# T(Y;2) - T(Y;2;3) Table I: T(Y;2)a2-T(Y;2;3)rc77 origin: / ray induced. discoverer: Lyttle. synonym: T(Y;2)A2-T(Y;2)RC77. genetics: Male fertile with normal X. new break Df(1)bb158/T(Y;2) translocation cytology order ( in | male fertility ____________________________________________________________________________ T(Y;2)a2 /`- h11-h13;41A-B 4 - T(Y;2)a15 BSYy+;35A4-B1 1b T(Y;2)a18 BSYy+;36B 1b T(Y;2)a21 BSYy+;36B-C 1b T(Y;2)a35 BSYy+;35C-E 1b T(Y;2)a38 BSYy+;35B-40 1c T(Y;2)b6 Ybbl;35B-D 7 T(Y;2)b8 Ybbl;35C1-D1 T(Y;2)b10 ` YL;36D2-3 1 T(Y;2)b12 30F 1 T(Y;2)b13 ` YS;57A 1 T(Y;2)b14 41B-C 1 T(Y;2)b15 24C-D 1 T(Y;2)b20 YS;40-41;47B 1 1 T(Y;2)b23 YS;42A;60A-B 2 1 T(Y;2)b24 Y;36C + 40E--F;44B 3 1 T(Y;2)c5 ` 38B1-2 4 T(Y;2)c79 BSYy+;35A 4b T(Y;2)cb2 YS;27C;36F 5 +(semi) T(Y;2)cb3 YL;30F 5 - T(Y;2)cb4 30B 5 - T(Y;2)cb5 `- h25;41 5 - T(Y;2)cb6 40-41 5 - T(Y;2)cb7 40-41 5 - T(Y;2)cb8 57C-D 5 - T(Y;2)cb9 35F 5 - T(Y;2)cb10 35E 5 - T(Y;2)cb11 YL;55B 5 - T(Y;2)cb13 36A7-10 5 - T(Y;2)cb14 distal to B on YL; 5 + distal to all bands on 2L or 2R T(Y;2)cb16 - h9-h10; distal to all 5 + bands on 2L or 2R T(Y;2)cb18 36D-E 5 - T(Y;2)cb21 55F 5 - T(Y;2)cb22 34D 5 - *T(Y;2)cb23 24C;60A;88F 5 T(Y;2)cb24 35A-B 5 - T(Y;2)cb25 YL (in B marker); 5 - 41A (prox. to all Hoechst S33258 bands) T(Y;2)cb31 40-41 5 - T(Y;2)cb34 40-41 5 - T(Y;2)cb36 34A 5 - T(Y;2)cb37 33F 5 - T(Y;2)cb38 25D 5 - T(Y;2)cb42 42A 5 - T(Y;2)cb44 40-41 5 - T(Y;2)cb48 25A-B;30D-F;55E 4 5 - T(Y;2)da4 40-41 4 T(Y;2)da5 40-41 4 T(Y;2)da6 40-41 4 T(Y;2)e2 Ybbl;35D1-4;35E1-2 7 T(Y;2)e24 Ybbl;36B-C T(Y;2)l1 59C 3 T(Y;2)m1 25D-E;56B-C 4 T(Y;2)m3 40-41 + 2a In(2L)27A;38A T(Y;2)ra6 48B-C 1b - T(Y;2)ra8 YL;40B-F 1b - T(Y;2)ra18 36B 1b - T(Y;2)ra23 55C-E 1b - T(Y;2)ra35 35C-E 1b - T(Y;2)ra46 48E 1b + T(Y;2)ra55 YS;21F 1b + T(Y;2)rb9 25F 1b T(Y;2)rc5 YL;38B1-2 4a - T(Y;2)rc22 40-41 4a + T(Y;2)rc30 24F 4a - T(Y;2)rc43 YS;40-41 4a - T(Y;2)rc45 28C5-9 4a - T(Y;2)rc52 29F 4a +(semi) T(Y;2)rc58 38A 4a - T(Y;2)rc71 36B-C 4a - T(Y;2)rd4 37C-D 1b +(semi) T(Y;2)re4 21C 1b T(Y;2)re14 40-41 1b + In(2L)34D;37F T(Y;2)re21 40-41 1b T(Y;2)re32 42F 1b T(Y;2)re39 49A 1b T(Y;2)sl4 YS;40A-F 1a (prox. to lt) T(Y;2)t21 40-41 4 - T(Y;2)t22 ` YL;36B-C 4 - T(Y;2)t41 ` 41B-C + In(2L)25A;? 3 T(Y;2;3)b11 42A-B;86A-B;92E 5 1 T(Y;2;3)b21 YS;57B + 24E-F;63A 6 1 T(Y;2;3)b22 40E-F;91F 1 T(Y;2;3)cb15 YL;21A1-3;80B3;87A-B 5 - T(Y;2;3)cb19 28C;40-41;87A6 5 - T(Y;2;3)cb23 24C;60A;88F 5 T(Y;2;3)cb45 Y;44C + 37D;79B 7 5 - T(Y;2;3)cb47 Y;97D + 52D; 8 5 - 55C-D + 42D;86C T(Y;2;3)ra24 38B-C;93B-D 9 1b - T(Y;2;3)ra34 YL;25F;97F 10 1b + T(Y;2;3)rc17 YS;43A-B;62E 4a + T(Y;2;3)rc77 YS;30B;73F-74A + 26CD; 11 4a + 53C-D + 55D-E; 60E-F + 61A;80 ( 1 = YD or P|47B - 41|47B - 60F; YP or D|40 - 21A. 2 = YL.YSP|60A - 42A|60B - 60F; YSD|42A - 21A. 3 = YD|36C - 40E|44B - 40F|44B - 60F; YP|36B - 21A. 4 = YD|55E - 30E|25A - 21A; YP|30D - 25B|55E - 60F. 5 = YD|42A - 21A; YP|86B - 92E|42B - 60F; 61A - 86A|92E - 100F. 6 = YL.YSP|57B - 60F; YSD|57B - 24F|63A - 61A; 21A - 24E|63A - 100F. 7 = YD|44C - 37D|79B - 61A; YP|44C - 60F; 21A - 37D|79B - 100F. 8 = YD|97D - 86C|42D - 21A; YP|97D - 100F; 61A - 86C|42D - 52D|55C - 52D|55C - 60F. 9 = YD|93B - 61A; YP|38B - 21A; 60F - 38C|93D - 100F. 10 = YD|25F - 60F; YP|97F - 100F; 21A - 25F|97F - 61A. 11 = YL.YSP|30B - 26C|53D - 55D|60F; YSD|73F - 61A|80 - 74A|30B - 51F|56E - 55E|60E - 56F|52A - 53C|26D - 21A; 61A|80 - 100F. | 1 = SD-Roma; 1a = SD-Roma carrying In(2LR)SL = In(2LR)21E-F;41; 1b = SD-Roma carrying In(2LR)PuL = In(2LR)40B;57B-C; 1c = SD- Roma carrying In(2LR)Pu + In(2LR)36B;57A5-10; 2 = SD-36; 2a = SD-79; 3 = SD-72; 4 = SD-NH2; 4a = SD-NH2 with In(2LR)DA3 = In(2LR)26D;53E + In(2LR)39D-E;42A + In(2R)52A;56F + In(2R)55E;60; 5 = cn bw (Madison, WI. Stock); 6 = T(Y;2)L141; 7 = Ybbl. / Associated with lace. ` References: Lyttle, 1986, Genetics 114: 203-16 [T(Y;2)b10]; Lyttle, 1984, Genetics 106: 423-34 [T(Y;2)t22]; Lyttle, 1977, Genetics 86: 413-45 [T(Y;2)t41]. - Y breakpoints from Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73. Associated with el5. Table II: T(Y;2)A24-T(Y;2)S14 origin: X ray induced using BSYy+. genetics: Many are male sterile in combination with deficien- cies for Xh. X/T(Y;2) translocation cytology (| ref / male fert. | ____________________________________________________________________________________ T(Y;2)A24 (YS); 46A 3, 5, 9 - *T(Y;2)A33 56F 5, 9 + T(Y;2)A62 BSXh;36C1-2 (Ashburner) 3, 5, 9 + T(Y;2)A77 ` h19;23F;25A 3, 5, 9 + T(Y;2)A80 h21;35A3-4 + Df(YL)BSXh;h7 1, 5, 9 - T(Y;2)A87 YL;40 (or 38A-B) 5, 8, 9 + *T(Y;2)A96 YL;59D + In(3R)65F;80-81 5, 9 + *T(Y;2)A97 34A 5, 9 - T(Y;2)A107 YL;40 5, 8, 9 + T(Y;2)A109 YL;83E 5, 9 + T(Y;2)A111 h14;28D + Df(YL)h5;h11 3, 5, 9 - T(Y;2)A120 ` h16;h21;57E 3, 5, 9 - T(Y;2)A128 YL;40 5, 9 - *T(Y;2)A139 36D-E 5, 9 - T(Y;2)A145 h25;29F 3, 5, 9 + T(Y;2)A146 Xhy+;60F 3, 5, 9 + T(Y;2)A159 YS;40 5, 9 + T(Y;2)A160 YS;60B-C 5, 9 + T(Y;2)A161 Xhy+;21B 3, 5, 9 + T(Y;2)A162 h21;31E-F 3, 5, 9 - T(Y;2)A165 YL;55E-F 5, 9 - T(Y;2)A169 h13;55B 3, 5, 9 + T(Y;2)A171 h3;27D 3, 5, 9 - T(Y;2)A183 48D-E 2 T(Y;2)B3 YS;40-41 4 - T(Y;2)B4 h21;36C(Df) 3, 5, 9 - T(Y;2)B5 YS;21C-D 5, 9 + T(Y;2)B13 22E-F + Df(YL)B13 4 - T(Y;2)B24 h23;43B 3, 5, 9 (+) T(Y;2)B26 BSXh;43E-F 3, 5, 9 (-) T(Y;2)B63 YS;41 5, 9 + T(Y;2)B66 Xhy+;28C 3, 5, 9 (-) T(Y;2)B80 ` Xhy+;h21;60F 3, 5, 9 + T(Y;2)B92 h11;33B 3, 5, 9 (-) T(Y;2)B104 BSXh;28D 3, 5, 9 + *T(Y;2)B106 h21;60B 3, 5, 9 - T(Y;2)B107 `- BSXh;29C;47E 3, 5, 9 + T(Y;2)B110 h3;38C 3, 5, 9 - T(Y;2)B112 h25D;22C 3, 5, 9 + T(Y;2)B135 h23;42A-B 3, 5, 9 - T(Y;2)B137 Xhy+;25D6-7 1, 3, 5, 9 + T(Y;2)B177 YL;41 5, 9 + T(Y;2)B184 h25D;56C 3, 5, 9 (-) T(Y;2)B185 ` YS;60F + 34A;51A;53C-D 5, 9 + T(Y;2)B190 YS;40 (or 39C) 5, 8, 9 + T(Y;2)B196 YS;40 5, 9 + T(Y;2)B199 YL;40 5, 8, 9 - T(Y;2)B202 h20;59A-B 3, 5, 9 + T(Y;2)B209 YL;40 (or 39D-E) 5, 8, 9 - T(Y;2)B210 h25D;36A2-6 (Ashburner) 3, 5, 9 + *T(Y;2)B212 33F-34A 5, 9 T(Y;2)B214 Xhy+;36A2-6 (Ashburner) 3, 5, 9 + T(Y;2)B224 Xhy+;33F-34A 3, 5, 9 + T(Y;2)B228 YS;60F 5, 9 + T(Y;2)B236 BSXh;h16;25D-E(Df) 3, 5, 9 - T(Y;2)B238 YS;41 5, 9 + T(Y;2)B242 h14;36C 3, 5, 9 - T(Y;2)B251 YS;40 (or 39D-E) 5, 8, 9 - T(Y;2)D6 Xhy+;24C3;24C4-6;24E1-2;25D2-3; 1, 3, 5, 9, 10 + 25D6-7 (complex; includes inversion and deficiency in 2L). T(Y;2)D19 h3;48E 3, 5, 9 - T(Y;2)D20 YL;40 5, 9 - T(Y;2)D70 YS;21D 5, 9 + T(Y;2)D106 h21;26B 3, 5, 9 (+) T(Y;2)D110 BSXh;25D1-2 3, 5, 9 (-) T(Y;2)D211 BSXh;h3;26B3-5 3, 5, 9 + (Knipple and MacIntyre, 1984) T(Y;2)D212 YL;33F 5, 9 - T(Y;2)D217 YL;35D 5, 9 - T(Y;2)D219 ` YL;35F-36A;36E-37A 5, 9 - T(Y;2)D222 YS;25F-26A1 5, 9 - T(Y;2)D225 YS;40 5, 9 - T(Y;2)G10 YS;41 5, 9 - T(Y;2)G20 Xhy+;31C-D 3, 5, 9 + T(Y;2)G53 h3;50A 3, 5, 9 - T(Y;2)G74 h7;34C3 1, 3, 5, 9, 11 (kl3--kl5-) T(Y;2)G100 Xhy+;56D 3, 5, 7, 9 + T(Y;2)G105 Xhy+;25F 3, 5, 7, 9 + T(Y;2)G113 YS;40 5, 9 + T(Y;2)G120 h24;24A 1, 3, 5, 9 + T(Y;2)G146 h23;23B-C 1, 3, 5, 9 + T(Y;2)H52 Xhy+;28B4-C1 + 3, 5, 9 (+) Df(YL)h3;h16 T(Y;2)H54 YL;40 (or 39D-E) 5, 8, 9 - T(Y;2)H56 Xhy+;22B 3, 5, 9 (-) T(Y;2)H69 h21;26A7-8 3, 5, 9 - (Knipple and MacIntyre, 1984) T(Y;2)H116 h3;24F5-6 1, 3, 5, 9 - T(Y;2)H118 YL;40 5, 8, 9 + T(Y;2)H121 h16;26B + 3, 5, 9 (+) Df(YL)h3;h13 T(Y;2)H124 YS;40 5, 9 - T(Y;2)H131 YL;40 5, 8, 9 - T(Y;2)H136 h3;44C 3, 5, 9 - T(Y;2)H137 h25;60D 3, 5, 9 + T(Y;2)H143 BSXh;h14;59F; deficient 3, 5, 9 (+) for BSXhj-h13 T(Y;2)H144 h3;47F 3, 5, 9 - T(Y;2)H149 h21;54F 3, 5, 9 - T(Y;2)H151 YS;25F3 5, 9 + T(Y;2)H158 Xhy+;58D 3, 5, 9 + T(Y;2)H164 YS;25E + 5, 9 + In(2)40-41;44F T(Y;2)H165 ` Xhy+;21E;25D 3, 5, 9 + T(Y;2)H174 YS;37D12-E12 (Ashburner) 5, 9 - T(Y;2)J30 YS;40 5, 9 + T(Y;2)J43 YS;41 5, 9 - T(Y;2)J45 YL;40-41;49E 9 + T(Y;2)J59 Xhy+;43A + Df(YL)h3;h16 3, 5, 9 (+) T(Y;2)J69 h21;22A 3, 5, 9 - T(Y;2)J70 h11;26B + In(Y)h3;h21 3, 5, 9 - T(Y;2)J118 h21;22D + Df(YL)h3;h10 1, 3, 5, 9 - T(Y;2)J122 YS;23E1-2 1, 5, 9 - T(Y;2)J131 YL;59D 5, 9 + T(Y;2)J136 BSXh;26F5-7 3, 5, 9 + + Df(YL)h3;h9 T(Y;2)J146 h14;21B 3, 5, 9 + *T(Y;2)J157 YL;60? 5, 9 + T(Y;2)J160 YS;33E-34A 5, 9 + T(Y;2)J163 h23;57F 3, 5, 9 - T(Y;2)J165 h21;35C4-5 1, 3, 5, 9, 11 - T(Y;2)J166 h25D;31D-E 3, 5, 9 + T(Y;2)L11 h25D;60C 3, 5, 9 + T(Y;2)L23 h21;45F 3, 5, 9 - T(Y;2)L26 h25D;24C 3,9 + T(Y;2)L52 h3;30F 3, 5, 9 (+) T(Y;2)L62 Xhy+;56E-F 3, 5, 6, 7, 9 (-) T(Y;2)L67 ` Xhy+;25E;40 3, 5, 9 - T(Y;2)L107 YL;57B 5, 9 - T(Y;2)L110 h3;50C 3, 5, 9 + T(Y;2)L116 Xhy+;58A 3,9 (-) T(Y;2)L124 Xhy+;21C 3, 5, 9 + T(Y;2)L126 YS;40 9 + T(Y;2)L134 YS;40 5, 9 + T(Y;2)L135 ` YS;31F;40 5, 9 - T(Y;2)L137 ` YS;43E;60A 5, 9 + T(Y;2)L138 Xhy+;39C 3, 5, 8, 9 + T(Y;2)L139 n Xhy+;56E 3, 5, 6, 7, 9 + T(Y;2)L140 YL;40 5, 9 - T(Y;2)L141 n Xhy+;56F 3, 5, 6, 7, 9 + T(Y;2)P8 h21;24D 3, 5, 9 - T(Y;2)P42 YS;40 5, 9 + T(Y;2)P51 h21;25D6-7 1, 3, 5, 9 (+) T(Y;2)P57 - h9-10;38B 3, 5, 9 - T(Y;2)P58 Xhy+;35D5-8 1, 3, 5, 9, 11 + T(Y;2)P59 Xhy+;59B 3, 5, 9 + T(Y;2)R9 YS;40 5, 9 + T(Y;2)R14 i h3;53A-B 3, 5, 9 - T(Y;2)R15 Xhy+;35B9-C1 1, 3, 5, 9, 11 + T(Y;2)R50 h1-2;28B 3, 5, 9 - T(Y;2)R85 YS;40 5, 9 - T(Y;2)R93 h21;57A 3, 5, 9 - *T(Y;2)R103 YS;60E-F 5, 9 + T(Y;2)R104 Xhy+;58A 3, 5, 9 + T(Y;2)R116 YL;40 5, 8, 9 + T(Y;2)R123 YL;60F 5, 9 - T(Y;2)R124 h3;55E 3, 5, 9 - T(Y;2)R127 h21;24F-25A 3, 5, 9 - T(Y;2)R131 27E-F 2 T(Y;2)R136 h3;h7;22D; deficient 3, 5, 9 - for h4-h6 T(Y;2)R145 ` YS;23F;40 5, 9 - T(Y;2)R146 YL;40 5, 9 + T(Y;2)R147 ` BSXhj;23;27E 3, 5, 9 + T(Y;2)R155 h10-h11;43C 3, 5, 9 - T(Y;2)R158 Xhy+;32F + Df(YL)BSXhj;h10 3, 5, 9 + *T(Y;2)S14 YL;56F 5, 9 ( Y breakpoints in the terminology of Gatti and Pimpinelli, 1983, whenever available. | Parentheses used for data from Lindsley et al., 1972, that differ from data from Gatti and Pimpinelli, 1983. / 1 = Ashburner and Velissariou, 1980, DIS 55: 196; 2 = Baker, 1980, DIS 55: 197; 3 = Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73; 4 = Hazelrigg, Fornili, and Kaufman, 1982, Chromo- soma 87: 535-59; 5 = Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethmann, Hardy, Hessler, Miller, Nozawa, and Gould-Somero, 1972, Genetics 71: 157-84; 6 = Procunier and Dunn, 1978, Cell 15: 1087-93; 7 = Procunier and Tartof, 1976, Nature 263: 255-57; 8 = Siegel, 1981, DIS 56: 123-24; 9 = The Seattle-La Jolla Drosophila Laboratories, 1971, DIS 47, Suppl.; 10 = Velissariou and Ashburner, 1980, Chromosoma 77: 13-27; 11 = Woodruff and Ashburner, 1972, Genetics 92: 117-32. ` New order: T(Y;2)A77 = BSXh - h19|23F - 25A|23F - 21; Xhy+ - h19|25A - 60. T(Y;2)A120 = BSXh - h16|h21 - h16|57E - 60; Xhy+ - h21|57E - 21. T(Y;2)B80 = BSXh - h21|Xhy+ - h21|60F; Xhy+|60F - 21. T(Y;2)B107 = BSXh|29C - 47E|29C - 21; Xhy+ - BSXh|47E - 60. T(Y;2)B185 = YL.YSP|60F; YSD|60F - 53D|51A - 53C|34A - 51A|34A - 21. T(Y;2)D219 = YLD|36F - 60; YS.YLP|36E - 36A|35F - 21. T(Y;2)H165 = BSXh - Xhy+|21E - 21A; Xhy+|28D - 21E|28D - 60. T(Y;2)L67 = BSXh - Xhy+|25E - 40|25E - 21; Xhy+|40 - 60. T(Y;2)L135 = YLD.YSP|31F - 40|31F - 21; YS|40 - 60. T(Y;2)L137 = YL.YSP|60A - 60F; YSD|43E - 60A|43E - 21. T(Y;2)R145 = YL.YSP|23F - 40|23F - 21; YSD|40 - 60. T(Y;2)R147 = BSXh|27E - 60 YS.YL|23 - 27E;|23 - 21. - Synonym: T(Y;2)Kr. ` Broken within the 5S RNA gene cluster (Procunier and Tartof, 1976; Procunier and Dunn, 1978). n Broken just outside the 5S RNA gene cluster, proximal for T(Y;2)L139 and distal for T(Y;2)L141 (Procunier and Dunn, 1978). Completely male sterile in combination with Df(1)bb158 (Lyttle). - Suppresses Y loop associated with kl-3 (Bonaccorsi and Gatti). i Cytology corrected by Davis and MacIntyre, 1988, Genetics 120: 755-66. . # T(Y;2)1 - T(Y;2)16 origin: X ray induced. references: Novitski and Ehrlich, 1970, DIS 45: 102. translocation cytology induced in _____________________________________ T(Y;2)1 56E Y T(Y;2)7 57D Y T(Y;2)11-11N 34A y+Y T(Y;2)11-26A 36F y+Y T(Y;2)12-4A 34A y+Y T(Y;2)16 59F Y # T(Y;2)2.31 cytology: T(Y;2)25C;38B. new order: YP|25C - 21; YD|38B - 25C|38B - 60. origin: X ray induced. discoverer: Nusslein-Volhard. synonym: T(Y;2)odd2.31. references: Nusslein-Volhard, Kluding, and Jurgens, 1985, Cold Spring Harbor Symp. Quant. Biol. 50: 145-54. genetics: Second-chromosome breakpoint between slp and mid; neither gene mutant. # T(Y;2)4.25 cytology: T(Y;2)24D. origin: X ray induced. discoverer: Nusslein-Volhard. synonym: T(Y;2)odd4.25. references: Nusslein-Volhard, Kluding, and Jurgens, 1985, Cold Spring Harbor Symp. Quant. Biol. 50: 145-54. genetics: Second-chromosome breakpoint between slp and mid; neither gene mutant. #*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 YP2D and 2PYD recoverable in aneuploid pro- geny. #*T(Y;2)54a cytology: T(Y;2)YL;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 YP2D survives, is not variegated, and is sterile. # T(Y;2)60D-F: see In(2LR)noc7 # T(Y;2)429 - T(Y;2)434 origin: X ray induced. discoverer: Gelbart. translocation cytology _________________________________ T(Y;2)429.39 25E-F T(Y;2)434.78 25E1-4 T(Y;2)434.86 27C1-2 T(Y;2)434.89 35D-E T(Y;2)434.105 32A1-4 # 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: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1932, Z. Indukt. Abstamm. Vererbungsl. 60: 235-86. genetics: Break between pr and tk. rl, M(2)41A, 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: Translocation (Y;2) Bar cytology: T(Y;2)40F-41A1; placed in 2R by Whittinghill (1937, DIS 8: 82). Y breakpoint at telomeric end of YS, as indi- cated by fluorescence analysis (Halfer, Tiepolo, Barigozzi, and Fraccaro, 1972, Chromosoma 39: 43-44). origin: X ray induced. discoverer: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1932, Z. Indukt. Abstamm. Vererbungsl. 60: 235-86. genetics: Lethal in combination with Df(2R)M41A10 and shows an extreme rl phenotype with rl. stw, ap, msf, tk, and ltd not affected. # T(Y;2)BSV5: Translocation (Y;2) Bar of Stone Variegated cytology: T(Y;2)YL;41. discoverer: Craymer. # T(Y;2)BSV14 cytology: T(Y;2)YL;80. discoverer: Craymer. # T(Y;2)bwDrv18 cytology: In(2L)59B1-2. references: P. Simpson. #*T(Y;2)bwR27: 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 bwR27. #*T(Y;2)bwR57 cytology: T(Y;2)59D5-6. origin: X ray induced. discoverer: Slatis. references: 1955, Genetics 40: 5-23. genetics: Associated with bwR57. # 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: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1932, Z. Indukt. Abstamm. Vererbungsl. 60: 235-86. genetics: Does not affect rl, M(2)41A, stw, ap, msf, tk, or ltd. # T(Y;2)CA discov induced translocation cytology origin or ref ( with ______________________________________________________________ T(Y;2)CA13 40-41 X ray 2 In(2L)Scorv5 T(Y;2)CA19 60D7-8 / ray 3 In(2LR)noc7 T(Y;2)CA27 34B1-2 / ray 4 T(Y;2)CA42 40-41 / ray 1 Df(2L)TE35A-6 T(Y;2)CA50 24F / ray 1 Df(2L)TE35A-219 ( 1 = Ashburner; 2 = Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95; 3 = Gubb, Roote, Harrington, McGill, Durrant, Shelton, and Ash- burner, Chromosoma 92: 116-23; 4 = Roote. # T(Y;2)CyO: Translocation (Y;2) Curly Oster cytology: Translocation between Y and CyO, l(2)DTS513DTS. Cytology not given. origin: X ray induced. references: Wright and Green, 1974, DIS 51: 108-09. genetics: Cy males carry temperature-sensitive lethal. Useful for constructing virginator stocks. # T(Y;2)D: see T(Y;2;3)D # T(Y;2)dp61d: Translocation (Y;2) dumpy origin: X ray induced. discoverer: Thompson, 61d. genetics: Mutant for dp. #*T(Y;2)dpw2: 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)dpp16: Translocation (Y;2) decapentaplegic cytology: T(Y;2)22F1-2. origin: X ray induced. discoverer: Spencer. references: Gelbart. genetics: d-III dpp mutant. # T(Y;2)DTD50 cytology: T(Y;2)35D-E. discoverer: Gelbart. genetics: Disrupts transvection at dpp. # 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. Indukt. Abstamm. Vererbungsl. 60: 235-86. genetics: Male fertile; Df(1)sc4Lsc8R/T(Y;2)E male is sterile. # T(Y;2)el4: Translocation (Y;2) elbow cytology: T(Y;2)35B1. Y arm not determined. origin: Induced by ethyl methanesulfonate. discoverer: Harrington. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. genetics: Associated with el4. Thought to be mutant, but not deficient, for el since el4/el is like el/el but less extreme than el/Df. #*T(Y;2)Elp2: Translocation (Y;2) Ellipse cytology: T(Y;2)57C9-D5. origin: X ray induced. discoverer: Angel. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. genetics: Ellipse-like eye phenotype; allelism with EgfrE1 not tested before translocation lost. # T(Y;2)enSF32: Translocation (Y;2) engrailed cytology: T(Y;2)48A. origin: X ray induced. references: Kuner, Nakanishi, Ali, Drees, Gustavson, Theis, Kauvar, Kornberg, and O'Farrell, 1985, Cell 42: 309-16. genetics: Mutant for en; a lethal allele. molecular biology: Located at -2 kb on the molecular map of en ("-" values to left, "+" values to right of en which is at position 0). # T(Y;2)F: see T(Y;2;3)F # T(Y;2)GT1 cytology: T(Y;2)35A4-B1. origin: / ray induced. discoverer: Durrant. genetics: Deficient for noc-osp. # T(Y;2)GT2 cytology: T(Y;2)35A1-2. origin: / ray induced. discoverer: Durrant. genetics: Deficient for l(2)35Aa-pu. # T(Y;2)IC68-5 cytology: T(Y;2)41F;53B. new order: YP|53B - 60F; YD|41F - 53B|41F - 21. origin: X ray induced. references: Brosseau, 1969, DIS 44: 45. genetics: Male fertile; shows dominant rough eye phenotype (allelism not determined). # T(Y;2)Jrv99: Translocation (Y;2) Jammed-revertant cytology: {T(Y;2)31B-F}. Autosomal breakpoint assumed to be at or near J. origin: X ray induced in J males. synonym: J-der-99. references: Salas and Lengyel, 1984, DIS 60: 243-44. genetics: Revertant of J. # T(Y;2)J-D: Translocation (Y;2) J of Dobzhansky cytology: T(Y;2)40F-41A1;57F1-2 (Whittinghill, 1937, DIS 8: 82-84). new order: YD or P|40F - 21; YP or D|57F1 - 41A1|57F2 - 60. origin: X ray induced. discoverer: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1932, Z. Indukt. Abstamm. Vererbungsl. 60: 235-86. genetics: Does not affect rl, M(2)41A, stw, ap, msf, tk, or ltd. # T(Y;2)JL11 cytology: T(Y;2)YS;56F + In(2LR)21A;57F. new order: YL.YS|56F - 57F|21A; 60F - 57F|21A - 56F|YSy+. origin: /-ray-induced 2 translocation from T(Y;2)L141 = T(Y;2)56F. references: Mackay and O'Donnell, 1983, Genetics 105: 35-53. Lyttle, 1984, Genetics 106: 423-34. Mackay, Reynolds, and O'Donnell, 1985, Genetics 111: 885-904. genetics: Partially male fertile. Pu+ translocated to YS. Normal guanosine triphosphate cyclohydrolase (GTP CH) activity (Mackay et al., 1985). # T(Y;2)JL12 cytology: T(Y;2)YS;56F + In(2LR)21A;59D. new order: YL.YS|56F - 59D|21A; 60F - 59D|21A - 56F|YS. origin: /-ray-induced 2 rearrangement on T(Y;2)L141 = T(Y;2)56F. references: Lyttle, 1984, Genetics 106: 423-34. # T(Y;2)Kr: see T(Y;2)B80 # T(Y;2)KrAK1 cytology: T(Y;2)60F3-5. origin: X ray induced in If chromosome. references: Preiss, Rosenberg, Kienlin, Seifert, and Jackle, 1985, Nature 313: 27-32. genetics: Mutant for Kr. Incomplete revertant for If (pheno- type dependent on chromosomal background). molecular biology: Entire cloned Kr region (from -5 to +34) translocated onto Y; EcoRI site at origin of chromosomal walk of Preiss et al., 1985. # T(Y;2)MK2 cytology: T(Y;2)25E1-3. discoverer: Kotarski. # T(Y;2)odd2.31: see Tp(2;Y)odd2.31 # T(Y;2)odd4.13: see Tp(2;Y)odd4.13 # T(Y;2)odd4.25: see Tp(2;Y)odd4.25 # T(Y;2)prd5.12: see Tp(2;Y)prd5.12 # T(Y;2)SD: Translocation (Y;2) Segregation Distorter origin: X ray induced in SD-72 males carrying BSYy+ in translocations T(Y;2)SD-NE1, -NE2, and -NE3 and a normal Y in the other translocations. genetics: Associated with SD. K values tested. translocation cytology synonym ref ( __________________________________________________________________ T(Y;2)SD-L 58 T(Y;2)SD L2 2 T(Y;2)SD-L1 26B9-10 T(Y;2)SD72, T-1 1 T(Y;2)SD-L22 36B-C T(Y;2)SD72, T-22 1 T(Y;2)SD-L23 39B-C T(Y;2)SD72, T-23 1 T(Y;2)SD-L24 41 T(Y;2)SD72, T-24 1 T(Y;2)SD-L25 41 [within In(2LR)SD72 T(Y;2)SD72, T-25 1 = In(2LR)39-40;42A] T(Y;2)SD-L31 40-41 T(Y;2)SD72, T-31 1 T(Y;2)SD-L32 38A T(Y;2)SD72, T-32 1 T(Y;2)SD-L41 41B-C + T(Y;2)SD72, T-41 1 In(2LR)25A;41B-C T(Y;2)SD-NE1 31D T(Y;2)SD, EM106 1, 3 T(Y;2)SD-NE2 37B T(Y;2)SD, j-4 1, 3 T(Y;2)SD-NE3 | 42A T(Y;2)SD, EM135 1, 3 T(Y;2)SD-NE4 44D T(Y;2)SD, CB-1c 1, 3 T(Y;2)SD-YT1 42 T(Y;2)SD72-92 4 T(Y;2)SD-YT2 31 T(Y;2)SD72-132 4 T(Y;2)SD-YT3 37 T(Y;2)SD72-343 4 T(Y;2)SD-YT4 57 T(Y;2)SD72-398 4 ( 1 = Lyttle, 1977, Genetics 86: 413-45; 2 = Lyttle, 1979, Genetics 91: 339-57; 3 = Novitski and Ehrlich, 1970, DIS 45: 102; 4 = Yamazaki and Thompson, 1973, Jpn. J. Genet. 48: 217-29. | Suppresses SD strongly. # T(Y;2)TE34Ca: Translocation (Y;2) Transposing Element cytology: T(Y;2)35D5-7. Y arm not determined. origin: / ray induced as partial revertant of TE34Ca of Ising. discoverer: Gubb. synonym: T(Y;2)TE60V1. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. genetics: Variegates for the w+ of the transposing element. Male fertile. other information: Cytology not consistent with the insertion site of the transposing element. # T(Y;2)TE35A origin: / ray induced in TE35A. synonym: T(Y;2)TE146Z. T(Y;2)TE146Z translocation cytology discov ( __________________________________________________ T(Y;2)TE35A-18 35B1-2 1 T(Y;2)TE35A-51 35B1-2 3 T(Y;2)TE35A-102 35B T(Y;2)TE35A-201 35B 2 T(Y;2)TE35A-204 35B 2 T(Y;2)TE35A-206 35B [+ small Dp?] 2 T(Y;2)TE35A-211 35B + In(3R)CA52 2 T(Y;2)TE35A-213 35B 2 ( 1 = Roote; 2 = Samkange; 3 = Wilkins. # T(Y;2)TW20: Translocation (Y;2) Ted Wright cytology: T(Y;2)38A6-C1. origin: X ray induced. references: Wright, Hodgetts, and Sherald, 1976, Genetics 84: 267-85. genetics: Deficient for pr; carries Tft and l(2)74i. # T(Y;2)TW124 cytology: T(Y;2)45A2-E1. origin: X ray induced in cn bw. references: Wright, Hodgetts, and Sherald, 1976, Genetics 84: 267-85. genetics: Variegated for pr. # T(Y;2)w+Y Described as w+Y (see Y DERIVATIVES in SPECIAL CHROMOSOMES sec- tion). # T(Y;2;3)A147 cytology: T(Y;3)93F + T(2;3)60B;61A. origin: X ray induced. references: Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethmann, Hardy, Hessler, Miller, Nozawa, Parry, and Gould-Somero, 1972, Genetics 71: 157-84. # T(Y;2;3)b: see T(Y;2) - T(Y;2;3) # T(Y;2;3)b10-1 cytology: T(Y;2)YL;36D2-3 + T(2;3)36C10-D1;62A-B. new order: YLD|36D3 - 60; YS.YLP|36D2 - 36D1|62A - 61; 21 - 36C10|62B - 100. origin: X-ray-induced derivative of T(Y;2)b10; male fertile in combination with Df(1)bb158. references: Lyttle, 1984, Genetics 106: 423-34. genetics: 36C10-D1 breakpoint apparently inactivates rdo, since T(Y;2;3)b10-1/rdo flies exhibit a strong reduced-ocelli pheno- type. Males carrying the Y-chromosome element capped by 36D1-2 plus region 61 are viable and fertile; therefore Y-chromosome breakpoint distal to kl-5. Females carrying remaining two ele- ments of the translocation are marked with B and are sterile, presumably owing to heterozygous deficiency for region 61. This genotype, which is deficient also for 36D1-2 is deficient for Arr1, by in situ hybridization, and 1(2)36Db but not ninaD; whether kel is included not determined (Hardy). # T(Y;2;3)Coirv1: Translocation (Y;2;3) Coiled-revertant cytology: T(Y;2)22B8 + T(2;3)32F;89E-F + Tp(3;3)64C;71A;75C. new order: Y|21 - 22B8; 60 - 32F|89F - 100; 61 - 64C|71A - 75C|64C - 71A|75C - 89E|32F - 22B8|Y. origin: X ray induced. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. genetics: Revertant of Coi. #*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: YD|30A1 - 34C|78F - 100; YP|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. Indukt. Abstamm. Vererbungsl. 60: 235-86. genetics: Deficient for M(2)41A 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 YP2D element survives in hyperploids. # T(Y;2;3)F origin: X ray induced. discoverer: Dobzhansky, 1929. synonym: T(Y;2)F. references: 1930, Biol. Zentr. 50: 671-85. 1932, Z. Indukt. Abstamm. Vererbungsl. 60: 235-86. genetics: Break in 2R to right of sp. # T(Y;2;3)G20 cytology: T(Y;2;3)YS;31C-D;81F;82F. new order: YL.YS|81F - 82F|31C - 21; YS|31D - 60; 61 - 81F|82F - 100. origin: X ray induced. references: The Seattle-La Jolla Drosophila Laboratories, 1971, DIS 47, Suppl. Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethmann, Hardy, Hessler, Miller, Nozawa, Parry, and Gould-Somero, 1972, Genetics 71: 157-84. genetics: Male fertile over normal X. # T(Y;2;3)H: Translocation (Y;2;3) Hilliker origin: / ray induced. references: Hilliker and Trusis-Coulte, 1987, Genetics 117: 233-44. genetics: Viability and fertility of homozygotes not deter- mined. translocation ( cytology new order ______________________________________________________________ T(Y;2;3)H69 43B;98C YD|43B-21; YP|98C-100; 60-43B|98C-61. T(Y;2;3)H121 40-41;86B2-C1 not known T(Y;2;3)H159 37B;43D-E;64E;98C;het YL.YSP|?; YSD|98C-64E|37B-21; het|43D-37B|98C-100; het|43D-60; 61-64E|het. ( Synonym: T(Y;2;3)69 - T(Y;2;3)159. # T(Y;2;3)iab7MX1: Translocation (Y;2;3) infraabdominal 7 cytology: T(Y;2;3) (cytological breakpoints not given). origin: X ray induced. discoverer: Casanova. synonym: T(Y;2;3)Abd-BMX1; T(Y;2;3)iab6MX1. references: Sanchez-Herrero, Vernos, Marco, and Morata, 1985, Nature 313: 108-13. Karch, Weiffenbach, Peifer, Bender, Duncan, Celnicker, Crosby, and Lewis, 1985, Cell 43: 81-96. genetics: Viable over Df(3R)P9, showing strong transformation of the sixth and seventh abdominal segments to the fifth. molecular biology: DNA breakpoint at +126 to +129 kb, 0 being the 89E1-2 breakpoint of In(3R)Cbxrv1. #*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: YD|47A2 - 21; YD|91E4 - 99C|74B1 - 84E2|69C2 - 61; 60 - 47A3|YP|91E2 - 84E3|69C3 - 74A|99C - 100. origin: X ray induced. discoverer: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1932, Z. Indukt. Abstamm. Vererbungsl. 69: 235-86. # T(Y;2;3)SD-L12 cytology: T(Y;2)41A-B;62F5-6. origin: X ray induced in SD-72 males. synonym: T(Y;2;3)SD, T-12. references: Lyttle, 1977, Genetics 86: 413-45. genetics: K value 1.00. # T(Y;2;3)Ubx2P: Translocation (Y;2;3) Ultrabithorax cytology: T(Y;2;3)39;89E1-2;91F. origin: X ray induced. synonym: Ubx19849.2P. references: E.B. Lewis. genetics: Associated with Ubx. # T(Y;2;4)A96 cytology: T(Y;2;4)YL;59D;102. new order: YL|101; YS.YL|59D - 60; 21 - 59D|102. references: Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethmann, Hardy, Hessler, Miller, Nozawa, Parry, and Gould-Somero, 1972, Genetics 71: 157-84. genetics: Male fertile with normal X. # T(Y;2;4)ci12: Translocation (Y;2;4) cubitus interruptus cytology: T(2;4)46;102F + Tp(2;Y)54B;57B. Complex. new order: Y|(54B - 57B)|Y; 21 - 46|102F; 101 - 102F|46 - 54B|57B - 60. origin: X ray induced. synonym: R12(ci). references: Stern and Kodani, 1955, Genetics 40: 343-73. genetics: T(Y;2;4)ci12/ci males show less extreme L4 interrup- tions than ci/ci males. Usually no translocation females pro- duced because of Y linkage in T(Y;2;4)ci12. # T(Y;2;4)H161 cytology: T(Y;2;4)YS;35A-B;102. new order: YL.YS|102; YS|35B - 60; 21 - 35A|101. references: Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethmann, Hardy, Hessler, Miller, Nozawa, Parry, and Gould-Somero, 1972, Genetics: 71: 157- 84. # T(Y;2;4)J96 cytology: T(Y;2;4)h16;25A2-3;101-102 + Df(YL)BSXh;h8 (Y breaks from Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73). new order: BSXh|h8 - h16|25A3 - 60; Xhy+ - h16|102; 21 - 25A2|102 - 101. references: The Seattle-La Jolla Drosophila Laboratories, 1971, DIS 47: Suppl. Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethmann, Hardy, Hessler, Miller, Nozawa, Parry, and Gould-Somero, 1972, Genetics: 71: 157-84. Ashburner and Velissariou, 1980, DIS 55: 196. Velissariou and Ashburner, 1980, Chromosoma 77: 13-27. genetics: Male sterile. Shows variegation for dpov (Kotarski, Pickert, and MacIntyre, 1983, Genetics 105: 371-86. # T(Y;2;4)SD-L6 cytology: T(Y;2;4)40-41;101-102(?). (Presence of 4 based on its association with SD chromosome centromere). origin: X ray induced in SD-72 males. synonym: T(Y;2;4)SD, T-6. references: Lyttle, 1977, Genetics 86: 413-45. genetics: K value 1.00. # T(Y;3) origin: X ray induced using BSYy+. genetics: Male sterile in combination with Df(1)bb158. X/T(Y;3) translocation cytology (| ref / fertility | ____________________________________________________________________________ T(Y;3)A13 YL;68B 6, 7 + T(Y;3)A14 h3;63B 3, 6, 7 - T(Y;3)A23 h14;70B-C 3, 6, 7 - T(Y;3)A31 YS;70A-C 6, 7 - T(Y;3)A34 ` YS;76A-B;99A-B 4 + T(Y;3)A60 Xhy+;71C1-2 + 3, 6, 7 + In(3R)88A3-7;89A3-13 T(Y;3)A63 ` YL;68D;80-81 6, 7 - T(Y;3)A78 YL;87B5 1,3, 6, 7 - T(Y;3)A82 Xhy+;98F 3, 6, 7 + T(Y;3)A83 YL;61C 6, 7 + T(Y;3)A88 80-81 6, 7 + T(Y;3)A89 BSXhj;91B 3, 6, 7 (-) T(Y;3)A95 80-81 6, 7 + T(Y;3)A109 - YL;83E 6, 7 + T(Y;3)A112 h11;76E 3, 6, 7 + T(Y;3)A113 Xhy+;100A 3, 6, 7 + T(Y;3)A114 Xhy+;61A 3, 6, 7 + T(Y;3)A117 h24;96A 3, 6, 7 + T(Y;3)A121 h3;97D-E 3, 6, 7 - T(Y;3)A142 87D-88A 2 + T(Y;3)A148 80-81 6, 7 + T(Y;3)A150 YS;70D-E 6, 7 + T(Y;3)A154 BSXhj;82C 3, 6, 7 + T(Y;3)A155 YS;92A 6, 7 + T(Y;3)A158 YL;63A 6, 7 - T(Y;3)A173 h21;88B 3, 6, 7 - T(Y;3)A176 YL;76C 6, 7 - T(Y;3)A200 ` YL;64F;99D-F 6, 7 - T(Y;3)B12 80-81 6, 7 + T(Y;3)B20 ` 65F;80-81 6, 7 - T(Y;3)B21 YS;62C3-4 6, 7 - T(Y;3)B27 BSXh;94E 3, 6, 7 + T(Y;3)B49 YL;67D 6, 7 - T(Y;3)B64 ` 61A;72;85A 2 - T(Y;3)B68 ` h3;80-81;87A 3, 6, 7 - T(Y;3)B71 YS;61B-C 6, 7 + T(Y;3)B77 YL;61F 6, 7 - T(Y;3)B81 YL;99C-D + 6, 7 + In(3)80-81;87-88 T(Y;3)B82 80-81 6, 7 - T(Y;3)B93 h21;93F-94A 3, 6, 7 - T(Y;3)B96 YL;73A-B 6, 7 + T(Y;3)B99 YL;71F3-5 6, 7, 8 - T(Y;3)B108 Xhy+;77E-F 3, 6, 7 + T(Y;3)B115 h15;76D 3, 6, 7 + T(Y;3)B116 BSXhj;90E 3, 6, 7 + T(Y;3)B130 ` h1-2;61D-E;3R 3, 6, 7 - T(Y;3)B132 h23;76A 3, 6, 7 - T(Y;3)B141 ` YS;64E;68A 6, 7 - T(Y;3)B152 h3;98F 3, 6, 7 - T(Y;3)B154 ` 64C-D;80-81 6, 7 - T(Y;3)B155 YL;82C 6, 7 - T(Y;3)B158 BSXh;97B 3, 6, 7 + T(Y;3)B165 80-81 6, 7 - T(Y;3)B170 70D 6, 7 + T(Y;3)B172 YL;95A + 6, 7 + In(3R)93B-C;99A T(Y;3)B186 Xhy+;65E 3, 6, 7 (-) T(Y;3)B189 BSXhj;92D 3, 6, 7 + T(Y;3)B197 h3;96B1-10 3, 6, 7 - T(Y;3)B207 h25D;72D11-E1 3, 6, 7,8 + T(Y;3)B217 h3;96A1-5 3, 6, 7 - T(Y;3)B222 80-81 6, 7 - T(Y;3)B223 h13;72A-B 3, 6, 7 + T(Y;3)B225 YL;73D 6, 7 + T(Y;3)B226 BSXh;98B 3, 6, 7 + T(Y;3)B229 h13;64E + 3, 6, 7 + In(3R)94E-F;97C-D T(Y;3)B234 BSXhj;65B 3, 6, 7 + T(Y;3)B240 Xhy+;94B 3, 6, 7 + T(Y;3)D8 BSXhj;62A10-B1 6, 7 + T(Y;3)D85 - YS;84D7-9 6, 7 - T(Y;3)D100 h3;94A 3, 6, 7 - T(Y;3)D107 h7;82E 3, 6, 7 (kl3-- kl5-) T(Y;3)D210 71F 6, 7 - T(Y;3)D221 YS;96A 6, 7 - T(Y;3)D224 h21;64C-D 3, 6, 7 - T(Y;3)D226 BSXh;87E5-F2 1, 3, 6, 7 + T(Y;3)D227 5 + T(Y;3)D228 YL;74A3 1, 6, 7, 9 + T(Y;3)G7 YL;75C 6, 7 - T(Y;3)G8 YS;85F9-13 1, 6, 7 - T(Y;3)G11 h3;62E 3, 6, 7 - T(Y;3)G24 ` Xhy+;80-81;85D-E 3, 7 + T(Y;3)G42 h3;85E3 3, 6, 7 - T(Y;3)G43 Xhy+;63D2-E1 3, 6, 7 + T(Y;3)G45 h23;61E 3, 6, 7 - T(Y;3)G48 YS;88C 6, 7 + T(Y;3)G64 80-81 6, 7 - T(Y;3)G71 h21;67C 3, 6, 7 - T(Y;3)G72 80-81F 6, 7 - T(Y;3)G73 YL;96A1-5 6, 7 + T(Y;3)G75 YS;97B 6, 7 - T(Y;3)G101 80-81F 6, 7 (-) T(Y;3)G110 YL;91E-F 6, 7 - T(Y;3)G114 80-81 6, 7 (+) T(Y;3)G116 h3;99F (complex, 3, 6, 7 - (one break in 64C) T(Y;3)G122 h3;67C 3, 6, 7 - T(Y;3)G130 ` h23;61E;66B-C 3, 6, 7 + T(Y;3)G144 h3;83C 3, 6, 7 (+) T(Y;3)H61 80-81 6, 7 - T(Y;3)H133 80-81 6, 7 - T(Y;3)H135 h21;96C5-9 3, 6, 7 - T(Y;3)H138 ` YS;66B;66F 6, 7 + T(Y;3)H140 ` 66F;80-81 6, 7 - T(Y;3)H147 h3;77B 3, 6, 7 - T(Y;3)H153 80-81 6, 7 - T(Y;3)H156 YS;70C 6, 7 (+) T(Y;3)H159 80-81 6, 7 + T(Y;3)H163 YL;98B 6, 7 (+) T(Y;3)H167 66F-67A 2 T(Y;3)H172 BSXh;87F 3, 6, 7 + T(Y;3)H173 Xhy+;95E6-8 3, 6, 7 + T(Y;3)H175 ` 64E-F;81F 2 - T(Y;3)J1 ` 75C;81F 3,6 - T(Y;3)J17 Xhy+;82A 3, 6, 7 + T(Y;3)J23 h3;90D 3, 6, 7 - T(Y;3)J44 78C-D 3,6 - T(Y;3)J82 n 96A;97F 2 + T(Y;3)J94 h1-2;66B 3, 6, 7 - T(Y;3)J95 h21;78C 3, 6, 7 - T(Y;3)J100 h21;75C 3, 6, 7 - T(Y;3)J112 YS;71B3-8 6, 7,8 + T(Y;3)J116 BSXh;97E-F 3, 6, 7 + T(Y;3)J121 ` YL;61-65;95-96 6, 7 + T(Y;3)J128 h21;65F 3, 6, 7 - T(Y;3)J132 Xhy+;70C 3, 6, 7 + T(Y;3)J139 - YL;80 6, 7 + T(Y;3)J141 Xhy+;87A9-B3 1,3, 6, 7 + T(Y;3)J142 Xhy+;63E 3, 6, 7 + T(Y;3)J145 80-81 6, 7 + T(Y;3)J147 YS;76F-77A 6, 7 + T(Y;3)J150 YS;67D 6, 7 - T(Y;3)J151 YS;98E-F 6, 7 - T(Y;3)J154 YS;63A 6, 7 - T(Y;3)J162 ` h23;79E5-6;99E 3, 6, 7 + T(Y;3)L14 h3;76B5-10 3, 6, 7,9 - T(Y;3)L17 h16;86A6 + 1, 3, 6, 7 + In(3L)68B;73F T(Y;3)L18 Xhy+;64C13-15 3, 6, 7 - T(Y;3)L20 ` YS;64C-D;66E;79 2 - *T(Y;3)L60 YS;67D-E 6, 7 - T(Y;3)L61 80-81 6, 7 (+) T(Y;3)L65 80-81 6, 7 - T(Y;3)L68 80-81 6, 7 - T(Y;3)L111 h25D;92D-E 3, 6, 7 + T(Y;3)L113 h25D;71B-C 3, 6, 7 + T(Y;3)L125 Xhy+;94A 3, 6, 7 + T(Y;3)L129 h25D;100B-C 3, 6, 7 + T(Y;3)L130 ` 70D-E;87A 6, 7 - T(Y;3)L131 i Xhy+;75D1 1, 3, 6, 7,9 + T(Y;3)L132 YS;83C-D 6, 7 + T(Y;3)L136 BSXh;83E-F 3, 6, 7 + T(Y;3)L142 h3;89C 3, 6, 7 - T(Y;3)P31 80-81 6, 7 - T(Y;3)P40 5 + T(Y;3)P50 YL;65D 6 + T(Y;3)P60 YL;99F 6, 7 - *T(Y;3)R5 99A-B 7 - T(Y;3)R6 h3;92B 3, 6, 7 - T(Y;3)R7 BSXh;69F 3, 6, 7 + T(Y;3)R13 Xhy+;94E 6, 7 + T(Y;3)R24 ` 80-81 + Tp(3;3)91B-C;94C-E;98E 6, 7 - T(Y;3)R36 YL;86B 6, 7 + T(Y;3)R59 78F-79A 6, 7 - T(Y;3)R71 h1-2;97B 3, 6, 7 - T(Y;3)R78 h23;98E 3, 6, 7 - T(Y;3)R83 70B-C 5 T(Y;3)R86 h25D;66A 3, 6, 7 - T(Y;3)R87 YS;97A 6, 7 - T(Y;3)R91 BSXh;70C-D 3, 6, 7 + T(Y;3)R92 Xhy+;76C-D 5 T(Y;3)R98 65D-E 3, 6, 7 - T(Y;3)R100 80-81 6, 7 - T(Y;3)R106 BSXh;65D 3, 6, 7 + T(Y;3)R108 61B-C 5 - T(Y;3)R114 80-81 5 + T(Y;3)R117 h3;64E 3, 6, 7 - T(Y;3)R119 h23;66A 3, 6, 7 - T(Y;3)R122 Xhy+;69F 3, 6, 7 + T(Y;3)R128 97F 5 - T(Y;3)R130 h21;100A 3, 6, 7 - T(Y;3)R132 61F 6, 7 + T(Y;3)R133 BSXh;99E 3, 6, 7 + T(Y;3)R135 h25D;91B 3,6 + T(Y;3)R142 64D 5 - T(Y;3)R150 ` YL;64D;71B 6, 7 - T(Y;3)R153 YL;78A 6, 7 - T(Y;3)S50 BSXhj;61A 3, 6, 7 + ( Y breakpoints given in the terminology of Gatti and Pimpinelli, 1983, whenever available. | Parentheses used for data from Lindsley et al., 1972, that differ from data from The Seattle-La Jolla Drosophila Labora- tories, 1971, or Gatti and Pimpinelli, 1983. / 1 = Ashburner and Velissariou, 1980, DIS 55: 196; 2 = Baker, 1980, DIS 55: 197; 3 = Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73; 4 = Hazelrigg, Fornili, and Kaufman, 1982, Chromo- soma 83: 535-59; 5 = La Jolla Lab data (Rokop); 6 = Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethmann, Hardy, Hessler, Miller, Nozawa, and Gould-Somero, 1972, Genetics 71: 157-84; 7 = The Seattle-La Jolla Drosophila Laboratories, 1971, DIS 47, Suppl.; 8 = Velissariou and Ash- burner, 1981, Chromosoma 84: 173-85; 9 = Walker and Ashburner, 1981, Cell 26: 269-77. ` New order: T(Y;3)A34 = YL.YSP|99B - 100; YSD|76B - 99A|76A - 61. T(Y;3)A63 = YLD|80 - 100; YS.YLP|68D - 80|68C - 61. T(Y;3)A200 = YLD|99E - 64F|99D - 100; YS.YLP|64 - 61. T(Y;3)B20 = Y|65F - 80|65F - 61; Y|81 - 100. T(Y;3)B64 = YD|85A - 72|61A; YP|72 - 61A|85A - 100. T(Y;3)B68 = BSXh - h3|81 - 87A|80 - 61; Xhy+ - h3|87A - 100. T(Y;3)B130 = BSXh - h1|3RP - 61E|3RD - 100; Xhy+ - h2|61D - 61A. T(Y;3)B141 = BSXh - YSP|64E - 61; Xhy+ - YSD|68A - 64E|68A - 100. T(Y;3)B154 = Y|81 - 100; Y|64 - 80|64 - 61. T(Y;3)G24 = BSXh - Xhy+|85E - 100; Xhy+|81 - 85D|80 - 61. T(Y;3)G130 = BSXh - h23|61E - 66B|61E - 61A; Xhy+ - h23|66C - 100. T(Y;3)H138 = YL.YSP|66B - 61; YSD|66F - 66B|66F - 100. T(Y;3)H140 = Y|66F - 80|66F - 81; Y|81 - 100. T(Y;3)H175 = Y|64F - 81F|64E - 61; Y|81F - 100. T(Y;3)J1 = YP|81F - 100; YD|75C - 81F|75C - 61. T(Y;3)J121 = YLD|65 - 95|61; YS.YLP|96 - 100. T(Y;3)J162 = BSXh - h23|79D - 61; Xhy+ - h23|99E - 79D|99E - 100. T(Y;3)L20 = YL.YSP|64C - 61; YSD|66E - 64D|79 - 66E|79 - 100 (tentative). T(Y;3)L130 = YD|70E - 87A|70D - 61; YP|87A - 100. T(Y;3)R24 = Y|80 - 61; Y|81 - 91B|94E - 98E|94E - 91C|98E - 100. T(Y;3)R150 = YLD|71B - 64F|71B - 100; YS.YLP|64F - 61. - Immediately proximal [T(Y;3)A109] or distal [T(Y;3)D85] to the Antp complex (Kaufman, Lewis, and Wakimoto, 1980, Genetics 94: 115-33). Severe bb phenotype in combination with Df(1)bb158 (Golic). n The pieces 96A-97F and 97F-100 not visibly connected in chromo- center. - Breakpoints inferred from Bar-variegated phenotype (Craymer, 1984, DIS 60: 217). i Carries Cat+. # T(Y;3)12-4B cytology: T(Y;3)78F. origin: X ray induced on y+Y. references: Novitski and Ehrlich, 1970, DIS 45: 102. # T(Y;3)12-26M cytology: T(Y;3)83D. origin: X ray induced on y+Y. references: Novitski and Ehrlich, 1970, DIS 45: 102. # T(Y;3)15 origin: X ray induced. cytology: T(Y;3)87B5-7. references: Reuter, Dorn, Wustmann, Friede, and Rauh, 1986, Mol. Gen. Genet. 202: 481-87. Reuter, Gausz, Gyurkovics, Friede, Bang, Spierer, Hall, and Spierer, 1987, Mol. Gen. Genet. 210: 429-36. genetics: Associated with Su(var)3-6. #*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)67-325 cytology: T(Y;3)87B1-2. Complex rearrangement. origin: X ray induced. discoverer: Brosseau. references: Ellgaard and Brosseau, 1969, Genetics 62: 337-41. # T(Y;3)409 cytology: T(Y;3)87E1-2. origin: X ray induced. references: Reuter, Dorn, Wustmann, Friede, and Rauh, 1986, Mol. Gen. Genet. 202: 481-87. genetics: Associated with Su(var)3-7. # T(Y;3)Antprv: Translocation (Y;3) Antennapedia-revertant origin: X ray induced. genetics: Revertant of AntpNs [partial in T(Y;3)Antprv18]. homoz. translocation cytology synonym ref ( viable? ____________________________________________________________________ T(Y;3)Antprv3 84A4-B2 T(Y;3)AntpNs+R3 4, 5, 6 - T(Y;3)Antprv18 84A4-B2 T(Y;3)AntpNs+R18 4, 5 + T(Y;3)Antprv19 84B1-3 T(Y;3)AntpNs+R19 4, 5, 6 - T(Y;3)Antprv96 84B1-2;94C| T(Y;3)AntpNs+R96 1, 2, 3 - ( 1 = Denell, 1972, DIS 48: 45; 2 = Denell, 1972, Mutat. Res. 15: 221-23; 3 = Denell, 1973, Genetics 75: 279-97; 4 = Duncan and Kaufman, 1975, Genetics 80: 733-52; 5 = Kaufman, Lewis, and Wakimoto, 1980, Genetics 94: 115-33; 6 = Lewis, Kaufman, Denell, and Tallerico, 1980, Genetics 95: 367-81. | New order: YP|94C - 84B2|94C-100; YD|84B1 - 61. # T(Y;3)BSV14 cytology: T(Y;2)YL;80. discoverer: Craymer. # T(Y;3)bxdDB7 cytology: T(Y;3)89E. origin: X ray induced. discoverer: D. Baker. genetics: Mutant for bxd. # T(Y;3)CA12 cytology: T(Y;3)64C. origin: X ray induced simultaneously with Df(2L)el77 = Df(2L)35A1;35B3. synonym: T(Y;3)el77. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. # T(Y;3)CA16 cytology: T(Y;3)90B-C. references: Ashburner. genetics: Associated with Df(3L)DTS5-3 (Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91). # T(Y;3)CA49 cytology: T(Y;3)85E1-2. references: Ashburner. # T(Y;3)f4: Translocation (Y;3) free arms 4 cytology: T(Y;3)66C8-11;80. new order: 61 - 66C8|80 - 100; BSYL|80|66C11 - 82A|YSy+. origin: X ray induced in 3PYD elements of T(Y;3)J17 and T(Y;3)J139. references: Craymer, 1984, DIS 60: 217-18, 234-36. genetics: Phenotypically BS. #*T(Y;3)H58b: Translocation (Y;3) Hairless origin: / ray induced. discoverer: Ives, 58b25. references: 1959, DIS 33: 95. genetics: Mutant for H. #*T(Y;3)I cytology: T(Y;3)YS;63C;72E. new order: YL.YSP|63C - 72E|63C - 61; YSD|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 YP3LD ele- ment recoverable in hyperploid and duplicated for loci from ru through th. # T(Y;3)j3 cytology: T(Y;3)91A. origin: X ray induced in BSYy+. references: Novitski and Ehrlich, 1970, DIS 45: 102. # T(Y;3)j6 cytology: T(Y;3)91C. origin: X ray induced in BSYy+. references: Novitski and Ehrlich, 1970, DIS 45: 102. #*T(Y;3)K4: Translocation (Y;3) of Krivshenko cytology: T(Y;3)YS;81; inferred from metaphase cytology. Gan- glion metaphases show break in YS distal to bb and break in 3R near centromere. origin: X ray induced. discoverer: Krivshenko, 59b7. references: 1959, DIS 33: 96. genetics: Occasional homozygous males apparently sterile. # T(Y;3)Kpn+ cytology: Autosomal break in 3R tip. origin: X ray induced. references: Lifschytz and Falk, 1969, Genetics 62: 353-58. genetics: Recessive lethal. Revertant of awdK. # T(Y;3)MA9 cytology: T(Y;3)84B1-2. references: Lehmann and Nusslein-Volhard, 1987, Dev. Biol. 119: 402-17. # T(Y;3)P: Translocation (Y;3) Pasadena origin: X ray induced. translocation cytology discoverer ref ( _______________________________________________ T(Y;3)P3 61E-F Rosenthal 3 T(Y;3)P5 62C-D Rosenthal 3 T(Y;3)P6 | 62A-B Heinemann 3, 4, 5 T(Y;3)P26 87E-F E.B. Lewis 2 T(Y;3)P80 YL;88C-F E.B. Lewis 1, 6 T(Y;3)P102 87B1-2 E.B. Lewis 2 ( 1 = CP627; 2 = Ellgaard and Brosseau, 1969, Genetics 62: 337- 41; 3 = E.B. Lewis, 1969, DIS 44: 188; 4 = Ripoll and Garcia- Bellido, 1973, DIS 50: 177; 5 = Ripoll and Garcia-Bellido, 1978, Genetics 90: 93-104; 6 = Zuffardi, Tiepolo, Dolfini, Barigozzi, and Fraccaro, 1971, Chromosoma 34: 274-80. | Dp(Y;3)P6 carries all the fertility factors on the Y plus mwh+ and ve+ (Ripoll and Garcia-Bellido, 1973). Duplication product of T(Y;3)P5 but not T(Y;3)P3 also covers mwh (Lewis, 1969). # T(Y;3)pb2: Translocation (Y;3) proboscipedia cytology: T(Y;3)75C. origin: / ray induced simultaneously with, but independently of, pb2. references: Kaufman, 1978, Genetics 90: 579-96. # T(Y;3)PFA34 cytology: T(Y;3)YS;99B. origin: X ray induced. references: Hazelrigg, Fornili, and Kaufman, 1982, Chromosoma 87: 535-59. # T(Y;3)ru: Translocation (Y;3) roughoid origin: X ray induced. references: Hannah-Alava, 1968, Genetica 39: 94-132. genetics: Associated with ru. # T(Y;3)S: Translocation (Y;3) Schwartz origin: / ray induced. discoverer: Schwartz. references: Gatti and Pimpinelli, 1983, Chromosoma 83: 349-73. translocation cytology ( genetics ________________________________________ T(Y;3)S20 | y+Xh;{3R} kl-3- T(Y;3)S21 / h11;{3R} + kl-5- Df(YL)S21 T(Y;3)S22 h22;{chrom 3} ks-1 ( Break in chromosome 3 not determined. | Male sterile as homozygote and as heterozygote with T(Y;3)S21. / Male sterile as homozygote and as heterozygote with T(Y;3)S20. # T(Y;3)ScrE4: Translocation (Y;3) Sex combs reduced origin: Induced by ethyl methanesulfonate. discoverer: Kennison, 1984. genetics: Associated with Scr. # T(Y;3)sev: Translocation (Y;3) sepia-variegated cytology: T(Y;3)66D. origin: X ray induced. references: Jeffery, Stephans, and Giddings, 1974, Genetics 77: s32. genetics: Variegates for se. #*T(Y;3)sr100.23: 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)st100.126: 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;3)ST1 cytology: T(Y;3)YL;69F-70A2 + In(3L)62B;74A (Kennison). new order: YLP|69F - 62B|74A - 100. YS.YLP|70A2 - 74A|62B - 61. origin: / ray induced in a mwh iab9tuh3 stock. discoverer: Tiong. synonym: T(Y;3)12-10-1. genetics: Duplication segregant Dp(3;Y)ST1 includes brm+ th+ st+ tra+ KL+ KS+. # T(Y;3)Tabrv89: Translocation (Y;3) Tab-reverted cytology: T(Y;3)89E + In(3R)89E;90D. origin: X ray induced in In(3R)Tab. references: Celniker and Lewis, 1987, Genes and Development 1: 111-23. genetics: Revertant of the dominant Tab phenotype. When hemiz- ygous, shows stronger transformation of the eighth ventral setal band toward that of the seventh than does Tab/Df(3R)P9; also, A7 transformed toward A5 or A6, no posterior spiracles and no ninth ventral setal band. # T(Y;3)Ubx21R cytology: T(Y;3)89E. origin: X ray induced. synonym: Ubx19649.21R. references: E.B. Lewis. genetics: Associated with Ubx21R. # T(Y;3)Ubx1343 cytology: T(Y;3)89E. origin: X ray induced. synonym: Ubx31616.1343. references: E.B. Lewis. genetics: Associated with Ubx1343. # T(Y;3)vin101: Translocation (Y;3) vin cytology: T(Y;3)87F12-14. origin: / ray induced simultaneously with, but independently of, vin101. references: Akam, Roberts, Richards, and Ashburner, 1978, Cell 13: 215-25. genetics: Homozygous lethal but viable with all vin deficien- cies. # T(Y;3;4)fkh: Translocation (Y;3;4) fork head cytology: T(Y;3;4)98D2-3;99F;101. origin: X ray induced. references: Jurgens and Weigel, 1988, Roux's Arch. Dev. Biol. 197: 345-54. genetics: Weak fkh phenotype. # T(Y;4): see 4Y Described in section on Y derivatives. # T(Y;4)B15 cytology: T(Y;4)YL;102F. new order: BSYL|102F - 101A; 102F|YL.YSy+. origin: X ray induced using BSYy+. references: Hazelrigg, Fornili, and Kaufman, 1982, Chromosoma 83: 535-59. genetics: Male fertile as X/T(Y;4). # T(Y;4)ci1: Translocation (Y;4) cubitus interruptus origin: X ray induced. synonym: R1(ci). references: Stern and Kodani, 1955, Genetics 40: 343-73. other information: Breakpoints and position effect information not given.