78F - 100;
  Y[P]|29F - 21;
  60 - 41C|41A - 34C|78F - 62A6|61E2 - 61A.
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 synonym: T(Y;2)D.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbungslehre 60: 235-86.
 genetics: Deficient for M(2)S2 and stw (but not rl,
  ap, msf, tk, or ltd) in chromosome 2 and
  for ru, aa, and ve [but not su(ve) or
  R] in chromosome 3. The 2L[D]Y[P]
  element survives in hyperploids.
#
T(Y;2;3)F
 origin: X ray induced.
 discoverer: Dobzhanksy, 1929.
 synonym: T(Y;2)F.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbungslehre 60: 235-86.
 genetics: Break in 2R to right of sp.
#
T(Y;2;3)l
 cytology: T(Y;2)47A2-3 + T(Y;3)91E2-4 + In(3LR)69C2-3;84E2-3
  + In(3LR)74A-B1;99C (Whittinghill, 1938, DIS 8: 82-84).
 new order:: Y[D]|47A2 - 21;
  Y[D]|91E4 - 99C|74B1 - 84E2|69C2 - 61;
  60 - 47A3|Y[P]|91E2 - 84E3|69C3 -
  74A|99C - 100.
 origin: X ray induced.
 discoverer: Dobzhanksy, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1932, Z. Induktive Abstammungs- Vererbungslehre
  69: 235-86.
#
T(Y;3)42i
 cytology: Break in middle of one arm of chromosome 3.
 origin: X ray induced.
 discoverer: Poulson.
 references: 1943, DIS 17: 51.
#
T(Y;3)H[58b]: Translocation (Y;3) Hairless
 origin: Gamma ray induced.
 discoverer: Ives, 58b25.
 references: 1959, DIS 33: 95.
 genetics: Mutant for H.
#
T(Y;3)l
 cytology: T(Y;3)Y[S];63C;72E.
 new order:: Y[L] - Y[SP]|63C - 72E|63C - 61;
  Y[SD]|72E - 100.
 origin: X ray induced.
 discoverer: Muller.
 references: Painter and Muller, 1929, J. Heredity 20: 287-98.
  Muller, 1930, J. Genet. 22: 299-334.
  Mohr and Mossige, 1940, Hereditas 26: 202-8 (fig.).
 genetics: Right break in 3L between th and st. The
  3L[D]Y[P] element recoverable in hyperploid and
  duplicated for loci from ru through th.
#
T(Y;3)K4: Translocation (Y;3) of Krivshenko
 cytology: T(Y;3)Y[S];81; inferred from metaphase
  cytology. Ganglion metaphases show break in
  Y[S] distal to bb and break in 3R near
  centromere.
 origin: X ray induced.
 discoverer: Krivshenko, 59b7.
 references: 1959, DIS 33: 96.
 genetics: Homozygous viable and apparently sterile.
#
T(Y;3)P80: Translocation (Y;3) from Pasadena
 cytology: T(Y;3)88C-F.
 discoverer: E. B. Lewis.
#
T(Y;3)P102
 cytology: T(Y;3)87B2-3.
 discoverer: E. B. Lewis.
#
T(Y;3)sr[100.23]: Translocation (Y;3) stripe
 cytology: T(Y;3)90E2-3.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for sr.
#
T(Y;3)st[100.126]: Translocation (Y;3) scarlet
 cytology: T(Y;3)73A2-3.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for st.
#
T(Y;4)
  Described as 4Y (see Y
  Derivatives in Special Special
  Chromosomes Chromosomes section).
#
T(2;3)63-1
 cytology: T(2;3)49D-E;79B-C.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous viable and fertile. Eyes slightly rough.
#
T(2;3)63-2
 cytology: T(2;3)27B-C;75C.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-3
 cytology: T(2;3)40-41;80-81; inferred from genetic
  results because salivary chromosomes appear normal.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-5
 cytology: T(2;3)40C;89E-F + In(3L)69-70;79-80.
 new order:: 21 - 40C|89E - 80|70 - 79|69 - 61;
  60 - 40C|89F - 100.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)63-6
 cytology: T(2;3)59E-F;89E-F.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous viable and fertile. Short bristles; wings
  obliquely creased, ovate, and often asymmetrical.
#
T(2;3)63-7
 cytology: T(2;3)41C;92D-E.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-8
 cytology: T(2;3)36E;86B.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-9
 cytology: T(2;3)34A-B;75C.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-10
 cytology: T(2;3)33-34;76D-E.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous viable and sterile. Abdominal tergite
  pigmentation more intensive and extensive than wild
  type.
#
T(2;3)63-13
 cytology: T(2;3)24-25;94D-E.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous viable and fertile. Eye color
  variegated.
#
T(2;3)63-14
 cytology: T(2;3)38A-B;69A-B.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-15
 cytology: T(2;3)41D;64A.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal. Eye color variegated in
  heterozygote.
#
T(2;3)63-16
 cytology: T(2;3)41C-D;93A-B.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous viable and fertile. Eyes slightly
  rough.
#
T(2;3)63-17
 cytology: T(2;3)40C;96A-B.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal. Eye color in heterozygote
  variegated over SM5 but normal over bw and
  +. Possibly contains light-mottled.
#
T(2;3)63-18
 cytology: T(2;3)39B-C;80C.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous viable and fertile. Ninety percent have
  trough-like wing posture.
#
T(2;3)63-19
 cytology: T(2;3)24D-E;80C.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-21
 cytology: T(2;3)32E;89C-E + In(3LR)65B;84B.
 new order:: 21 - 32E|89C - 84B|65B - 84B|65B - 61;
  60 - 32E|89E - 100.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)63-22
 cytology: T(2;3)40B;84D.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)63-23
 cytology: T(2;3)40-41;80-81; inferred from genetic data
  because salivary chromosomes appear normal.
 origin: Gamma ray induced.
 discoverer: C. Hinton, 63b.
 references: 1964, DIS 39: 61.
  1965, Genetics 51: 971-82.
 genetics: Homozygous lethal.
#
T(2;3)64-31
 cytology: T(2;3)36D-E;96B-C + In(2R)41E-F;55F.
 new order:: 21 - 36D|96B - 61;
  60 - 55F|41F - 55F|41E - 36E|96C - 100.
 origin: X ray induced.
 discoverer: C. Hinton, 1964.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)64-32
 cytology: T(2;3)35D-E;70C-D.
 origin: X ray induced.
 discoverer: C. Hinton, 1964.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)64-33
 cytology: T(2;3)40-41;80-81; inferred from genetic data
  because salivary chromosomes appear normal.
 origin: X ray induced.
 discoverer: C. Hinton, 1964.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)64-34
 cytology: T(2;3)25D;86C.
 origin: X ray induced.
 discoverer: C. Hinton, 1964.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)64-35
 cytology: T(2;3)40B;92C.
 origin: X ray induced.
 discoverer: C. Hinton, 1964.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)64-36
 cytology: T(2;3)40D;85E.
 origin: X ray induced.
 discoverer: C. Hinton, 1964.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)64-37
 cytology: T(2;3)60E;82F.
 origin: X ray induced.
 discoverer: C. Hinton, 1964.
 references: 1965, Genetics 51: 971-82.
#
T(2;3)100r20
 cytology: T(2;3)35B2;3;40;80 superimposed on
  Dp(1;3)3B4-C1;4B4-5;80.
 new order:: 21 - 35B2|4B4 - 3C1|80 - 100;
  60 - 40|35B3 - 40|80 - 61.
 origin: X ray induced in Dp(1;3)N[264-100].
 discoverer: Gersh, 1959.
 references: 1959, Genetics 44: 163-72.
 genetics: Selected as a partial reversion from white-mottled.
#
T(2;3)101
 cytology: T(2;3)44B;83E-F (Lewis, 1956, DIS 30: 130).
 discoverer: Sturtevant.
 genetics: Homozygous viable; male fertile and female sterile.
  Crossing over about normal in chromosome 2 of
  heterozygous female.
#
T(2;3)103
 discoverer: Sturtevant.
 genetics: Homozygous lethal. Reciprocal translocation with
  breaks in 2L and 3L. Crossing over in
  heterozygous female low in 2L, normal in 2R.
#
T(2;3)108
 cytology: T(2;3)37-40;42A2-3;52D-F;58A4-B1;80;81;
  inferred from a combination of cytological [52D-F
  (Lewis, 1951, DIS 25: 108-9)] and genetic
  observations.
 new order:: 21 - 37|(80 - 81)|52D - 42A3|58B1
  - 60;
  61 - 80|(40 - 42A2|58A4 - 52F)|81 - 100.
 origin: Arose in In(2R)Cy = In(2R)42A2-3;58A4-B1.
 discoverer: Sturtevant.
 genetics: Mutant for Rev. Homozygous semilethal. The
  segregant that receives a normal chromosome 2
  and the translocated element that might be
  designated 3L[D]2[P]3R[D] survives and is
  fertile. It is duplicated for the loci of pr, lt,
  rl, tk, and according to E. B. Lewis, for
  M(2)S7, sm, and hy; not deficient for
  chromosome 3 genes.
#
T(2;3)109
 cytology: T(2;3)22F-23B;55F-56A;80 (Lewis, 1951, DIS
  25: 108-9).
 new order:: 21 - 22F|55F - 23B|80 - 61;
  60 - 56A|80 - 100.
 discoverer: Sturtevant.
 genetics: Homozygous viable and wild type. Originated in
  In(3R)P but is separable from it.
#
T(2;3)110
 origin: X ray induced.
 discoverer: Sturtevant.
 genetics: Homozygous lethal. Wings short, extended, and coiled
  downward in spiral. L4 and marginal veins
  thickened, L4 sometimes not reaching margin;
  posterior wing cell reduced. Posterior crossvein
  absent; L5 reduced and irregularly plexate. Break in
  2R near vg and one in 3R, which carries
  In(3R)P. New order is 2L + 3L and 2R + 3R.
#
T(2;3)135
 cytology: T(2;3)37;85A.
 origin: X ray induced simultaneously with T(1;2)l-v135.
 discoverer: Lindsley, Edington, and Von Halle.
 references: 1960, Genetics 45: 1663.
#
T(2;3)A
 cytology: T(2;3)39B-C;83B (Lewis, 1951, DIS 25: 108-9).
 origin: X ray induced in Bl.
 discoverer: Dobzhansky, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  1933, Z. Induktive Abstammungs- Vererbungslehre
  64: 269-309.
  Dobzhansky and Sturtevant, 1931, Carnegie
  Inst. Wash. Publ. No. 421: 29-59.
 genetics: Homozygous lethal.
#
T(2;3)A1: Translocation (2;3) from Austin
 origin: X ray induced.
 references: Patterson, Stone, Bedichek, and Suche, 1934,
  Am. Naturalist 68: 359-69.
  Pipkin, 1940, Texas Univ. Publ. 4032: 73-125.
 genetics: Homozygous viable and fertile. Chromsomes 2
  and 3 broken at chromocenter. 2L attached
  to 3R and 3L to 2R.
#
T(2;3)A26
 origin: X ray induced.
 discoverer: Muller.
 references: Painter and Muller, 1929, J. Heredity 20: 287-98.
  Muller, 1930, J. Genet. 22: 299-334.
 genetics: Break in 3R between sr and e.
#
T(2;3)Antp[Yu] Translocation (2;3) Antennapedia of Yu
 cytology: T(2;3)22B;83E-F + T(2;3)38E;98A.
 new order:: 21 - 22B|83F - 98A|38E - 22B|83E - 61;
  60 - 38E|98A - 100.
 origin: X ray induced.
 discoverer: Yu, 1948.
 references: 1949, Ph.D. Thesis, Calif. Inst. Technol.
  Lewis, 1956, DIS 30: 76.
 genetics: Mutant for Antp; associated with 83E-F
  breakpoint. Homozygous lethal.
#
T(2;3)ap[Xa]: Translocation (2;3) apterous-Xasta
 cytology: T(2;3)41F;89E8-F1 superimposed on
  In(2R)42A2-3;58A4-B1 + In(3R)89C2-3;98A18-19
  |idges in Morgan, Bridges, and Schultz, 1936,
  Carnegie Inst. Wash. Year Book 35: 294;
  correction by Lewis, 1951, DIS 25: 108-9).
 new order:: 21 - 41F|89E8 - 89C3|96A19 - 100;
  60 - 58B1|42A3 - 58A4|42A2 - 41F|89F1
  - 96A18|89C2 - 61.
 origin: X ray induced in In(2R)Cy; In(3R)P.
 discoverer: Serebrovsky, 28a.
 synonym: T(2;3)Xa: Translocation (2;3) Xasta.
 references: Serebrovsky and Dubinin, 1930, J. Heredity 21: 259-65.
  Sturtevant, 1934, DIS 2: 19.
 genetics: Dominant mutant for ap. Homozygote virtually
  lethal.
 genetics: The first X-ray-induced mutation recovered in the
  USSR. Useful as a balancer of 2R and 3R.
#
 T(2;3)ast[rv1]: Translocation (2;3) asteroid-reverted
 cytology: T(2;3)21E2-3;68C2-3;88D8-9.
 new order:: 21A - 21E2|88D8 - 68C3|88D9 - 100;
  61 - 68C2|21E3 - 60.
 origin: X ray induced in al ast ho.
 discoverer: E. B. Lewis, 1942.
 references: 1945, Genetics 30: 158.
 genetics: Associated with a reversion of ast. Homozygous
  lethal.
#
T(2;3)ast[rv3]
 cytology: T(2;3)21E2-3;61C2-3.
 origin: X ray induced in net ast dp cl.
 discoverer: E. B. Lewis, 1942.
 references: 1945, Genetics 30: 158.
 genetics: Associated with reversion of ast. Lethal
  homozygous and heterozygous with Df(2L)S4 =
  Df(2L)21C3-4;22B2-3.
#
T(2;3)Ata: Translocation (2;3) Arista
 cytology: T(2;3)40;66F-67A + T(2;3)47;81.
 new order:: 21 - 40|67A - 81|47 - 60;
  61 - 66F|40 - 47|81 - 100.
 origin: X ray induced.
 discoverer: Krivshenko, 1949.
 synonym: T(2;3)At (symbol preoccupied).
 references: 1954, DIS 28: 74-75.
  1955, DIS 29: 73.
 genetics: Associated with Ata. Homozygous lethal.
#
T(2;3)B
 cytology: T(2;3)33;81F (Lewis, 1951, DIS 25: 108-9; 1954,
  Am. Naturalist 88: 225-38).
 origin: X ray induced.
 discoverer: Dobzhansky, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  Dobzhansky and Sturtevant, 1931, Carnegie
  Inst. Wash. Publ. No. 421: 29-59.
 genetics: Homozygous lethal. Crossing over reduced in 2L.
#
T(2;3)bw[R4]: Translocation (2;3) brown-Rearranged
 cytology: T(2;3)59E2-3;80-81.
 origin: X-ray-induced derivative of bw.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R4].
#
T(2;3)bw[R12]
 cytology: T(2;3)59D;80C.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R12].
#
T(2;3)bw[R14]
 cytology: T(2;3)59E2-3;80.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R14].
#
T(2;3)bw[R15]
 cytology: T(2;3)59D;80C.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R15].
#
T(2;3)bw[V3]: Translocation (2;3) brown-Variegated
 origin: X ray induced.
 discoverer: Muller.
 references: Glass, 1933, J. Genet. 28: 69-112.
  1934, Am. Naturalist 68: 107-14.
 genetics: Variegated for bw. Break near bw in 2R
  and in 3L just left of centromere.
 genetics: Similar to T(2;3)bw[V4] and T(2;3)bw[V5];
  translocation parts interchangeable among these
  rearrangements without altering phenotype.
#
T(2;3)bw[V4]
 origin: X ray induced.
 discoverer: Patterson.
 references: Glass, 1933, J. Genet. 28: 69-112.
  1934, Am. Naturalist 68: 107-14.
 genetics: Variegated for bw. Break in 2R near bw
  and in 3L near centromere.
#
T(2;3)bw[V5]
 origin: X ray induced.
 discoverer: Patterson.
 references: Glass, 1933, J. Genet. 28: 69-112.
  1934, Am. Naturalist 68: 107-14.
 genetics: Variegated for bw. Break in 2R near bw
  and in 3L near centromere.
#
T(2;3)bw[V6]
 origin: X ray induced in bw.
 discoverer: Moore, 1929.
 references: Glass, 1933, J. Genet. 28: 69-112.
  1934, Am. Naturalist 68: 107-14.
 genetics: Crossing over reduced in 2L, 2R, and base of
  3R. Probably breaks in all three arms.
 genetics: Eye color reverted to wild type and translocation
  remained.
#
T(2;3)bw[V8]
 origin: X ray induced.
 discoverer: Levy, 1932.
 genetics: Variegated for bw. Break in 2R at bw
  and 3R near p.
#
T(2;3)bw[V30k12]
 origin: X ray induced.
 discoverer: Van Atta, 30k12.
 references: 1932, Genetics 17: 637-59.
 genetics: Variegated for bw. Complex rearrangement with
  break in 2R near bw, near centromere of
  2, in 2L and 3L near centromere; also
  appears to carry an inversion in 3R.
#
T(2;3)bw[V30k13]
 origin: X ray induced.
 discoverer: Van Atta, 30k13.
 references: 1932, Genetics 17: 637-59.
 genetics: Variegated for bw. Breaks in 2R near c
  and bw and in 3R near cu.
#
T(2;3)bw[VD] Translocation (2;3) brown-Variegated Dichaete linked
 origin: X ray induced.
 discoverer: Oliver, 29k24.
 references: 1932, Z. Induktive Abstammungs- Vererbungslehre
  61: 447-88.
 genetics: Variegated for bw. Homozygous lethal.
#
T(2;3)bw[VDe3] Translocation (2;3) brown- Variegated of Demerec
 cytology: T(2;3)59D;81F. Also an inversion in 2R.
 origin: X ray induced.
 discoverer: Demerec, 33j14.
 genetics: Variegates for bw and mi but not abb.
  Mutant for Dfd. Homozygous lethal. Gives
  transvection effects with certain pairs of bithorax
  pseudoalleles (Lewis, 1955, Am. Naturalist 89: 73-89).
#
T(2;3)bw[VDe4]
 cytology: T(2;3)59D2-4;80 (Schultz).
 origin: X ray induced.
 discoverer: Demerec, 33k22.
 genetics: Variegates for bw and mi. Homozygous
  lethal.
#
T(2;3)C
 origin: X ray induced.
 discoverer: Dobzhansky, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  Dobzhansky and Sturtevant, 1931, Carnegie
  Inst. Wash. Publ. No. 421: 29-59.
 genetics: Break near centromere in chromosomes 2 and
  3. New order is 2L + 3L; 2R + 3R.
  Homozygous lethal.
#
T(2;3)C4 Translocation (2;3) Crossover suppressor
 cytology: T(2;3)40-41;94A; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination reduced in 3R.
#
T(2;3)C11
 cytology: T(2;3)40-41;64D;77A; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 new order:: 21 - 40|77A - 64D|77A - 100;
  60 - 40|64D - 61.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous viable. Recombination reduced in 3L.
#
T(2;3)C16
 cytology: T(2;3)50E;66C;70C.
 new order:: 21 - 50E|70C - 66C|50E - 60;
  61 - 66C|70C - 100.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination reduced in 3L
  and 2R.
#
T(2;3)C17
 cytology: T(2;3)56F;67E.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination reduced in 3L
  and 2R.
#
T(2;3)C18
 cytology: T(2;3)25B;40;84B.
 new order:: 21 - 25B|40 - 60;
  61 - 84B|25B - 40|84B - 100.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination reduced in 2L.
#
T(2;3)C24
 cytology: T(2;3)53B;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous viable. Recombination reduced in 2R.
#
T(2;3)C29
 cytology: T(2;3)43F;92D.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous viable. Recombination reduced in 3R.
#
T(2;3)C49
 cytology: T(2;3)22C-D;86E.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous viable. Recombination reduced in 2L.
#
T(2;3)C58
 cytology: T(2;3)40-41;96F; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1964.
 genetics: Homozygous lethal. Recombination reduced in 3R.
#
T(2;3)C65
 cytology: T(2;3)40-41;75A;80-81 + In(3L)64C;77A;
  involvement of chromosome 2 inferred from
  genetic data; positions of heterochromatic
  breakpoints with respect to centromeres not
  determined.
 new order:: 21 - 40|80 - 100;
  60 - 40|75A - 64C|77A - 80|75A -
  77A|64C - 61.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts and D. Stewart, 1964.
 genetics: Homozygous lethal. Recombination reduced in 3L.
#
T(2;3)C101
 cytology: T(2;3)29B;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygote survives infrequently. Recombination
  reduced in 2L.
#
T(2;3)C111
 cytology: T(2;3)40-41;70F + In(3L)62B;79D-E; position of
  breakpoint in chromosome 2 with respect to
  centromere not determined; new order therefore
  ambiguous.
 new order:: 21 - 40|70F - 62B|79E - 100;
  60 - 40|70F - 79D|62B - 61.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 3L.
#
T(2;3)C122
 cytology: T(2;3)60B;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination reduced in 2R.
#
T(2;3)C124
 cytology: T(2;3)34D;75F.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2L.
#
T(2;3)C132
 cytology: T(2;3)55E;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2R.
#
T(2;3)C149
 cytology: T(2;3)52A;93B.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2R and 3R.
#
T(2;3)C157
 cytology: T(2;3)41;96D-E + In(2LR)24F;54F.
 new order:: 21 - 24F|54F - 41|96D - 61;
  60 - 54F|24F - 41|96E - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination reduced in 2L
  and 3R.
#
T(2;3)C164
 cytology: T(2;3)32F;64B.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2L and 3L.
#
T(2;3)C177
 cytology: T(2;3)40-41;62F + T(2;3)56F;79B; position of
  left breakpoint in chromosome 2 with respect to
  centromere not determined.
 new order:: 21 - 40|62F - 79B|56F - 41|62F - 61;
  60 - 56F|79B - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  3L and 2R.
#
T(2;3)C199
 cytology: T(2;3)41;93E.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  3R.
#
T(2;3)C202
 cytology: T(2;3)56D;89D.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination reduced in 2R.
#
T(2;3)C211
 cytology: T(2;3)40-41;70C; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  3L.
#
T(2;3)C218
 cytology: T(2;3)40-41;70F; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  3L.
#
T(2;3)C230
 cytology: T(2;3)35D;61A.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  3L.
#
T(2;3)C231
 cytology: T(2;3)50D;62B + In(2LR)35C-D;52A-B.
 new order:: 21 - 35C|52B - 50D|62B - 100;
  60 - 52A|35D - 50D|62B - 61.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2R and 3L.
#
T(2;3)C248
 cytology: T(2;3)52C;94D;96B.
 new order:: 60 - 52C|94D - 61;
  21 - 52C|96B - 94D|96B - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 2R and 3R.
#
T(2;3)C257
 cytology: T(2;3)50F;80; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 2R.
#
T(2;3)C259
 cytology: T(2;3)40-41;61E;73A; position of breakpoint in
  chromosome 2 with respect to centromere not
  determined.
 new order:: 21 - 40|61E - 73A|41 - 60;
  61A - 61E|73A - 100.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 3L.
#
T(2;3)C267
 cytology: T(2;3)21D;63F;64E + In(3LR)74F;88D.
 new order:: 21A - 21D|64E - 74F|88D - 74F|88D
  - 100;
  60 - 21D|63F - 64E|63F - 61.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 3L.
#
T(2;3)C287
 cytology: T(2;3)54F;89F.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 2R.
#
T(2;3)C293
 cytology: T(2;3)43A;67A;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 new order:: 21 - 43A|67A - 61;
  60 - 43A|80 - 67A|81 - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 3L.
#
T(2;3)C304
 cytology: T(2;3)48A;83C;100B.
 new order:: 21 - 48A|100B - 100F;
  60 - 48A|83C - 100B|83C - 61.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 3R.
#
T(2;3)C308
 cytology: T(2;3)40-41;84B;94D;99B.
 new order:: 21 - 40|94D - 84B|94D - 99B|84B - 61;
  60 - 40|99B - 100.
  Tentative.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in 3R.
#
T(2;3)C309
 cytology: T(2;3)58D;68F.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2R and 3L.
#
T(2;3)C311
 cytology: T(2;3)54C;64C.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2R and 3L.
#
T(2;3)C313
 cytology: T(2;3)27B;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2L.
#
T(2;3)C316
 cytology: T(2;3)25F;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2L.
#
T(2;3)C317
 cytology: T(2;3)24D;97D.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2L and 3R.
#
T(2;3)C328
 cytology: T(2;3)55C;58B;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 new order:: 21 - 55C|58B - 60;
  61 - 80|(55C - 58B)|81 - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination reduced in
  2R. The segregant Dp(2;3)C328 =
  Dp(2;3)55C;58B;80-81 survives but not the
  complementary deficiency.
#
T(2;3)C356
 cytology: T(2;3);29F;80-81; position of breakpoint in
  chromosome 3 with respect to centromere not
  determined.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination reduced in
  2L.
#
T(2;3)C591
 cytology: T(2;3)28D;69D.
 origin: X ray induced in oocyte.
 discoverer: Roberts and Thomas, 1965.
 references: Thomas and Roberts, 1966, Genetics 53: 855-62.
 genetics: Homozygous lethal. Recombination reduced in 2L.
#
T(2;3)C-K Translocation (2;3) Curved of Krivshenko
 cytology: T(2;3)52;76;81;86.
 new order:: 21 - 52|86 - 100;
  60 - 52|81 - 76|81 - 86|76 - 61.
 origin: X ray induced.
 discoverer: Krivshenko, 55l3.
 references: 1956, DIS 30: 74.
 genetics: Associated with C-K. Homozygous lethal.
#
T(2;3)D
 origin: X ray induced.
 discoverer: Dobzhansky, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  Dobzhansky and Sturtevant, 1931, Carnegie
  Inst. Wash. Publ. No. 421: 29-59.
 genetics: Heterozygote short lived and frequently sterile,
  especially in female. Wings misshapen and legs
  short.
#
T(2;3)dp: Translocation (2;3) dumpy
 cytology: T(2;3)34D;41A;47E;48A;80;81 +
  In(2)27D1-2;32D;44C5-6;44F3-12 |idges);
  existence of break or breaks in chromosome 3
  inferred from genetic data x ller, 1942; Cooper,
  Zimmering, and Krivshenko, 1955,
  Proc. Natl. Acad. Sci. U.S. 41: 911-14).
 new order:: 21 - 27D1|32D - 34D|41A -
  44C5|44F3 - 44C6|27D2 - 32D|44F12
  - 47E|(80 - 81)|48A - 60;
  61 - 80|(34D - 41A)|81 - 100.
  Extremely tentative; 47E - 48A unaccounted for.
 origin: Reportedly spontaneous.
 discoverer: Nichols-Skoog, 36e16.
 synonym: In(2LR)dp.
 references: Morgan, Bridges, and Schultz, 1937, Carnegie
  Inst. Wash. Year Book 36: 301.
  Curry, 1939, DIS 12: 46.
  Muller, 1942, DIS 16: 64.
 genetics: Mutant for dp (dp[36e]), b
  (b[36f]), rl
  [T(2;3)dp/Df(2R)M-S2[vg11] is rl], tuf
  [T(2;3)dp/tuf is extreme tuf], and a
  lethal that is uncovered by Df(2R)Np.
  Associated with a dominant rough eye mutant.
  Homozygous lethal. The chromosome 3 segregant
  Dp(2;3)dp = Dp(2;3)34D;41A;80;81 (tentative)
  survives in poorly fertile male and sterile female,
  both of which have arched wings and low viability;
  duplicated for pr. The complementary Df(2LR)dp
  = Df(2LR)34D;41A is lethal.
#
T(2;3)dp[D]: Translocation (2;3) dumpy-Dominant
 cytology: T(2;3)25A;95B-D (E. B. Lewis).
 origin: X ray induced.
 discoverer: E. B. Lewis, 1962.
 references: Del Campo, 1963, DIS 38: 32.
 genetics: Mutant for dp. Homozygous lethal.
#
T(2;3)dp[w1]: Translocation (2;3) dumpy-warped
 origin: X ray induced.
 discoverer: Schalet, 1955.
 references: Carlson and Schalet, 1955, DIS 29: 71-72.
  Carlson, 1958, DIS 32: 117-18.
 genetics: Apparently variegated for dp. Homozygous
  lethal.
#
T(2;3)Dp-S: Translocation (2;3) with Duplication Star
 cytology: T(2;3)21D4-E1;81F superimposed on
  Dp(2;2)21D2-3;21E2-3.
 new order:: 21A - 21E2|21D3 - 21D4|81F - 61;
  60 - 21E1|81F - 100.
 origin: X ray induced in Dp(2;2)S, ast ast.
 discoverer: E. B. Lewis.
 references: 1945, Genetics 30: 137-66.
 genetics: Y-suppressible expression of ast.
#
T(2;3)Dr[L]: Translocation (2;3) Drop of Lewis
 cytology: T(2;3)44;89F-90A + In(3R)89C;95D-96B1.
 new order:: 21 - 44|89F - 89C|96B1 - 100;
  60 - 44|90A - 95D|89C - 61.
 origin: X ray induced.
 discoverer: E. B. Lewis.
 genetics: Mutant for Dr, which is probably independent of
  rearrangement.
#
T(2;3)E
 cytology: T(2;3)30B;67E (Schultz).
 origin: Spontaneous.
 discoverer: Sturtevant, 1929.
 references: Dobzhansky and Sturtevant, 1931, Carnegie
  Inst. Wash. Publ. No. 421: 29-59.
 genetics: Homozygous lethal.
#
T(2;3)gl[63d]: Translocation (2;3) glass
 origin: Gamma ray induced.
 discoverer: Ives, 63d29.
 references: 1965, DIS 40: 35.
 genetics: Mutant for gl.
#
T(2;3)h[100.271]: Translocation (2;3) hairy
 cytology: T(2;3)41;66D14-E1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for h.
#
T(2;3)HK: Translocation (2;3) Half of Krivshenko
 cytology: T(2;3)22A;61A.
 origin: X ray induced in female.
 discoverer: Krivshenko, 56l14.
 references: 1959, DIS 33: 95.
 genetics: Only the 2L[D]3[P] element recovered from the
  treated oocyte.
#
T(2;3)Hm: Translocation (2;3) Haltere mimic
 cytology: Breakpoints unknown.
 origin: X ray induced.
 discoverer: Slatis, 49b5.
 genetics: Associated with Hm.
#
T(2;3)Hn: Translocation (2;3) Henna
 cytology: T(2;3)53E-54A;77A;94F;96A (E. B. Lewis).
 new order:: 21 - 53E|77A - 61;
  60 - 54A|94F - 96A|77A - 94F|96A - 100.
  Tentative.
 origin: X ray induced.
 discoverer: Van Atta, 30k.
 references: 1932, Am. Naturalist 66: 93-95.
  1932, Genetics 17: 637-59.
 genetics: Separable from Hn, which is associated with
  Df(3L)Hn = Df(3L)66A;66B.
#
T(2;3)lt[m1]: Translocation (2;3) light-mottled
 cytology: T(2;3)40B-F;63E-F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m4]
 cytology: T(2;3)40B-F;67E.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m5]
 cytology: T(2;3)40B-F;98C.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m6]
 cytology: T(2;3)26E-F;40B-F;96E.
 new order:: 21 - 26E|40B - 26F|96E - 61;
  60 - 40F|96E - 100.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m7]
 cytology: T(2;3)40B-F;100F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m8]
 cytology: T(2;3)40B-F;92B.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m10]
 cytology: T(2;3)40B-F;64E.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m11]
 cytology: T(2;3)40B-F;96F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m13]
 cytology: T(2;3)40B-F;64F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m14]
 cytology: T(2;3)40B-F;95F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m15]
 cytology: T(2;3)40B-F;92E.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m17]
 cytology: T(2;3)40B-F;95C-D.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m18]
 cytology: T(2;3)40B-F;98A.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m19]
 cytology: T(2;3)40B-F;94B.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m21]
 cytology: T(2;3)40B-F;93D.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m23]
 cytology: T(2;3)40B-F;62F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m24]
 cytology: T(2;3)40B-F;59F;75C.
 new order:: 21 - 40B|75C - 100;
  60 - 59F|40F - 59F|75C - 61.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m27]
 cytology: T(2;3)40B-F;88E-F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m28]
 cytology: T(2;3)40B-F;97E.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m29]
 cytology: T(2;3)40B-F;99F.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m30]
 cytology: T(2;3)40B-F;99C.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m32]
 cytology: T(2;3)40B-F;97A.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m34]
 cytology: T(2;3)40B-F;61B.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m35]
 cytology: T(2;3)40B-F;64C.
 origin: X ray induced.
 discoverer: Hessler, 1957.
 references: 1958, Genetics 43: 395-403.
 genetics: Variegated for lt.
#
T(2;3)lt[m100]
 cytology: T(2;3)40;97F.
 origin: X ray induced.
 references: Baker and Rein, 1962, Genetics 47: 1399-1407.
 genetics: Variegated for lt. Homozygous lethal.
  T(2;3)Me: Translocation (2;3) Moiro'e(aa' T(2;3)Me: Translocation (2;3) Moiro'e(aa'
 cytology: T(2;3)48C1-2;59D2-3;60F;80-81 (tentative) +
  In(3LR)69E;91C + In(3R)89B;97D superimposed on
  In(3L)63C;72E1-2 (Whittinghill, 1937, DIS 8: 83);
  breakpoint in chromosome 3 with respect to
  centromere not determined; new order therefore
  ambiguous.
 new order:: 21 - 48C1|59D2 - 48C2|60F;
  61 - 63C|72E1 - 69E|91C - 97D|89B -
  81|59D3 - 60F|80 - 72E2|63C -
  69E|91C - 89B|97D - 100.
  Tentative.
 origin: X ray induced in In(3L)P, Me.
 discoverer: Muller, 1930.
 references: Glass, 1933, J. Genet. 28: 104.
 genetics: Mutant for sbd (sbd[1]). Dp(2;3)Me =
  Dp(2;3)59D2-3;60F;80-81 survives.
#
T(2;3)Me[2]
 origin: X ray induced.
 discoverer: Moore, 1929.
 references: Glass, 1933, J. Genet. 28: 69-112.
 genetics: Break in 2L near centromere. Mutant for Me.
  T(2;3)Me[So]: Translocation (2;3) Moiro'e(aa' of Sytko T(2;3)Me[So]: Translocation (2;3) Moiro'e(aa' of Sytko
 discoverer: Sytko.
 references: Agol, 1936, DIS 5: 7.
 genetics: Breaks reportedly in 2R and 3R, yet mutant
  for Me in 3L.
#
T(2;3)Met: Translocation (2;3) Metatarsi irregular
 origin: X ray induced.
 discoverer: Jonsson, 56a10.
 references: 1956, DIS 30: 73.
 genetics: Associated with Met.
#
T(2;3)MO
 origin: Spontaneous.
 discoverer: Imaizumi, 59a.
 references: 1962, Cytologia 27: 212-28.
 genetics: Breaks between cn and vg in 2R and
  between st and ss in 3R.
#
T(2;3)Mot-K: Translocation (2;3) Mottled of Krivshenko
 cytology: T(2;3)41;60D;80-81; breakpoint in
  chromosome 3 with respect to centromere not determined;
  association of arms therefore ambiguous.
 new order:: 21 - 41|80 - 61;
  60F - 60D|41 - 60D|80 - 100.
  Tentative.
 origin: X ray induced.
 discoverer: Krivshenko, 54c25.
 references: 1954, DIS 28: 75.
  1955, DIS 29: 76.
 genetics: Associated with Mot-K. Homozygous lethal.
#
T(2;3)MV: Translocation (2;3) Variegated of Mickey
 cytology: T(2;3)43E;75C.
 origin: Gamma ray induced.
 discoverer: Mickey, 54d.
 synonym: T(2;3)M[V54d].
 references: 1963, DIS 38: 30.
 genetics: Eye color variegated, more prominent in male.
#
T(2;3)Nu: Translocation (2;3) Nude
 cytology: T(2;3)24;36-37;39-40;73-74;75-76;77-78;81-82;85-86;89-90.
 origin: X ray induced.
 discoverer: Sutton, 41a27.
 genetics: Associated with Nu. Homozygous lethal.
#
T(2;3)P: Translocation (2;3) Pale
 cytology: T(2;3)58E3-F2;60D14-E2;96B5-C1 (Morgan,
  Bridges, and Schultz, 1935, Carnegie Inst. Wash. Year
  Book 34: 286).
 new order:: 21 - 58E3|60E2 - 60F;
  61 - 96B5|60D14 - 58F2|96C1 - 100.
 origin: Spontaneous.
 discoverer: Bridges, 17j16.
 references: 1919, Anat. Record 15: 357-58.
  1923, Anat. Record 24: 426-27.
  Bridges and Morgan, 1923, Carnegie
  Inst. Wash. Publ. No. 327: 184-87.
  Li, 1927, Genetics 12: 1-58.
  Kossikov and Muller, 1935, J. Heredity 26: 305-17.
  Bridges, 1937, Cytologia (Tokyo), Fujii Jub., Vol. 2: 745-55.
 genetics: Associated with P. Homozygote ordinarily lethal
  but survives in presence of bw[+]Y =
  Dp(2;Y)Y[L];58F1-59A2;60E3-F1; lethality
  therefore associated with 60D14-E2 breakpoint
   x ller, 1942, DIS 16: 64). Dp(2;3)P =
  Dp(2;3)58E3-F2;60D14-E2;96B5-C1 is viable and
  fertile; duplicated for loci of px, M(2)1, crs, bw,
  mi, abb, pd, ll, l(2)NS, sp, bs, and ba but not
  a or M(2)c. Homozygous Dp(2;3)P is
  lethal unless one chromosome 2 is Df(2R)P =
  Df(2R)58E3-4;60D14-E2. Df(2R)P with two normal
  third chromosomes is lethal.
 genetics: First translocation recorded in D. melanogaster.
#
T(2;3)P23: Translocation (2;3) from Pasadena
 cytology: T(2;3)81F;56F.
 origin: X ray induced in Ubx e[4].
 discoverer: E. B. Lewis, 49k.
 references: 1963, Am. Zoologist 3: 33-56.
 genetics: Gives transvection effect in T(2;3)P23,
  Ubx/bx[34e] heterozygote.
#
T(2;3)P32
 cytology: T(2;3)42D-E;89D7-E1 + Df(2)41A;44C-D.
 new order:: 21 - 41A|44D - 60;
  61 - 89D7|42D - 41A|44C - 42E|89E1 - 100.
 origin: X ray induced in bx[34e].
 discoverer: E. B. Lewis, 50i.
 genetics: Gives transvection effect in T(2;3)P32,
  bx[34e]/Ubx heterozygote. The segregant
  Dp(2;3)P32 = Dp(2;3)41A;42D-E;44C-D;89D7-E1
  survives and is fertile and virtually wild type;
  duplicated for stw, ap, tuf, and cn but not
  pr or ltd.
#
T(2;3)Pu: Translocation (2;3) Punch
 cytology: T(2;3)40F;41A1;70D-E + T(2;3)57B5-C1;79F.
 new order:: 21 - 40F|70E - 79F|57C1 - 60;
  61 - 70D|41A1 - 57B5|79F - 100.
  Tentative.
 origin: X ray induced.
 discoverer: Oliver, 28k4.
 references: Muller, 1930, J. Genet. 22: 326.
  Oliver, 1932, Z. Induktive Abstammungs-
  Vererbungslehre 61: 484.
 genetics: Associated with Pu. Homozygous lethal.
#
T(2;3)Pu[Gr]: Translocation (2;3) Punch-Grape
 cytology: T(2;3)57C;81F (Lewis, 1956, DIS 30: 130).
 origin: X ray induced.
 discoverer: Muller, 29l.
 synonym: T(2;3)Gr: Translocation (2;3) Grape;
  T(2;3)p[Gr]: Translocation (2;3) pink-Grape.
 references: Glass, 1933, J. Genet. 28: 69-112.
  1934, Am. Naturalist 68: 107-14.
 genetics: Mutant for Pu. Homozygous lethal.
#
T(2;3)Pu[rv]: Translocation (2;3) Punch-reversed
 cytology: T(2;3)40F-41A;70D-E + T(2;3)57B5-C1;79F.
 new order:: 21 - 40F|70E - 79F|57B5 - 41A1|70D - 61;
  60 - 57C1|79F - 100.
  Tentative.
 origin: X-ray-induced derivative of T(2;3)Pu =
  T(2;3)40F-41A;70D-E + T(2;3)57B5-C1;79F.
 discoverer: Oliver, 32l27.
 references: 1939, Genetics 24: 82.
  1941, Proc. Intern. Congr. Genet., 7th., p. 228.
 genetics: Partial reversal of Pu. Homozygous lethal.
#
T(2;3)Pu[W]: Translocation (2;3) Punch-Wine
 cytology: T(2;3)57B-C;80.
 origin: X ray induced.
 discoverer: E. B. Lewis, 55h.
 genetics: Mutant for Pu.
#
T(2;3)rn: Translocation (2;3) rotund
 origin: Probably x ray induced.
 discoverer: Glass, 1929.
 references: 1934, DIS 2: 8.
  Muller, 1953, DIS 27: 106-7.
  Carlson, 1956, DIS 30: 109.
 genetics: Mutant for rn. Homozygous viable and sterile in
  both sexes. Breakpoints near the centromeres and
  probably in right arms of chromosomes 2 and
  3 (Carlson, 1956). About 10% of the progeny of
  parents heterozygous for T(2;3)rn and
  chromosome 2 inversions are nondisjunctional
  for chromosome 2 x ller, 1953).
#
T(2;3)S[L]: Translocation (2;3) Star of Lewis
 cytology: T(2;3)21E2-3;81F;88D6-8.
 new order:: 21 - 21E2|81F - 88D6|81F - 61;
  60 - 21E3|88D8 - 100.
  Tentative.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 137-66.
 genetics: Mutant for S.
#
T(2;3)S[M]: Translocation (2;3) Star of Muller
 cytology: T(2;3)21E2-3;79D2-E1 superimposed on
  In(2L)22D1-2;33F5-34A1 + In(2R)42A2-3;58A4-B1.
 new order:: 21A - 21E2|79E1 - 100F;
  60F - 58B1|42A3 - 58A4|42A2 - 34A1|22D2
  - 33F5|22D1 - 21E3|79D2 - 61A.
 origin: X ray induced in In(2L)Cy + In(2R)Cy.
 discoverer: Muller, 1928.
 references: Painter and Muller, 1929, J. Heredity 20: 287-98.
  Muller, 1930, J. Genet. 22: 335-57.
  Morgan, Bridges, and Schultz, 1936, Carnegie
  Inst. Wash. Year Book 35: 293.
 genetics: Mutant for S; also carries Cy.
#
T(2;3)Sa: Translocation (2;3) Salmon
 origin: X ray induced.
 discoverer: Van Atta, 30k1.
 references: 1932, Am. Naturalist 66: 93-95.
  1932, Genetics 17: 637-59.
 genetics: Associated with Sa. Homozygous lethal. Break
  in 2L between pr and centromere and in
  3L near centromere.
#
T(2;3)Sb[V]: Translocation (2;3) Stubble-Variegated
 cytology: T(2;3)41A-C;88;89B superimposed on
  In(3R)93D7-E1;98F2-6. In(3LR)65;83 induced
  simultaneously but was separated from it by
  recombination.
 new order:: 21 - 41A|89B - 93D7|98F2 - 93E1|98F6 - 100;
  61A - 88|89B - 88|41C - 60.
 origin: X ray induced in In(3R)Mo, Sb sr.
 discoverer: E. B. Lewis, 1948.
 references: 1956, DIS 30: 76-77.
 genetics: Variegates for phenotype of deficiency for Sb,
  which is normal.
#
T(2;3)sbd[106]: Translocation (2;3) stubbloid
 cytology: T(2;3)22E;89B.
 origin: X ray induced.
 discoverer: E. B. Lewis.
#
T(2;3)Scar: Translocation (2;3) Scarred
 cytology: T(2;3)27E;95A + In(3)91F;96A.
 new order:: 21 - 27E|95A - 96A|91F - 61;
  60 - 27E|95A - 91F|96A - 100.
 origin: X ray induced.
 discoverer: Yu, 48h.
 references: 1949, DIS 23: 65.
 genetics: Associated with Scar.
#
T(2;3)SM2: Translocation (2;3) Second Multiple
 cytology: T(2;3)21A;40F;80-81 superimposed on
  In(2L)22D1-2;33F5-34A1 + In(2LR)22A3-B1;60B-C +
  In(2R)42A2-3;58A4-B1; position of breaks in
  proximal heterochromatin with respect to centromeres
  not determined.
 origin: X ray induced in In(2LR)SM1.
 discoverer: R. F. Grell, 1953.
 references: Lewis and Mislove, 1953, DIS 27: 58.
  Mislove and Lewis, 1954, DIS 28: 77.
 genetics: Variegated for lt.
 genetics: Discarded because the T(2;3) impairs its general
  usefulness as a chromosome 2 balancer,
  described as SM2 (see Balancers in
  Special Special
  Chromosomes Chromosomes section).
#
T(2;3)sr[4.2]: Translocation (2;3) stripe
 cytology: T(2;3)30C;90C-96.
 origin: X ray induced.
 discoverer: Alexander.
 references: 1960, Genetics 45: 1019-22.
 genetics: Mutant for sr. Homozygous lethal.
#
T(2;3)sr[100.312]
 cytology: T(2;3)40-41;90D2-E1.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for sr. Homozygous lethal.
#
T(2;3)st[100.359]: Translocation (2;3) scarlet
 cytology: T(2;3)21C3-5;73A2-3;98F2-4.
 new order:: 21A - 21C3|73A3 - 98F2|73A2 - 61;
  60 - 21C5|98F4 - 100.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for st. Homozygous lethal.
#
T(2;3;4)+3
 cytology: T(2;3)21D;74F + T(3;4)67C;101E +
  T(3;4)95D-E;97C;101E.
 new order:: 21A - 21D|74F - 95D|97C - 100;
  60 - 21D|74F - 67C|101E - 102F;
  61 - 67C|101E - 101A;
  101A - 101E|95E - 97C|101E - 102F.
  This new order postulates involvement of two fourth
  chromosomes, but the true origin of the centromere
  to which 95E-97C is attached is unknown. In larval
  ganglial metaphases, this element is not visible.
 origin: X ray induced.
 discoverer: Stern, Schaffer, and Heidenthal.
 synonym: R[3](+).
 references: 1946, Proc. Natl. Acad. Sci. U.S. 32: 26-33.
  Stern, MacKnight, and Kodani, 1946, Genetics 31: 598-619.
  Kodani and Stern, 1946, Science 104: 620-21 (fig.).
 genetics: Variegates for ci. Homozygous lethal.
  T(2;3;4)+3/ci has greater interruption of wing
  veins than ci/ci. T(2;3;4)+3/M(4) is normal,
  supporting the postulated involvement of two fourth
  chromosomes.
#
T(2;3;4)bw[R58] Translocation (2;3;4) brown-Rearranged
 cytology: T(2;3;4)59D;65;101C.
 new order:: 21 - 59D|65 - 61;
  60 - 59D|101C - 102;
  ?|65 - 100.
  101A to C lost.
 origin: X ray induced.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R58].
#
T(2;3;4)bw[V30k18] Translocation (2;3;4) brown-Variegated
 origin: X ray induced.
 discoverer: Van Atta, 30k13.
 references: 1932, Genetics 17: 637-59.
 genetics: Variegated for bw. Produces aneuploids that
  have Minute bristles.
#
T(2;4)a
 cytology: T(2;4)50B2-3;102E (E. B. Lewis).
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1931, Genetics 16: 629-58.
 genetics: Homozygous lethal. Fly hyperploid for 2R[D]4[P]
  element rarely survives and is sterile.
#
T(2;4)A6: Translocation (2;4) from Austin
 cytology: T(2;4)57F2-3; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Patterson, Brown, and Stone, 1940, Texas
  Univ. Publ. 4032: 167-89.
 genetics: Homozygous viable and sterile. Fly hyperploid for
  the 4[P]2R[D] element viable and fertile.
#
T(2;4)A8
 cytology: T(2;4)26F4-27A1; breakpoint in
  chromosome 4 not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Patterson, Brown, and Stone, Texas Univ. Publ. 4032: 167-89.
 genetics: Homozygous viable and fertile. Fly hyperploid for
  the 2L[D]4[P] element viable and fertile.
#
T(2;4)A23
 cytology: T(2;4)58F; breakpoint in chromosome 4 not
  determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
 genetics: Homozygous viable and sterile.
#
T(2;4)A27
 cytology: T(2;4)40D1-F1; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
  Patterson, Brown, and Stone, 1940, Texas
  Univ. Publ. 4032: 157-63.
 genetics: Homozygous lethal.
#
T(2;4)A29
 cytology: T(2;4)47A4-5; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Patterson, Brown, and Stone, 1940, Texas
  Univ. Publ. 4032: 167-89.
 genetics: Homozygous lethal.
#
T(2;4)A30
 cytology: T(2;4)53B2-C1; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
  Patterson, Brown, and Stone, 1940, Texas
  Univ. Publ. 4032: 167-89.
 genetics: Homozygous viable and fertile.
#
T(2;4)A34
 cytology: T(2;4)56F6-7; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
  Patterson, Brown, and Stone, 1940, Texas Univ. Publ. 4032: 167-89.
 genetics: Homozygous viable. Either acts as or carries a
  dominant suppressor of Pu (Oliver, 1943,
  Anat. Record 87: 461).
#
T(2;4)A35
 cytology: T(2;4)26E; breakpoint in chromosome 4 not
  determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
 genetics: Homozygous viable.
#
T(2;4)A40
 cytology: T(2;4)49F3-50A1; breakpoint in
  chromosome 4 not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
  Patterson, Brown, and Stone, 1940, Texas
  Univ. Publ. 4032: 167-89.
 genetics: Homozygous viable and fertile.
#
T(2;4)A43
 cytology: T(2;4)22C; breakpoint in chromosome 4 not
  determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Patterson, Brown, and Stone, 1940, Texas
  Univ. Publ. 4032: 167-89.
 genetics: Homozygous viable and fertile. 2L[D]4[P]
  element not recoverable in hyperploid; therefore,
  translocation probably more complex than given.
#
T(2;4)A45
 cytology: T(2;4)36D; breakpoint in chromosome 4 not
  determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
 genetics: Homozygous lethal according to Patterson, Stone,
  Bedichek, and Suche (1934); viable and fertile
  according to Bridges and Brehme (1944,
  Carnegie Inst. Wash. Publ. No. 552: 202).
#
T(2;4)A52
 cytology: T(2;4)36B; breakpoint in chromosome 4 not
  determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
 genetics: Homozygous viable and fertile.
#
T(2;4)A53
 cytology: T(2;4)36E1-3; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-59.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
  Patterson, Brown, and Stone, 1940, Texas Univ. Publ. 4032: 167-89.
 genetics: Homozygous viable and fertile.
#
T(2;4)ast[v] Translocation (2;4) asteroid-variegated
 cytology: T(2;4)21E2-3;101.
 origin: X ray induced.
 discoverer: E. B. Lewis, 1940.
 references: 1945, Genetics 30: 137-166.
 genetics: Variegates for S, ast, and ci. Homozygous
  lethal. Fly with 4[D]2[P] element in place of
  one chromosome 2 survives and has extremely
  rough eyes. 4[D]2[P] is deficient for
  l(2)gl and net and presumably for al, ex,
  and ds. Fly hyperploid for complementary
  2L[D]4[P] also survives.
#
T(2;4)b
 cytology: T(2;4)25E;102C15-D1 (Schultz and E. B. Lewis).
  Metaphase chromosome 4 twice normal size.
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1931, Genetics 16: 629-58.
 genetics: ci not affected. Homozygous viable and fertile.
  Fly hyperploid for 2L[D]4[P] element survives;
  short and thick with flattened abdomen, bulging
  eyes, and curved wings; both sexes sterile.
  Duplicated for M(2)z and dp but not cl,
  ey, or sv (Morgan, 1946, DIS 20: 88).
#
T(2;4)bw[R25] Translocation (2;4) brown-Rearranged
 cytology: T(2;4)59D;101E.
 origin: X-ray-induced derivative of bw.
 discoverer: Slatis.
 references: 1955, Genetics 40: 5-23.
 genetics: Associated with bw[R25].
#
T(2;4)c
 cytology: Metaphase chromosome 4 about twice normal size.
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1961, Genetics 16: 629-58.
 genetics: Homozygote nearly lethal; wings do not expand;
  fly dies early. Break in 2L between dp and
  b, close to dp. Male hyperploid for
  2L[D]4[P] element poorly viable and sterile. No
  variegation for ci[+] (Stern).
#
T(2;4)d
 cytology: T(2;4)55E-F (Lewis, 1956, DIS 30: 130);
  breakpoint in chromosome 4 not determined.
 origin: X ray induced.
 discoverer: Dobzhansky, 1929.
 references: 1930, Biol. Zentr. 50: 671-85.
  1931, Genetics 16: 629-58.
 genetics: Homozygote nearly lethal; fly is short lived and has
  inflated wings. No viable aneuploid product.
#
T(3;4)85C
 cytology: T(3;4)85C; breakpoint in chromosome 4 not
  determined.
 discoverer: E. B. Lewis.
 references: Pipkin, 1959, Texas Univ. Publ. 5914: 69-88.
#
T(3;4)86D
 cytology: T(3;4)86D2-3;101F.
 origin: Neutron induced in bx[34e] e[4].
 discoverer: E. B. Lewis.
 references: Grell, 1959, Genetics 44: 421-35.
  1959, Genetics 44: 911-22.
 genetics: Homozygous viable and fertile. T(3;4)86D/ci has
  ci effect, is enhanced by low temperature, and
  tends to be suppressed by extra Y chromosome. Venation
  of homozygote and haplo-4 is ci[+].
#
T(3;4)88B
 cytology: T(3;4)88B; breakpoint in 4 not determined.
 origin: X ray induced in Ubx.
 discoverer: E. B. Lewis.
 references: Grell, 1959, Genetics 44: 421-35.
 genetics: Homozygous lethal. Has no position effect on ci.
#
T(3;4)89E
 cytology: T(3;4)89E2-3;101F.
 origin: X ray induced in ss bx Su(ss)[2].
 discoverer: E. B. Lewis.
 references: Grell, 1959, Genetics 44: 911-22.
 genetics: Associated with bxd[101]. Homozygous lethal.
  T(3;4)89E/ci has a ci effect, is enhanced by
  low temperature, and tends to be suppressed by extra
  Y chromosome.
#
T(3;4)684
 cytology: T(3;4)67;101; breakpoints roughly estimated
  from figure of Dubinin and Sidorov (1935).
 origin: X ray induced.
 discoverer: Dubinin and Sidorov.
 references: 1934, Biol. Zh. (Moscow) 3: 307-31.
  1935, Biol. Zh. (Moscow) 4: 555-68 (fig.).
 genetics: Position effects on both h and ci.
#
T(3;4)a
 cytology: Metaphase chromosome 4 about one-half length of
  3L.
 origin: X ray induced.
 discoverer: Dobzhansky, 29h.
 references: 1929, Biol. Zentr. 49: 408-19.
  1929, Proc. Natl. Acad. Sci. U.S. 15: 633-38.
  1930, Genetics 15: 347-99.
 genetics: Homozygous lethal. Break in 3L between D and
  th.
#
T(3;4)A1: Translocation (3;4) from Austin
 cytology: T(3;4)89A6-B1;102B; breakpoint in
  chromosome 4 inferred from fig. 40 of
  Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous viable and fertile according to
  Patterson, Stone, Bedichek, and Suche (1934);
  homozygous lethal according to Bridges and Brehme
  (1944, Carnegie Inst. Wash. Publ. No. 552: 203).
#
T(3;4)A2
 cytology: T(3;4)94A3-4;101F |own).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 11-64.
 genetics: Homozygous viable and fertile. Fly hyperploid for
  3R[D]4[P] element survives.
#
T(3;4)A3
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 synonym: T(3;4)A60.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal. 3R broken between e and
  ca.
#
T(3;4)A4
 cytology: T(3;4)80-81;101.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal.
#
T(3;4)A5
 cytology: T(3;4)92A5-6; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
 genetics: Homozygous lethal.
#
T(3;4)A8
 cytology: T(3;4)75B4-5;102D1-3 |own).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 11-64.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
 genetics: Homozygous viable and fertile.
#
T(3;4)A9
 cytology: T(3;4)87E3-F1;102F.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 10: 301-26 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 11-64.
 genetics: Homozygous viable and fertile.
#
T(3;4)A12
 cytology: T(3;4)73C1-2;102C; breakpoint in
  chromosome 4 roughly estimated from fig. 15
  of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
  Pipkin, 1959, Texas Univ. Publ. 5914: 69-88.
 genetics: Homozygote poorly viable and fertile. Fly hyperploid
  for 3L[D]4[P] element survives.
#
T(3;4)A13
 cytology: T(3;4)67E3-4;102D-E; breakpoint in
  chromosome 4 roughly estimated from
  fig. 14 of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedicheck, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Patterson, Brown, and Stone, 1940, Texas
  Univ. Publ. 4032: 167-89.
  Pipkin, 1959, Texas Univ. Publ. 5914: 69-88.
 genetics: Homozygous lethal. Fly hyperploid for 3L[D]4[P]
  element survives.
#
T(3;4)A14
 cytology: T(3;4)80;101.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
#
T(3;4)A20
 cytology: T(3;4)89A;101F; breakpoint in chromosome 4
  roughly estimated from fig. 41 of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal.
#
T(3;4)A22
 cytology: T(3;4)61E-F;102B-C; estimated from fig. 11 of
  Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  1935, Painter, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal. 3L broken to the left of
  ru.
#
T(3;4)A23
 cytology: T(3;4)66D5-E1;101F.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal in male, viable in female.
#
T(3;4)A24
 cytology: T(3;4)99;102B-C; inferred from
  fig. 48 of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous viable and fertile.
#
T(3;4)A27
 cytology: T(3;4)82B3-C1;101A-D.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 11-64.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
 genetics: Homozygous viable and fertile.
#
T(3;4)A28
 cytology: T(3;4)94D3-4;102 (E. B. Lewis); breakpoint in
  chromosome 4 estimated from fig. 44
  of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Pipkin, 1959, Texas Univ. Publ. 5914: 69-88.
 genetics: Homozygous viable and fertile.
#
T(3;4)A30
 cytology: T(3;4)96E5-F1;102B-C; breakpoint in
  chromosome 4 roughly estimated from
  fig. 47 of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Pipkin, 1959, Texas Univ. Publ. 5914: 69-88.
 genetics: Homozygous lethal. Fly hyperploid for 3R[D]4[P]
  survives.
#
T(3;4)A31
 cytology: T(3;4)80;101.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 11-64
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
 genetics: Homozygous viable and fertile.
#
T(3;4)A34
 cytology: T(3;4)61F;101F; estimated from
  fig. 10 of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal. 3L broken to left of ru.
#
T(3;4)A36
 cytology: T(3;4)80B3-C1;102E |own). 3L broken about
  one-sixth the distance from centromere to tip in
  metaphase chromosome.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 10: 301-26 (fig.).
  Brown, 1940, Texas Univ. Publ. 4032: 11-64.
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
 genetics: Homozygous viable and fertile.
#
T(3;4)A37
 cytology: T(3;4)86E5-6;101F; breakpoint in chromosome 4
  roughly estimated from fig. 38 of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal.
#
T(3;4)A39
 cytology: T(3;4)94B4-C1;101F; breakpoint in
  chromosome 4 estimated from fig. 46
  of Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
  Burdette, 1940, Texas Univ. Publ. 4032: 157-63.
 genetics: Homozygous lethal.
#
T(3;4)A43
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal. 3R broken near sr.
#
T(3;4)A44
 cytology: T(3;4)76;99;102D-F; estimated from
  figs. 49 and 51 of Painter (1935).
 new order:: 61 - 76|102D - 101;
  100 - 99|76 - 99|102F.
 references: 1934, Am. Naturalist 68: 359-69.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal.
#
T(3;4)A45
 cytology: T(3;4)80;101.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 phenotype: Homozygous viable and sterile.
#
T(3;4)A52
 cytology: T(3;4)65D3-F2; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 359-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 phenotype: Homozygous viable and fertile.
#
T(3;4)A56
 cytology: T(3;4)76E2-F3;101F; breakpoint in
  chromosome 4 estimated from fig. 17 of
  Painter (1935).
 origin: X ray induced.
 discoverer: Patterson, Stone, Bedichek, and Suche.
 references: 1934, Am. Naturalist 68: 356-69.
  Painter, 1935, Genetics 20: 301-26 (fig.).
 genetics: Homozygous lethal.
#
T(3;4)b
 cytology: Chromosome 4 increased to one-half the length
  of 3L in metaphase figures.
 origin: X ray induced.
 discoverer: Dobzhanksy, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  1929, Proc. Natl. Acad. Sci. U.S. 15: 633-38.
  1930, Genetics 15: 347-99.
 genetics: Breakpoint in 3L near th. Crossing over
  markedly lowered near th and somewhat so at
  3L tip.
#
T(3;4)c
 cytology: T(3;4)86B-C;101F (Lewis, 1951, DIS 25: 108-9).
 origin: X ray induced.
 discoverer: Dobzhansky, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  1929, Proc. Natl. Acad. Sci. U.S. 15: 633-38.
  1930, Genetics 15: 347-99.
 genetics: Homozygous viable and fertile. ci not affected.
  Crossing over much reduced near breakpoint in
  heterozygote and even more reduced in homozygote in
  some regions (Beadle, 1932,
  Proc. Natl. Acad. Sci. U.S. 18: 160-65).
#
T(3;4)d
 cytology: Metaphase figures show barely detectable increase in
  size of chromosome 4.
 origin: X ray induced.
 discoverer: Dobzhansky, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  1929, Proc. Natl. Acad. Sci. U.S. 15: 633-38.
  1930, Genetics 15: 347-99.
 genetics: Homozygous lethal. ci not affected (Stern).
  Breakpoint in 3R between ca and M(3)g and
  in 4 to the left of M(4) and ey.
  Apparently, 4[D]3[P] element can substitute for
  a normal 3, producing Minute flies. Hyperploids
  for 3R[D]4[P] element probably also survive.
#
T(3;4)Dl[7P] Translocation (3;4) Delta-7 of Panshin
 origin: X ray induced.
 discoverer: Panshin.
 references: 1935, Dolk. Akad. Nauk SSSR 4: 85-88.
 genetics: Chromosome 3 broken to the right of cu.
  Mutant for Dl; position effect that weakens
  dominance of cu[+].
#
T(3;4)e
 cytology: T(3;4)79E;102F (Lewis, 1956, DIS 30: 130).
 origin: X ray induced.
 discoverer: Dobzhansky, 28h.
 references: 1929, Biol. Zentr. 49: 408-19.
  1929, Proc. Natl. Acad. Sci. U.S. 15: 633-38.
  1930, Genetics 15: 347-99.
 genetics: Homozygous semilethal and female sterile. ci not
  affected (Stern). Crossing over normal in
  heterozygote except near p.
#
T(3;4)f
 cytology: T(3;4)65D; at least seven bands of
  chromosome 4 inserted into 3L (Lewis, 1956, DIS
  30: 130).
 origin: X ray induced.
 discoverer: Sturtevant, 1930.
 synonym: T(3;4)104.
 references: Beadle, 1933, Z. Induktive Abstammungs-
  Vererbungslehre 65: 111-28.
 genetics: Homozygous lethal. No ci variegation (Stern).
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T(3;4)H1 Translocation (3;4) from Howard University
 cytology: T(3;4)80-81; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Pipkin.
 references: 1959, Texas Univ. Publ. 5914: 69-88.
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T(3;4)H3
 cytology: T(3;4)80-81; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Pipkin.
 references: 1959, Texas Univ. Publ. 5914: 69-88.
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T(3;4)H5
 cytology: T(3;4)96E; breakpoint in chromosome 4 not
  determined.
 origin: X ray induced.
 discoverer: Pipkin.
 references: 1959, Texas Univ. Publ. 5914: 69-88.
 genetics: Fly hyperploid for 3R[D]4[P] survives.
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T(3;4)H6
 cytology: T(3;4)98A; breakpoint in chromosome 4
  not determined.
 origin: X ray induced.
 discoverer: Pipkin.
 references: 1959, Texas Univ. Publ. 5914: 69-88.
 genetics: Fly hyperploid for 3R[D]4[P] survives.
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T(3;4)H7
 cytology: T(3;4)66C; breakpoint in chromosome 4 not
  determined.
 origin: X ray induced.
 discoverer: Pipkin.
 references: 1959, Texas Univ. Publ. 5914: 69-88.
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T(3;4)K: Translocation (3;4) of Kirssanov
 origin: X ray induced.
 discoverer: Kirssanov.
 references: 1933, Biol. Zh. (Moscow) 2: 447-50.
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T(3;4)l-18: Translocation (3;4) lethal
 origin: X ray induced.
 discoverer: Gloor and Green, 1957.
 genetics: Variegates for ci; mutant for l(4)18.
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T(3;4)P86: Translocation (3;4) from Pasadena
 cytology: T(3;4)88B-C;101 (E. B. Lewis).
 origin: X ray induced.
 discoverer: E. B. Lewis.
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Tp(1)B[263-48]: Transposition (1) Bar
 cytology: Tp(1)3E2-3;15F9-16A1;20A2-3.
 new order:: 1 - 3E2|16A1 - 20A2|3E3 -
  15F9|20A3 - 20F.
 origin: X ray induced.
 discoverer: Bishop, 1939.
 references: Sutton, 1943, Genetics 28: 99.
 genetics: Male and homozygous female viable. Crossing over in
  region 3E3-15F9 in Tp(1)B[263-48]/+ heterozygote
  yields Dp(1;1)B[263-48] =
  Dp(1;1)3E2-3;15F9-16A1;20A2-3, which is
  heterozygous viable and produces the Bar effect. The
  complementary deficiency is heterozygous lethal.
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Tp(1)ct[6a1]: Transposition (1) cut
 cytology: Tp(1)7B2-C1;19;20.
 new order:: 1 - 7B2|(19 - 20)|7C1 - 19|20.
  Nucleolus organizer included in transposed piece.
 origin: X ray induced.
 discoverer: Hannah, 1947.
 references: 1949, Proc. Intern. Congr. Genet., 8th., pp. 588-89.
 genetics: Variegated for ct. Male lethal.
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Tp(1)N[264-63]: Transposition (1) Notch
 cytology: Tp(1)3C7-9;13C7-8;19F (Hoover).
 new order:: 1 - 3C7|(13C8 - 19F)|(3C9 -
  13C7)|19F - 20.
 origin: X ray induced.
 discoverer: Demerec, 38e.
 genetics: Mutant for N but not for w, rst, or dm.
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Tp(3)bxd[100]: Transposition (3) bithoraxoid
 cytology: Tp(3)66C;89B5-6;89E2-3.
 new order:: 61 - 66C|(89B6 - 89E2)|66C -
  89B5|89E3 - 100.
 origin: X ray induced.
 discoverer: E. B. Lewis.
 references: 1951, Cold Spring Harbor Symp. Quant. Biol. 16: 159-74.
 genetics: Mutant for bxd but not bx. Dp(3;3)bxd[100] =
  Dp(3;3)66C;89B5-6;89E2-3, which is derived by crossing over
  in region 66C-89B of Tp(3)bxd[100]/+, survives
  and is duplicated for bx and lethal effect of
  Ubx but not for bxd. The complementary
  Df(3R)bxd[100] = Df(3R)89B5-6;89E2-3 survives in
  heterozygote and has Ubx phenotype.
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Tp(3)bxd[110]
 cytology: Tp(3)89E2-3;91C7-D1;92A2-3.
 new order:: 61 - 89E2|(91D1 - 92A2)|89E3 -
  91C7|92A3 - 100.
 origin: X ray induced.
 discoverer: E. B. Lewis.
 genetics: Mutant for bxd but not bx or Dl.
  Df(3R)bxd[110] = Df(3R)91C7-D1;92A2-3, derived
  from crossing over in region 89E-91C in
  Tp(3)bxd[110]/+ female, survives in heterozygote
  and has Dl phenotype. The complementary
  Dp(3;3)bxd[110] = Dp(3;3)89E2-3;91C7-D1;92A2-3
  is duplicated for Dl and acts as a suppressor of
  Dl in Dp(3;3)bxd[110]/Dl[7] heterozygote
  (E. B. Lewis).
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Tp(3)C285 Transposition (3) Crossover suppressor
 cytology: Tp(3)88F;98B;99B.
 new order:: 61 - 88F|98B - 99B|88F - 98B|99B - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous lethal. Recombination between st and
  ca sharply reduced.
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Tp(3)C341
 cytology: Tp(3)63C;71E;80-81 position of right breakpoint
  in chromosome 3 with respect to centromere not
  determined.
 new order:: 61 - 63C|71E - 80|(63C - 71E)|81 - 100.
 origin: X ray induced.
 discoverer: Roberts, 1965.
 genetics: Homozygous viable. Recombination reduced in 3L.
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Tp(3)sr[300.240]: Transposition (3) stripe
 cytology: Tp(3)75C;89E;92A.
 new order:: 61 - 75C|(89E - 92A)|75C - 89E|92A - 100.
  Inserted piece said to be in inverted order but not
  specified whether with respect to numerical sequence
  or centromere.
 origin: X ray induced.
 discoverer: Alexander.
 references: Ward and Alexander, 1957, Genetics 42: 42-54.
 genetics: Mutant for sr. Homozygous lethal.
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Tp(3)Vno: Transposition (3) Vein off
 cytology: Tp(3)89E;93F;97A (Nicoletti and Lewis, 1960, DIS
  34: 53).
  61 - 89E|93F - 97A|89E - 93F|97A - 100.
 origin: X ray induced.
 discoverer: E. H. Grell, 56c.
 synonym: In(3R)Vno.
 references: 1959, DIS 33: 94.
 genetics: Associated with Vno. Homozygous lethal.
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