TRANSLOCATIONS #*T(1;?)sc260-23: 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) Table I: Translocations with breaks in X euchromatin. cytology: X breaks based on salivary analysis (exceptions indicated in notes); Y breaks based on genetic data. origin: X ray induced. Translocations with unlettered desig- nations induced by Nicoletti; those with lettered designa- tions F, G and P-W (except P12) induced by Kennison; the remainder induced by Merriam and colleagues. genetics: Male viability and fertility indicated in table. break male T(1;Y)/0 translocation cytology in ref ( viable ? fertile ? ____________________________________________________________________ *T(1;Y)1 16F;YL y+Y 3,4 + T(1;Y)2 | 5E;11F;19F;YS y+Y 3,4 + T(1;Y)3 3E;YS y+Y 3,4 - T(1;Y)4 11A;YL y+Y 3,4 + T(1;Y)6 11D;YS y+Y 3,4 - *T(1;Y)8 4B;YL y+Y 3,4 + *T(1;Y)9 | 2C;19F;YS y+Y 3,4 + T(1;Y)10 3E;YL y+Y 3,4 + *T(1;Y)11 19F;YS y+Y 3,4 + *T(1;Y)13 7D;YL y+Y 3,4 - T(1;Y)14 19F;YS y+Y 3,4 + *T(1;Y)15 14F;YL y+Y 3,4 - T(1;Y)16 4C;YL y+Y 3,4 - *T(1;Y)18 19F;YS y+Y 3,4 + T(1;Y)19 17A;YL y+Y 3,4 + T(1;Y)20 11A;YL y+Y 3,4 + T(1;Y)21 1F;YL y+Y 3,4 + T(1;Y)22 19E;YS y+Y 3,4 + *T(1;Y)100 13F;YS BSY 3,4 - T(1;Y)101 19E;YS BSY 3,4 + T(1;Y)102 7D;YL BSY 3,4 + T(1;Y)103 19F;YS BSY 3,4 - T(1;Y)104 3D;YL BSY 3,4 + T(1;Y)105 19F;YS BSY 3,4 + T(1;Y)106 16A;YL BSY 3,4 + T(1;Y)107 / 3C8-12;YL BSY 3,4,7 + T(1;Y)108 5D;YL BSY 3,4 - T(1;Y)111 ` 3C;YL BSY 3,4 - T(1;Y)112 15A;YL BSY 3,4 - *T(1;Y)113 20A;YS BSY 3,4 + T(1;Y)114 3C;YL BSY 3,4 - T(1;Y)115 8F;YS BSY 3,4 - *T(1;Y)117 17A;YL BSY 3,4 + T(1;Y)118 16E;YL BSY 3,4 + T(1;Y)119 19F;YS BSY 3,4 + *T(1;Y)120 17E;YS BSY 3,4 - T(1;Y)122 20A;YS BSY 3,4 + *T(1;Y)123 19F;YS BSY 3,4 + T(1;Y)124 9F;YL BSY 3,4 + T(1;Y)125 15D;YL BSY 3,4 + T(1;Y)128 / 3C;YL BSY 3,4,7 - T(1;Y)129 11A;YL BSY 3,4 + T(1;Y)131 6E;YS BSY 3,4 + T(1;Y)132 19F;YS BSY 3,4 + T(1;Y)133 19E;YS BSY 3,4 + *T(1;Y)135 18C;YL BSY 3,4 + T(1;Y)137 19F;YS BSY 3,4 + *T(1;Y)139 20A;YS BSY 3,4 + T(1;Y)140 / 3C8-12;YL BSY 3,4,7 + T(1;Y)141 19E;YS BSY 3,4 + T(1;Y)142 13E;YL BSY 3,4 + T(1;Y)145 11B;YS BSY 3,4 + T(1;Y)147 8F;YS BSY 3,4 + *T(1;Y)148 2D;YL BSY 3,4 + T(1;Y)149 6E;YL BSY 3,4 + T(1;Y)150 3F;YS BSY 3,4 + T(1;Y)151 19F;YS BSY 3,4 + T(1;Y)152 13A;YL BSY 3,4 + T(1;Y)155 7B;YS BSY 3,4 - T(1;Y)156 7D;YL BSY 3,4 + *T(1;Y)157 14F;YL BSY 3,4 + *T(1;Y)158 11A;YL BSY 3,4 - T(1;Y)159 18A;YL BSY 3,4 + T(1;Y)164 / 3C;YL BSY 3,4,7 - *T(1;Y)169 11D;YS BSY 3,4 + T(1;Y)240 14A;YL BSY 3,4 + *T(1;Y)290 | 1A;20A;YS BSY 3,4 - T(1;Y)A1 12E;YL BSYy+ 2 + T(1;Y)A2 3F;YS BSYy+ 2 + + T(1;Y)A4 11A;YS BSYy+ 2 + + T(1;Y)A8 12F;YS BSYy+ 2 + + T(1;Y)B5 7C;YL BSYy+ 5 - T(1;Y)B6 14E-F;YS BSYy+ 5 _ *T(1;Y)B7 12B-C;Y BSYy+ 5 - T(1;Y)B8 16D;YL BSYy+ 5 - T(1;Y)B9 2A;YS BSYy+ 5 - T(1;Y)B10 16C3-5;YL BSYy+ 2,5,6 + + T(1;Y)B12 20;Y BSYy+ 5 + + *T(1;Y)B13 15D;YL BSYy+ 5 + + T(1;Y)B16 11B;YS BSYy+ 5 - T(1;Y)B17 7C;YS BSYy+ 2,5 + + T(1;Y)B18 16C;YL BSYy+ 2,5,6 + + T(1;Y)B24 12E;YL BSYy+ 2,5,6 + + T(1;Y)B25 15C;YS BSYy+ 2,5 + + T(1;Y)B26 9C;YS BSYy+ 2,5 + + T(1;Y)B28 13D;YS BSYy+ 2,5,6 + + T(1;Y)B29 4B;YL BSYy+ 2,5,6 + + T(1;Y)B31 - 20A1-3;YS BSYy+ 2,5 + + T(1;Y)B32 12D-E;YL BSYy+ 2,5 + + T(1;Y)B34 20A5-B1;YL BSYy+ 2,5 + + T(1;Y)B35 15A;YS BSYy+ 2,5,6 + + T(1;Y)B36 5C;YS BSYy+ 2,5,6 + + T(1;Y)B37 15C;YL BSYy+ 2,5 + + T(1;Y)B38 20F1;YS BSYy+ 2 + + T(1;Y)B39 11E-12A;YS BSYy+ 2,5,6 + + T(1;Y)B41 20B1-3;YL BSYy+ 2 + + T(1;Y)B43 20A1-3;YL BSYy+ 2,5 + + T(1;Y)B44 11A6-7;YL BSYy+ 2,5,6 + + T(1;Y)B45 11A6-7;YS BSYy+ 2,5 + + T(1;Y)B47 15C;YL BSYy+ 2,5 + + T(1;Y)B48 1A;3F;YS BSYy+ 5 + + T(1;Y)B49 11C-D;YL BSYy+ 2,5 + + T(1;Y)B50 - 18B9-10;YL BSYy+ 2,5 + + T(1;Y)B51 12F;YL BSYy+ 2,5 + + T(1;Y)B52 9A;YL BSYy+ 2,5 + + T(1;Y)B53 11A6-7;YS BSYy+ 2,5 + + T(1;Y)B54 12E;YS BSYy+ 2 + T(1;Y)B55 16F3-4;YS BSYy+ 2 + T(1;Y)B56 4F13-5A1;YL BSYy+ 2 + + T(1;Y)B57 9A1-2;YL BSYy+ 2 + T(1;Y)B59 11C1-2;YL BSYy+ 2 + T(1;Y)B60 9B;YS BSYy+ 2 + + T(1;Y)B61 - 20B1-3;YS BSYy+ 2 + + T(1;Y)B62 - 3D5-E1;YS BSYy+ 2 + + T(1;Y)B67 10E;YL BSYy+ 2 + T(1;Y)B75 16C-D;YS BSYy+ 2 + T(1;Y)B78 16C-D;YL BSYy+ 2 + + T(1;Y)B87 11A6-7;YL BSYy+ 2 + T(1;Y)B88 11E-F;YS BSYy+ 2 + + T(1;Y)B89 12B9-C1;YL BSYy+ 2 + T(1;Y)B90 15A;YS BSYy+ 2 + + T(1;Y)B91 20A5-B1;YS BSYy+ 2 + T(1;Y)B92 - 18A5-D1;YL BSYy+ 2 + T(1;Y)B93 - 19F5-20A1;YL BSYy+ 2 + T(1;Y)B94 20A5-B1;YL BSYy+ 2 + T(1;Y)B95 20A1-3;YL BSYy+ 2 + T(1;Y)B96 20A1-3;YS BSYy+ 2 + T(1;Y)B97 20B1-3;YL BSYy+ 2 + T(1;Y)B99 20A1-3;YL BSYy+ 2 + T(1;Y)B100 7F5-10;YL BSYy+ 2 + + T(1;Y)B101 - 19F1;YL BSYy+ 2 + T(1;Y)B102 16C-D;YL BSYy+ 2 + T(1;Y)B103 20B1-3;YS BSYy+ 2 + T(1;Y)B104 9A1-2;YL BSYy+ 2 + T(1;Y)B105 10A;YS BSYy+ 2 + T(1;Y)B106 1C;YL BSYy+ 2 + + T(1;Y)B107 - 18E1-19D1;YL BSYy+ 2 + T(1;Y)B108 20A1-3;YL BSYy+ 2 + T(1;Y)B109 20A1-3;YL BSYy+ 2 + T(1;Y)B110 4D;YL BSYy+ 2 + + T(1;Y)B111 11C;YL BSYy+ 2 + + T(1;Y)B112 11A6-7;YL BSYy+ 2 + + T(1;Y)B114 1F;YS BSYy+ 2 + + T(1;Y)B115 16C-D;YL BSYy+ 2 + T(1;Y)B116 14C;YS BSYy+ 2 + + T(1;Y)B117 13C-D;YL BSYy+ 2 + T(1;Y)B118 12F;YL BSYy+ 2 + T(1;Y)B119 - 5A6-9;YS BSYy+ 2 + + T(1;Y)B120 20A1-3;YL BSYy+ 2 + T(1;Y)B121 - 20B1-3;YL BSYy+ 2 + T(1;Y)B122 BSYy+ 1 + T(1;Y)B123 7B;YS BSYy+ 2,5 + T(1;Y)B124 12F;YL BSYy+ 2 + T(1;Y)B125 15A;YS BSYy+ 2 + + T(1;Y)B126 - 3C;YL BSYy+ 2 + + T(1;Y)B127 14A-B;YL BSYy+ 2 + + T(1;Y)B128 12F6-7;YS BSYy+ 2 + T(1;Y)B130 20A5-B1;YS BSYy+ 2 + T(1;Y)B131 2B;YL BSYy+ 2 + + T(1;Y)B132 17A9-12;YS BSYy+ 2 + T(1;Y)B133 12E;YL BSYy+ 2 + + T(1;Y)B134 20F1;YS BSYy+ 2 + T(1;Y)B135 9A;YL BSYy+ 2 + T(1;Y)B136 12C;YS BSYy+ 2 + + T(1;Y)B137 16F;YS BSYy+ 2 + + T(1;Y)B138 7F6-8;YL BSYy+ 2 + T(1;Y)B139 7F9-10;YL BSYy+ 2 + + T(1;Y)B140 16C-D;YL BSYy+ 2 + T(1;Y)B141 3F4-5;YL BSYy+ 2 + T(1;Y)B142 15C;YS BSYy+ 2 + + T(1;Y)B143 13D;YL BSYy+ 2 + T(1;Y)B144 16F;YS BSYy+ 2 + T(1;Y)B145 - 20A1-3;YL BSYy+ 2 + T(1;Y)B146 12E9;YL BSYy+ 2 + T(1;Y)B147 16F;YS BSYy+ 2 + T(1;Y)B148 10B;YS BSYy+ 2 + T(1;Y)B149 10A1-2;YL BSYy+ 2,8 + T(1;Y)B150 - 19D1-F1;YL BSYy+ 2 + T(1;Y)B151 14C;YS BSYy+ 2 + + T(1;Y)B152 9C;YL BSYy+ 2 + + T(1;Y)B153 - 2B8-10C;YS BSYy+ 2 _ T(1;Y)B154 19F5-20A1;YL BSYy+ 2 + T(1;Y)B155 20A1-3;YL BSYy+ 2 + T(1;Y)B156 16D;YL BSYy+ 2 + T(1;Y)B157 20A1-3;YL BSYy+ 2 + T(1;Y)B158 10A;YL BSYy+ 2 + T(1;Y)B159 16C-D;YS BSYy+ 2 + + T(1;Y)B160 BSYy+ 1 + T(1;Y)B161 - 18E1-4;YS BSYy+ 2 + T(1;Y)B162 14A-B;YS BSYy+ 2 + + T(1;Y)B163 4C-D;YS BSYy+ 2 + T(1;Y)B164 18A1-5;YS BSYy+ 2 + T(1;Y)B165 18A1-5;YS BSYy+ 2 + T(1;Y)B166 12A-B;YS BSYy+ 2 + T(1;Y)B167 9B;YS BSYy+ 2 + T(1;Y)B168 9B;YL BSYy+ 2 + + T(1;Y)B169 20A1-3;YL BSYy+ 2 + T(1;Y)B170 8A;YS BSYy+ 2 + T(1;Y)B171 BSYy+ 1 + T(1;Y)B172 - 18A1-5;YL BSYy+ 2 + T(1;Y)B173 - 19F2;YL BSYy+ 2 + T(1;Y)B188 12F6-7;Y BSYy+ 1 T(1;Y)C1 complex BSYy+ 5 - T(1;Y)C2 13E-F;YL BSYy+ 5 - T(1;Y)C4 4C;YL BSYy+ 5 _ T(1;Y)C5 complex BSYy+ 5 - T(1;Y)C7 17A5-6;Y BSYy+ 5 + - T(1;Y)C10 3E;7F;Y BSYy+ 5 + + T(1;Y)D1 8C;YS BSYy+ 2 + T(1;Y)D2 8C;YS BSYy+ 2 + T(1;Y)D7 - 3C;YS BSYy+ 2 _ + T(1;Y)D8 11A;YL BSYy+ 2 + T(1;Y)D9 11A6-7;YL BSYy+ 2 + T(1;Y)D10 5D5-6;YS BSYy+ 2 + T(1;Y)D12 7C;YL BSYy+ 2 + T(1;Y)D15 - 18E1-19D1;YL BSYy+ 2 + + T(1;Y)D16 ? BSYy+ 1 + T(1;Y)D17 4B;YS BSYy+ 2 + T(1;Y)F22 20A5-B1;YS BSYy+ 2 + + T(1;Y)G20 2B;YS BSYy+ 2 + + T(1;Y)J1 13A;YL BSYy+ 5 + + T(1;Y)J2a 9B;YS BSYy+ 2,5,6 + + T(1;Y)J6 20;Y BSYy+ 5 + + T(1;Y)J8 8C;YL BSYy+ 2,5,6 + + T(1;Y)J9 2C;YS BSYy+ 5 - T(1;Y)J10 17D-E;YS BSYy+ 2,5 + + (complex) T(1;Y)J11 20;Y BSYy+ 5 - T(1;Y)J14 1D;Y BSYy+ 5 - T(1;Y)J100 - 3C;YL BSYy+ 2 + + T(1;Y)J101 11E-F;YL BSYy+ 2 + T(1;Y)J102 5A1-3;YS BSYy+ 2 + + T(1;Y)J103 7B-C;YS BSYy+ 2 + + T(1;Y)J104 6E;YS BSYy+ 2 + + T(1;Y)J105 6E;YS BSYy+ 2 + + T(1;Y)J106 11E-F;YL BSYy+ 2 + T(1;Y)J107 20A1-3;YL BSYy+ 2 + + T(1;Y)J108 4D;YS BSYy+ 2 + + T(1;Y)J110 20A1-3;YS BSYy+ 2 + + T(1;Y)L1a 12E;YL BSYy+ 5 + + T(1;Y)L2a 9B;YS BSYy+ 2 + T(1;Y)L4 17B-C;YL BSYy+ 5,6 + + T(1;Y)L5 16F;YL BSYy+ 5 + + T(1;Y)M1 14A;Y BSYy+ 5 - T(1;Y)N3 20A5-B1;YL BSYy+ 2 + + T(1;Y)N5 - 19D1-F1;YS BSYy+ 2 + + T(1;Y)O15 2B;YS BSYy+ 2 + + T(1;Y)P3 20;Y BSYy+ 5 + + T(1;Y)P5 3C;Y BSYy+ 5 - T(1;Y)P6 18B;YL BSYy+ 5 _ T(1;Y)P7a 11C-D;Y BSYy+ 5 - T(1;Y)P8 18A;Y BSYy+ 5 + - T(1;Y)P11 18E1-19D1;YL BSYy+ 2 + + T(1;Y)P12 13F1-2;YS BSYy+ 2,5 + + T(1;Y)P21 15E;YL BSYy+ 5 + + T(1;Y)P22 3A;YS BSYy+ 5 - T(1;Y)Q6 20A1-3;YL BSYy+ 2 + + T(1;Y)R1 - 16F;YL BSYy+ 2 + - T(1;Y)R2 8D10-12;YL BSYy+ 2 + - T(1;Y)R4 15A9-11;YS BSYy+ 1 + - T(1;Y)R8 20A1-3;YL BSYy+ 2 + - T(1;Y)R20 16C-D;YL BSYy+ 2 + - T(1;Y)R30 - 3C;YL BSYy+ 2 + + T(1;Y)R34 - 18E1-4;YL BSYy+ 2 + - T(1;Y)R38 - 3C6;YL BSYy+ 2 + - T(1;Y)R44 7C;YL BSYy+ 2 + - T(1;Y)S10 20A1-3;YS BSYy+ 2 + + T(1;Y)S15 11B;YS BSYy+ 5 - T(1;Y)S19 14A3-5;YL BSYy+ 2 + - T(1;Y)S23 20;Y BSYy+ 5 + + T(1;Y)S27 7C;YL BSYy+ 2 + - T(1;Y)S29 13B4-6;YS BSYy+ 2 + - T(1;Y)S30 - 20A1-3;YS BSYy+ 2 + - T(1;Y)S31 - 18E1-19D1;YL BSYy+ 2 + - T(1;Y)S33 20;Y BSYy+ 5 + + T(1;Y)S34 BSYy+ 1 + - T(1;Y)S39 11C;YL BSYy+ 2 + - T(1;Y)T9 12F2-5;YL BSYy+ 2 + + T(1;Y)T12 [prox. to v];YL BSYy+ 1 + + T(1;Y)T16 14B2-5;YS BSYy+ 2 + + T(1;Y)V3 BSYy+ 1 + + T(1;Y)V7 16F4-8;YS BSYy+ 2 + + T(1;Y)V16 6E1-3;YL BSYy+ 2 + + T(1;Y)V29 16F4-8;YL BSYy+ 2 + + T(1;Y)V35 5B3-9;YL BSYy+ 2 + + T(1;Y)V46Df 20A1-3;YL BSYy+ 2 + + T(1;Y)V59 11F-12A;YL BSYy+ 2 + + T(1;Y)V61 11D2-5;YS BSYy+ 2 + + T(1;Y)V64 20A1-3;YL BSYy+ 2 + + T(1;Y)W14 - 5A9-13;YL BSYy+ 2 + + T(1;Y)W15 BSYy+ 1 + + T(1;Y)W16 - 19F1;YS BSYy+ 2 + + T(1;Y)W17 - 3C;YL BSYy+ 2 + + T(1;Y)W23 13E1-7;YL BSYy+ 2 + + T(1;Y)W31 7E2-3;YS BSYy+ 2 + + T(1;Y)W32 16F3-4;YS BSYy+ 2 + + ( 1 = Merriam; 2 = Merriam, Yamamoto, Stewart, Rahman, and Nicho- lau; 3 = Nicoletti and Lindsley, 1960, DIS 34: 95-97; 4 = Nicoletti and Lindsley, 1960, Genetics 45: 1705-22; 5 = Stewart and Merriam, 1973, DIS 50: 167-69; 6 = Stewart and Merriam, 1975, Genetics 79: 635-47; 7 = Young and Judd, 1978, Genetics 88: 723-42; 8 = Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Khudyakov, Patzevich, Semeshin, Bari- cheva, Aizenzon, Kramers, and Eeken, 1981, DIS 56: 192-96. | New order: T(1;Y)2 = 1 - 5E|YSP - YL; 20 - 19F|11F - 5E|19F - 11F|YSD. *T(1;Y)9 = 1A - 2C|YSP - YL; 20 - 19F|2C - 19F|YSD. *T(1;Y)290 = 1A|YSP - YL; 20F - 20A|1A - 20A|YSD. / 3C break between N and dm (Young and Judd, 1978). ` Variegates for w and N (Nicoletti and Lindsley, 1960). - Break locations inferred from crosses to deletions or lethals. Molecular biology: T(1;Y)B55 maps between +33.4 and +34.9 kb and T(1;Y)W32 maps between +95.2 and +98.7 kb (Kamb, Iverson, and Tanouye, 1987, Cell 50: 405-13). These and T(1;Y)V7 display leg shaking owing to their disruption of the Sh locus (Tanouye, Ferrus, and Fujita, 1981, Proc. Nat. Acad. Sci. USA 78: 6548-52). Table II: Translocations with breaks in X heterochromatin. cytology: Breakpoints on the cytogenetic map of the Y (Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73) and the X heterochromatin (Gatti and Pimpinelli, unpublished) inferred from the cytogenetic data of Kennison (1981, Genetics 98: 529-48) or, in a few cases, determined by Bonaccorsi. X breakpoints designated h26-h29 are distal to bb, those designated h29 are within bb and those designated h29-h33 are proximal to bb. Y breaks between BSXh and h17 are in YL; those between h18 and Xhy+ are in YS with bb occupying h20. origin: / ray induced using BSYy+. discoverer: Kennison. genetics: Male viable. Fertility of males indicated in table. male translocation cytology ( ref | fertility ______________________________________________________ T(1;Y)E1 h26-h29;h11 1,2 + T(1;Y)E5 h29;BS-h1 2 + T(1;Y)E12 h29;BS-h1 2 + T(1;Y)E15 h26-h29;h12-13 1,2 + T(1;Y)E17 h29-h33;BS-h1 2 + T(1;Y)F6 h29-h33;BS-h1 2 + T(1;Y)F12 h29;h15-h17 2 + T(1;Y)F14 h26-h29;h15-h17 2 + T(1;Y)F15 h29;h15-h17 2 + T(1;Y)G1 h29-h33;h18-h20 or 2 + h26-h29;h20-h21 T(1;Y)G7 h29-h33;h24-y+ 2 + T(1;Y)G8 h26-h29;h11-h12 1,2 + T(1;Y)G15 h26-h29;BS-h1 2 + T(1;Y)G22 h29;BS-h1 2 + T(1;Y)G24 h26-h29;BS-h1 2 + T(1;Y)G25 h26-h29;h13 1,2 + T(1;Y)G29 h29-h33;h18-h20 or 2 + h26-h29;h20-h21 T(1;Y)G30 h29;BS-h1 2 + T(1;Y)J2 h29-h33;h11-h13 2 + T(1;Y)K1 h29;BS-h1 2 + T(1;Y)L1 h29-h33;h20 or 2 + h29;h20-h25 T(1;Y)L2 h29-h33;h2-h3 2 kl-5 T(1;Y)N1 h29-h33;h18-h20 or 2 + h26-h29;h20-h21 T(1;Y)N10 h29-h33;h25-y+ 2 + T(1;Y)N12 h26-h29;h25-y+ 2 + T(1;Y)N13 h26-h29;h18-h20 2 + T(1;Y)N14 h26-h29;h18-h20 2 + T(1;Y)N16 h29;BS-h1 2 + T(1;Y)N18 h26-h29;h2-h3 2 kl-5 T(1;Y)N20 h29;h2-h3 2 kl-5 T(1;Y)N29 h29-h33;h11 1,2 + T(1;Y)N30 h29-h33;h25-y+ 2 + T(1;Y)P1 h29-h33;h25-y+ 2 + T(1;Y)P7 h29-h33;h11 1,2 + T(1;Y)P9 h29;BS-h1 2 + T(1;Y)R5 h29-h33;h10 2 kl-2 T(1;Y)R12 h26-h29;h25-y+ 2 + T(1;Y)R17 h29-h33;h4-h7 2 + T(1;Y)R19 h29-h33;h10 1,2 kl-2 T(1;Y)R21 h29-h33;h2-h3 2 kl-5 T(1;Y)R29 h29-h33;h2-h3 2 kl-5 T(1;Y)R36 h29;h2-h3 2 kl-5 T(1;Y)R39 h29-h33;h8-h9 2 kl-3 T(1;Y)R43 h29-h33;h15-h17 2 + T(1;Y)S1 h29-h33;h8-h9 2 kl-3 T(1;Y)S2 h26-h29;h8-h9 2 kl-3 T(1;Y)S7 h29-h33;h11-h13 2 + T(1;Y)S13 h26-h29;h11-h13 2 + T(1;Y)S20 h29-h33;h2-h3 2 kl-5 T(1;Y)S24 h29-h33;h8-h9 2 kl-3 T(1;Y)S25 h26-h29;h2-h3 2 kl-5 T(1;Y)S28 h29-h33;h11-h13 2 + T(1;Y)S32 h29-h33;h4-h7 2 + T(1;Y)S38 h29;h4-h7 2 + T(1;Y)T2 h29-h33;h2-h3 2 kl-5 T(1;Y)T4 h29;h2-h3 2 kl-5 T(1;Y)T6 h29-h33;h24-h25 2 ks-2 T(1;Y)T10 h26-h29;h21-h23 2 ks-1 T(1;Y)T11 h29-h33;h2-h3 2 kl-5 T(1;Y)T13 h29-h33;h8-h9 2 kl-3 T(1;Y)T17 h26-h29;h24-h25 2 ks-2 T(1;Y)T20 h26-h29;h25-y+ 2 + T(1;Y)T21 h26-h29;h21-h23 2 ks-1 T(1;Y)V4 h29-h33;h25-y+ 2 + T(1;Y)V8 h26-h29;h24 2 + T(1;Y)V13 h29-h33;BS-h1 2 + T(1;Y)V14 h26-h29;h18-h20 2 + T(1;Y)V23 h29-h33;h25-y+ 2 + T(1;Y)V24 h29-h33;h4-h7 2 + T(1;Y)V25 h29-h33;h25-y+ 2 + T(1;Y)V27 h26-h29;BS-h1 2 + T(1;Y)V30 h29-h33;h10 2 kl-2 T(1;Y)V31 h29-h33;h13 1,2 + T(1;Y)V32 h29-h33;h18-h20 or 2 + h26-h29;h20-h21 T(1;Y)V33 h29-h33;h21-h23 2 ks-1 T(1;Y)V36 h29-h33;h25-y+ 2 + T(1;Y)V43 h26-h29;h12-13 1,2 + T(1;Y)V47 h26-h29;h4-h7 2 + T(1;Y)V54 h29-h33;h21-h23 2 ks-1 T(1;Y)V57 h29-h33;h8-h9 2 kl-3 T(1;Y)V63 h26-h29;h11-h12 1,2 + T(1;Y)W1 h29-h33;h21-h23 2 ks-1 T(1;Y)W2 h26-h29;BS-h1 2 + T(1;Y)W3 h29-h33;h15-h17 2 + T(1;Y)W8 h29-h33;BS-h1 2 + T(1;Y)W9 h26-h29;h21-h23 2 - T(1;Y)W19 h29-h33;h20-h21 2 + T(1;Y)W28 h29-h33;h15-h17 2 + T(1;Y)W29 h29-h33;h18-h20 or 2 + h26-h29;h20-h21 T(1;Y)W30 h26-h29;BS-h1 2 + T(1;Y)W33 h29-h33;h15-h17 2 + T(1;Y)Z2 h26-h29;h11-h13 2 + T(1;Y)Z3 h26-h29;h21-h23 2 ks-1 T(1;Y)Z6 h29-h33;h14 1,2 kl-1 T(1;Y)Z13 h29-h33;h21-h23 1,2,3 ks-1 T(1;Y)Z14 h29-h33;h25-y+ 2 + ( The heterochromatic proximal part of the X has been divided by Gatti into 9 sections, h26-h34, distinguishable in neuroblast chromosomes by special staining techniques; the heterochromatic Y had previously been divided (Gatti and Pimpinelli, 1983) into 25 sections, h1-h25. The normal position of the X centromere is at h33-h34 and of the Y centromere at h17-h18. | 1 = Hardy, Lindsley, Livak, Lewis, Sivertsen, Joslyn, Edwards, and Bonaccorsi, 1984, Genetics 107: 591-610; 2 = Kennison, 1981, Genetics 98: 529-48; 3 = Kennison, 1983, Genetics 103: 219-34. # T(1;Y)1E: see Dp(1;Y)1E # T(1;Y)2E: see Dp(1;Y)2E # T(1;Y)B132 cytology: T(1;Y)17A9-12. origin: X ray induced. references: Baumann, Krah-Jentgens, Muller, Muller-Holtkamp, Seidel, Kecskemethy, Casal, Ferrus, and Pongs, 1987, EMBO J. 6: 3419-29. genetics: No Sh phenotype. # T(1;YS)118-2b: see X.YSYL118-2b # T(1;YS)A3: see X.YSA3 #*T(1;Y;2) origin: X ray induced. discoverer: Nicoletti. references: Nicoletti and Lindsley, 1960, Genetics 45: 1705- 22. 1960, DIS 34: 95-97. new translocation cytology order ( genetics _____________________________________________________________________ *T(1;Y;2)7 14F;YS + YL;36C 1 male lethal T(1;Y;2)17 7B;YL;39 2 male viable but sterile T(1;Y;2)109 | 3C;YL;40-41 male viable but sterile *T(1;Y;2)110 19D;55F + YS;45F 3 male viable but sterile *T(1;Y;2)130 | 11F;YL;40-41 male viable but sterile *T(1;Y;2)146 7D;YL + 20A;57F 4 male viable but sterile *T(1;Y;2)153 17A;YS;35D 5 male lethal *T(1;Y;2)160 | 17C;YS;40-41 male viable but sterile ( 1 = 1 - 14F|YSP - YLP|36C - 21; 20 - 14F|YSD; YLD|36C - 60. 2 = 1 - 7B|39 - 60; 20 - 7B|YLD; YS - YLP|39 - 21. 3 = 1 - 19D|55F - 45F|YSP - YL; 20 - 19D|55F - 60; YSD|45F - 21. 4 = 1 - 7D|YLP - YS; 20F - 20A|57F - 60; YLD|7D - 20A|57F - 21. 5 = 1 - 17A|35D - 60; 20 - 17A|YSD; YL - YSP|35D - 21. | Involvement of chromosome 2 inferred from genetic data; rear- rangement not cytologically observable in polytene chromosome preparations. # T(1;Y;2)C8 cytology: T(1;Y;2)12E;Y;26. origin: X ray induced in BSYy+. references: Stewart and Merriam, 1973, DIS 50: 167-69. genetics: Lethal. # T(1;Y;2;3)B46 cytology: T(1;Y;2;3)12E;Y;2R;3R. origin: X ray induced in BSYy+. references: Stewart and Merriam, 1973, DIS 50: 167-69. genetics: Viable, fertile. #*T(1;Y;3) origin: X ray induced. discoverer: Nicoletti. references: Nicoletti and Lindsley, 1960, Genetics 45: 1705- 22. 1960, DIS 34: 95-97. new translocation cytology order ( genetics ________________________________________________________________________________ *T(1;Y;3)5 11D;YL + 14F;72 1 male viable but sterile T(1;Y;3)121 6F;YS;86D 2 male lethal T(1;Y;3)127 19F;YS;85E 3 male viable but sterile *T(1;Y;3)134 12E;YS + 19E;62A 4 male viable but sterile *T(1;Y;3)136 7A;YL;70C 5 male viable but sterile *T(1;Y;3)138 11A;YL;84B 6 male viable but sterile T(1;Y;3)143 12A;YL + 3F;69C 7 male viable, sterile with free Y, lethal without T(1;Y;3)144 15E;YL;74D 8 male viable, sterile with free Y, lethal without T(1;Y;3)154 | 10B1-2;YS;97F11 9 male viable but sterile T(1;Y;3)161 17A;YL;94 10 male lethal ( 1 = 1 - 11D|YLP - YS; 20 - 14F|72 - 61; YLD|11D - 14F|72 - 100. 2 = 1 - 6F|YSP - YL; 20 - 6F|86D - 100; YSD|86D - 61. 3 = 1 - 19F|85E - 61; 20 - 19F|YSD; YL - YSP|85E - 100. 4 = 1 - 12E|YSP - YL; 20F - 19E|62A - 61; YSD|12E - 19E|62A - 100. 5 = 1 - 7A|70C - 100; 20 - 7A|YLD; YS - YLP|70C - 61. 6 = 1 - 11A|84B - 61; 20 - 11A|YLD; YS - YLP|84B - 100. 7 = 1 - 3F|69C - 100; 20 - 12A|YLD; YS - YLP|12A - 3F|69C - 61. 8 = 1 - 15E|74D - 100; 20 - 15E|YLD; YS - YLP|74 - 61. 9 = 1 - 10A|97A - 61; 20 - 10A|YSD; YL - YSP|97A - 100. 10 = 1 - 17A|94 - 61; 20 - 17A|YLD; YS - YLP|94 - 100. | Other references: Zhimulev, Belyaeva, Khudyakov, and Pokhol- kova, 1980, DIS 55: 211; Zhimulev, Pokholkova, Bgatov, Semeshin, and Belyaeva, 1981, Chromosoma 82: 25-40; Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 9-23. # T(1;Y;3)J4 cytology: T(1;Y;3)11A;Y;87. origin: X ray induced in BSYy+. references: Stewart and Merriam, 1973, DIS 50: 167-69. genetics: Lethal. # T(1;Y;3)V6 cytology: T(1;Y;3)1A;14B;18B1;YL;63A. origin: X ray induced in BSYy+. references: Merriam, Stewart, Nicholau, Yamamoto, and Rahman. genetics: Male viable. # T(1;Y;3)V17 cytology: T(1;Y;3)h29-h30;h11-12;75F-76A (Y breaks from Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73). new order: 1 - h29|h12 - Xhy+; h34 - h30|76A - 61; XhBS - h11|76A - 100. origin: / ray induced in BSYy+. references: Kennison, 1981, Genetics, 98: 529-48. Hardy, Lindsley, Livak, Lewis, Sivertsen, Joslyn, Edwards, and Bonaccorsi, 1984, Genetics 107: 591-610. genetics: Male viable and fertile. # T(1;Y;3)W27 cytology: T(1;Y;3)h29-h30;h9-h10;91A + In(Y)h10;h20 (Y breaks from Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73). new order: 1 - h29|h20 - h10|h20 - Xhy+; h34 - h30|91A - 100; XhBS - h9|91A - 61. origin: / ray induced in BSYy+. references: Kennison, 1981, Genetics, 98: 529-48. Hardy, Lindsley, Livak, Lewis, Sivertsen, Joslyn, Edwards, and Bonaccorsi, 1984, Genetics 107: 591-610. genetics: Male viable and fertile. Males carrying 3RPYD and XP3RD from T(1;Y;3)W27 and YPXD from T(1;Y)E15 are deficient for kl-2 and flanking sequences (Hardy et al., 1984). # T(1;Y;4)116 cytology: T(1;Y)14D;YS + T(1;4)9C;101. new order: 1 - 9C|101; 20 - 14D|YSD; YL - YSP|14D - 9C|102. origin: X ray induced in BSY. discoverer: Nicoletti. references: Nicoletti and Lindsley, 1960, Genetics 45: 1705- 22. 1960, DIS 34: 95-97. genetics: Male viable and sterile. # T(1;Y;4)BS: Translocation (1;Y;4) Bar of Stone cytology: A derivative of T(1;4)BS in which the X centromere has been replaced by a Y chromosome whose other arm (presum- ably YL) is derived from y+Y. references: Novitski and Peacock, 1970, DIS 45: 95-96. genetics: Males are viable with low fertility. # T(1;Y;A)V63 cytology: T(1;Y;A)h26-h29;h11-12;A (Y breaks from Gatti and Pimpinelli, 1983, Chromosoma 88: 349-73). new order: 1 - h26|h12 - Xhy+; h34 - h29|AD; XhBS - h11|AP. origin: / ray induced in BSYy+. references: Kennison, 1981, Genetics, 98: 529-48. Hardy, Lindsley, Livak, Lewis, Sivertsen, Joslyn, Edwards, and Bonaccorsi, 1984, Genetics 107: 591-610. genetics: Male viable and fertile. # T(1;2)1.10 cytology: T(1;2)4A3-4;24B. origin: X ray induced. discoverer: Nusslein-Volhard. synonym: T(1;2)odd1.10. references: Nusslein-Volhard, Kluding, and Jurgens, 1985, Cold Spring Harbor Symp. Quant. Biol. 50: 145-54. genetics: Male fertile. Second-chromosome breakpoint between odd and slp; neither gene mutant. The crossing scheme described should not have yielded X-autosome translocations. # T(1;2)2A4 cytology: T(1;2)11B;33E. origin: Induced by ethyleneimine. references: Lim and Snyder, 1968, Mutat. Res. 6: 129-37. #*T(1;2)7 origin: X ray induced. discoverer: Bonner, 1931. references: Dobzhansky, 1935, Z. Indukt. Abstamm. Vererbungsl. 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. XP2D 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: see Tp(1;2)26 # T(1;2)27A2 cytology: T(1;2)8E;57B. origin: Induced by ethyleneimine. references: Lim and Snyder, 1968, Mutat. Res. 6: 129-37. # T(1;2)63i: see Tp(1;2)v+63i # T(1;2)65b: see Tp(1;2)v65b #*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)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. Nat. 66: 193-206. Mackensen, 1935, J. Heredity 26: 163-74 (fig.). genetics: Mutant for N. # T(1;2)429.44 cytology: T(1;2)2B12-14;30B1-2. discoverer: Gelbart. # T(1;2)A18 cytology: T(1;2)2A4;60E8-9. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Mutant for br. #*T(1;2)A61b cytology: T(1;2)15F; breakpoint in chromosome 2 at unknown position in left arm, which also carries an inversion. Break- point 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)A64 cytology: T(1;2)2B7;42. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Mutant for br. # T(1;2)A1125: see Tp(1;2)rb+71g #*T(1;2)B48g: 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)sc4. discoverer: Yu, 48g. genetics: Position effect at B. Male sterile. # T(1;2)Bbd: Translocation (1;2) Bar-baroid cytology: T(1;2)16A1-2;48C2-3 + In(2R)41A;47A (Bridges in Mor- gan, Bridges, and Schultz, 1936, Year Book - Carnegie Inst. Washington 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)B27 origin: Induced in a Sh14 chromosome. references: Baumann, Krah-Jentgens, Muller, Muller-Holtkamp, Seidel, Kecskemethy, Casal, Ferrus, and Pongs, 1987, EMBO J. 6: 3419-29. genetics: Associated with modified Sh phenotype. molecular biology: Maps between 42 and 43 kb proximal to the start site of the Sh chromosomal walk. # T(1;2)Ba18: Translocation (1;2) Brista (J. Kennison) cytology: T(1;2)3C3-7;60D-E (J. Kennison). origin: Spontaneous. discoverer: Williams. synonym: Art; DllW; BaW. references: Cohen, Bronner, Kuttner, Jurgens, and Jackle, 1989, Nature 338: 432-34. molecular biology: 60D-E located on molecular map (Cohen et al., 1989). genetics: Associated with Ba18. 2PXD element is duplicated for the loci of y and w, deficient for M(2)60E and Kr and has the dominant Ba phenotype. # T(1;2)biD2: Translocation (1;2) bifid cytology: T(1;2)4C5-6;46B5-7. origin: X ray induced. references: Banga, Bloomquist, Brodberg, Pye, Larrivee, Mason, Boyd, and Pak, 1986, Chromosoma 93: 341-46. genetics: Associated with bi, Qd, and omb. 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 - 60F5. 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. Indukt. Abstamm. Vererbungsl. 64: 310-25. Bridges, 1937, Cytologia (Tokyo), Fujii Jub., Vol. 2: 745-55. Morgan, Bridges, and Schultz, 1938, Year Book - Carnegie Inst. Washington 37: 307. Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. genetics: Associated with Bld. Both aneuploid segregants sur- vive. The 2PXD element is duplicated for y, ac, sc, Hw, svr, su(s), l(1)1Ab, su(b), and M(1)1B and deficient for sp, bs, ba, Pin, and M(2)60E; heterozygote extreme Plexate and slight Minute with small dark body and slow development; viability low; male sterile; female slightly fertile. XP2D is recipro- cally duplicate deficient; heterozygous female Blond and extreme Minute [M(1)1B] with short, broad, occasionally downward-curved wings; ecloses 3-4 days late; male lethal, with embryos showing no organized ventral nerve cord structure but only some cell clusters in the brain lobes (Jim'nez and Campos-Ortega, 1979, Nature 282: 310-12). # T(1;2)C: Translocation (1;2) Crossover suppressor origin: X ray induced; selected on the basis of reduced recom- bination in one chromosome arm. discoverer: Roberts, 1964, 1965. references: 1970, Genetics 65: 429-48. new male male Xover translocation cytology order ( viable? fertile? reduced in _____________________________________________________________________________ T(1;2)C6 12E;40-41;60B 1 - 2R T(1;2)C20 12E;30B + - 2L T(1;2)C54 12E;32F - 2L T(1;2)C60 20;52B + + 2R T(1;2)C171 12A;40-41 + - X T(1;2)C176 20;40-41 + 2 - X In(1)8C-D;18D T(1;2)C179 9A;49A + 3 - X In(1)5C;20 T(1;2)C183 12E;40-41 + 4 - 2L In(2L)24C;30A T(1;2)C256 2A;40-41 + 5 - X In(1)7E;17A;18B T(1;2)C261 14C;40-41 + - X T(1;2)C262 11A;18A;40-41 6 - X T(1;2)C314 5D;40-41 + 9D;51D 7 + - X, 2R + 20;56F T(1;2)C324 | 15F;20;30A 8 - 2L T(1;2)C349 6C;47D + 9 - X In(1)2E;20 T(1;2)C357 20;56F + - 2R ( 1 = 1 - 12E|41 - 60B|40 - 21; 20 - 12E|60B - 60F. 2 = 1 - 8C|18D - 8D|18D - 20|41 - 60; 20|40 - 21 (tentative). 3 = 1 - 5C|20 - 9A|49A - 21; 20|5C - 9A|49A - 60. 4 = 1 - 12E|40 - 60; 20 - 12E|40 - 30A|24C - 30A|24C - 21 (tentative). 5 = 1 - 2A|41 - 60; 20 - 18B|17A - 18B|7E - 17A|7E - 2A|40 - 21. 6 = 1 - 11A|41 - 60; 20 - 18A|11A - 18A|40 - 21 (tentative). 7 = 1 - 5D|41 - 51D|9D - 5D|40 - 21; 20|56F - 51D|9D - 20|56F - 60 (tentative). 8 = 1 - 15F|20 - 15F|30A - 60; 20|30A - 21. 9 = 1 - 2E|20 - 6C|47D - 21; 20|2E - 6C|47D - 60. | Mutant or deficient for f. # T(1;2)C33 - T(1;2)C238 origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. mutant translocation cytology for ___________________________________________________ T(1;2)C33 2E3;41D kz T(1;2)C123 2B6;54A br T(1;2)C238 19E1-2;35A-B leg # T(1;2)clCA1: Translocation (1;2) clot cytology: T(1;2)1DE;25D7-E4. origin: X ray induced. discoverer: Velissariou. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. Velissariou and Ashburner, 1980, Chromosoma 77: 13-27. genetics: Associated with clCA1. # T(1;2)Clv3: Translocation (1;2) Cloven cytology: T(1;2)11A7-8;27E2-3 (Kirschbaum). origin: X ray induced in Binsc chromosome. references: Maroni, 1968, DIS 43: 60. genetics: Mutant for Clv. Male semi-lethal and sterile. #*T(1;2)ct7a1: 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; male lethal. #*T(1;2)ct268 origin: X ray induced. genetics: Male lethal. translocation cytology discoverer ( genotype _______________________________________________________________________ *T(1;2)ct268-17 7B2-5;41E2-4 (Hoover) 1 scp+ ct sn+ *T(1;2)ct268-24 7B2-5;41F6-42A1 2 scp+ ct sn+ *T(1;2)ct268-26 7B3-C1;36E 2 scp+ ct sn+ *T(1;2)ct268-32 | 1E-F;3D-E;7B2-5;46 1 fa+ dm+ scp+ (Hoover) ct sn+ *T(1;2)ct268-33 7B2-5;41E (Hoover) 1 ct sn+ *T(1;2)ct268-41 7B2-5;37C2-3 (Sutton) 1 cm+ ct sn+ ( 1 = Demerec; 2 = Hoover. | New order: 1A - 1E|3E - 7B2|46 - 21; 20 - 7B5|3D - 1F|46 - 60. # T(1;2)ctJ1 cytology: T(1;2)7B3-4;60E. origin: X ray induced. references: Lefevre and Johnson, 1973, Genetics 74: 633-45. genetics: Male lethal but somewhat viable with ct71g. # T(1;2)ctJ5 cytology: T(1;2)7B3-4;40. origin: X ray induced. references: Lefevre and Johnson, 1973, Genetics 74: 633-45. genetics: Male lethal but viable with ct71g. #*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)DEB: Translocation (1;2) diepoxybutane origin: Induced by diepoxybutane. references: Denell, Lim, and Auerbach, 1978, Mutat. Res. 49: 219-24. genetics: Male fertile. translocation cytology __________________________________ T(1;2)DEB1 5B;25E-F T(1;2)DEB2 5C;22E T(1;2)DEB3 20F;36D T(1;2)DEB4 20F;40-41 T(1;2)DEB5 1C;56C T(1;2)DEB6 20F;25A T(1;2)DEB7 20F;37D #*T(1;2)dorvar7: Translocation (1;2) deep orange-variegated cytology: T(1;2)2B8-9;40-41; + T(1;2)6F-7A;60C + In(2LR)35B;45A. new order: 1 - 2B8|40F - 35B|45A - 41A|2B9 - 6F |60C - 45A|35B - 21; 20F - 7A|60C - 60F. synonym: In(1)dorvar7(Belyaeva et al., 1982). references: Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kramers, and Zhimulev, 1982, D15 58: 184-90. Zhimulev, Belyaeva, Fomina, Protopopov, and Bolshakov, 1986, Chromosoma 94: 492-504. Demakova and Belyaeva, 1988, DIS 67: 19-20. Demakova, Belyaeva, and Zhimulev, 1988, DIS 67: 19-20. genetics: l(1)2Ad, l(1)2Ae, l(1)2Af, BRC, dor, and hfw translo- cated to 40F show position-effect variegation whose spread and type is affected by the source (maternal or paternal) of the rearrangement and the temperature (Demakova and Belyaeva, 1988). # T(1;2)dpp15: Translocation (1;2) decapentaplegic cytology: T(1;2)20;22F1-2. origin: X ray induced. discoverer: Spenser (Gelbart's lab). genetics: d-III dpp mutant. # T(1;2)dpp49 cytology: T(1;2)h33-34;22F. Cytology difficult; perhaps broken in XR. origin: / ray induced. discoverer: Irish. references: Gelbart. genetics: d-V dpp mutant. #*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)f257-22 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 BiBi. discoverer: Demerec, 36c. genetics: Mutant for f but B unaffected. Male lethal. # T(1;2)FN107: see Tp(1;2)sn+72d # T(1;2)GA origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. mutant translocation cytology for _________________________________ T(1;2)GA1 2E-F;41 T(1;2)GA26 2E3;23 kz T(1;2)GA113 2C;49A # T(1;2)GE204 cytology: T(1;2)3D3-4;60. origin: X ray induced. discoverer: Lefevre. genetics: Hemizygous lethal. # T(1;2)GE214 cytology: T(1;2)20A-B;27-28. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of l(1)20Ac. # T(1;2)GEM224 cytology: T(1;2)11A4;11C3;40-41. new order: 1 - 11A4|11C3 - 11A4|41 - 60; 21 - 40|11C3 - 20. discoverer: Lefevre. genetics: Mutant for fw (Kulkani and Hall, 1987, Genetics 115: 461-75). # T(1;2)GF326 cytology: T(1;2)1D4;36C. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of l(1)1Dc. # T(1;2)gl+: Translocation (1;2) giant larvae-wild type cytology: 21A1-C1 [location of l(2)gl] translocated to X tip. references: Cline, 1976, Genetics 83: s16. # T(1;2)HA37 cytology: T(1;2)3A4;32A1-2. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of l(1)3Ac. #*T(1;2)HC221 cytology: T(1;2)2B11;22B. origin: X ray induced. discoverer: Lefevre. genetics: Hemizygous lethal. Wild type over dor mutant; lethal over dor25 (Lefevre). # T(1;2)HC282 cytology: T(1;2)2C1-2;32B. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Not covered by Dp(1;3)wvco or y2Y67g (Lefevre). # T(1;2)HF326 cytology: T(1;2)3C7;27E. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. N allele. # T(1;2)HG370 cytology: T(1;2)3E3-4;A (complex). origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of slc. # T(1;2)Hwbap: Translocation (1;2) Hairy-wing-bristly abdominal pleura cytology: T(1;2)1B;21B (Cline, 1984). discoverer: Cline. references: Roseland and Schneiderman, 1979, Wilhelm Roux's Arch. Dev. Biol. 186: 235-65. Cline, 1984, Genetics 107: 231-77. 1988, Genetics 119: 829-62. genetics: Mutant for Hwbap. Deficient for al but not net (Cline). # T(1;2)K1: see Dp(1;2)K1 # T(1;2)KC16 cytology: T(1;2)2D5;52F. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Mutant for csw. # T(1;2)KW cytology: T(1;2)20;38C1 (Beermann). Heterochromatin translo- cated to Ddc region. origin: / ray induced. references: Bishop and Wright, 1987, Genetics 115: 477-91. # T(1;2)l-v: Translocation (1;2) lethal-variegated origin: X ray induced. discoverer: Lindsley, Edington, and Von Halle. references: 1960, Genetics 45: 1649-70. genetics: Selected as X chromosomes lethal or semilethal in XO males, but viable in XY males. Male sterile except for T(1;2)l-v135 which was not tested. translocation cytology ______________________________________ T(1;2)l-v25 ( 19-20;40-41 T(1;2)l-v75 19-20;41 T(1;2)l-v129 18B;41 T(1;2)l-v135 | 18-19;41 T(1;2)l-v150 16-17;40 T(1;2)l-v219 / 10A1-2;40 ( Position of breakpoint in chromosome 2 with respect to cen- tromere not determined. | Induced simultaneously with *T(2;3)135 = *T(2;3)37;85A. / Other references: Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Khudyakov, Patzevich, Semeshin, Baritcheva, Aizenzon, Kramers, and Eeken, 1981, DIS 56: 192-96; Zhimulev, Pokholkova, Bgatov, Semeshin, and Belyaeva, 1981, Chromosoma 82: 25-40. # T(1;2)L124 cytology: T(1;2)21C;XR. origin: / ray-induced detachment of C(1)RM, y2 su(wa) wa bb by the YP2D element of T(Y;2)L124. discoverer: Kennison. genetics: 21A-C appended to right arm of X chromosome. # 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)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. Indukt. Abstamm. Vererbungsl. 87: 708-21. genetics: Mutant for lz. # T(1;2)M: Translocation (1;2) Mglinetz references: Mglinetz, 1968, Genetika (Moscow) 4(8): 81-86. translocation cytology origin _______________________________________ T(1;2)M151 17F;44D / rays T(1;2)M154 11E;51B / rays T(1;2)M156 9A;47E / rays T(1;2)M158 10F;23C 32P feeding # T(1;2)N264: Translocation (1;2) Notch origin: X ray induced. discoverer: Demerec. translocation cytology ref ( variegates for __________________________________________________________________ *T(1;2)N264-9 {3C;41} 1 rst N dm w | a(2) M(2)41a T(1;2)N264-10 / 1 rst N dm *T(1;2)N264-23 3C8-9;41A 2 rst fa (Demerec and Hoover) *T(1;2)N264-24 3C8-9;40F (Demerec) 2 w rst fa *T(1;2)N264-53 ` 3C6-7;34C7-D1 2 *T(1;2)N264-59 3C8-9;40F (Hoover) 2 w rst spl *T(1;2)N264-62 3C7-8;41A-B (Sutton) 2 w rst fa *T(1;2)N264-66 3C6-7;41 + 7C9-D1;53F 1 w rst fa dm ec (Hoover) *T(1;2)N264-69 - 3C7-8;44C4-5 (Demerec) 2 *T(1;2)N264-82 3C3-4;41A + 20A;57 1 w rst fa dm (Demerec) ( 1 = CP627; 2 = Demerec, 1941, Proc. Int. Congr. Genet. 7th, pp. 99-103. | w variegation occurs at low temperatures. / XY male lethal; XYY male survives. ` Carries mutant alleles of rst, fa, dm. - Carries mutant allele of N. # T(1;2)NSt: see Tp(1;2)w-ec #*T(1;2)N4 cytology: T(1;2)3A5;55A. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of l(1)3Ac. # T(1;2)OR: Translocation (1;2) from Oak Ridge origin: X ray induced; recovered by virtue of pseudolinkage in daughters of irradiated wild-type males. discoverer: Warters, 1959, 1961. translocation cytology genetics ______________________________________________________________________________ T(1;2)OR6 ( 2A;60D male viable, fertile; homozygous female viable T(1;2)OR7 3A;41E XY male lethal; with BSw+Y, male viable but sterile T(1;2)OR8 | 20;40-41 male viable, fertile; homozygous female viable T(1;2)OR11 14F;41 variegated for a lethal; XY male viable but sterile T(1;2)OR14 18D;46B male quite inviable; rare survivor has unexpanded wings and crossed scutellars. T(1;2)OR15 11B;60E male viable but sterile T(1;2)OR17 3C;37C male viable but sterile with Y or BSw+Y T(1;2)OR18 / 20B;30E male viable but sterile T(1;2)OR20 16C;43B male lethal (lethal appeared later) T(1;2)OR21 19E;32D male lethal T(1;2)OR22 8D;22B male lethal T(1;2)OR23 6B;40 male viable but sterile T(1;2)OR25 1B;38E male viable but sterile T(1;2)OR26 15A;41 male viable but sterile; XO male has melanotic, distended wings T(1;2)OR27 16D;34B male viable but sterile T(1;2)OR28 3B;39E male viable but sterile with Y or BSw+Y T(1;2)OR29 8D;40 male viable but sterile T(1;2)OR30 | 20;40-41 male viable but sterile T(1;2)OR32 ` 20;54A male viable but sterile T(1;2)OR33 17;47A male viable but sterile T(1;2)OR36 | 20;40-41 male viable but sterile T(1;2)OR37 10A;50C male viable but sterile T(1;2)OR38 20B;50A male lethal T(1;2)OR39 1D;46E male viable but sterile T(1;2)OR41 12D;25E male lethal T(1;2)OR42 12F;58F male lethal T(1;2)OR43 15E;40D male viable but sterile, with small rough eyes (un?) T(1;2)OR44 16F;28F male viable but sterile T(1;2)OR45 | 7D;40-41 male viable but sterile T(1;2)OR47 19E;53B male viable but sterile T(1;2)OR48 17A;31F male viable but sterile T(1;2)OR49 | 20;40-41 male viable but sterile T(1;2)OR50 19C;33F male viable, fertile; homozygous female weakly viable T(1;2)OR51 8D;41F male lethal (lethal originated after translocation) T(1;2)OR52 4F;41A male viable but sterile T(1;2)OR54 19E;32E male viable but sterile with slightly curled wings T(1;2)OR55 20A;44D male viable but sterile T(1;2)OR56 18F;47D male lethal T(1;2)OR58 |/- 11B;40-41 male lethal +19C;30B T(1;2)OR59 ` 19E;57B male lethal T(1;2)OR60 10A;52D male viable but sterile T(1;2)OR61 18D;31F male viable but sterile T(1;2)OR62 |- 8F;17F;40-41 male lethal T(1;2)OR64 11A;53F male lethal T(1;2)OR65 7A;40 male lethal T(1;2)OR66 8B;23C male viable, fertile T(1;2)OR67 - 12B;41 + 20A;45B male viable, fertile T(1;2)OR68 - 16E;41 + male viable but sterile Tp(2;2)25E;33A;40 T(1;2)OR69 3C;41C variegated for lethal; male sterile with Y or BSw+Y T(1;2)OR72 - 19E;29F + male viable but sterile In(2LR)24F;54B T(1;2)OR73 ` 19E;57E male viable but sterile T(1;2)OR74 ` 19E;56C male viable but sterile T(1;2)OR75 12E;32B male lethal T(1;2)OR78 / 19E;30B male viable but sterile T(1;2)OR82 13D;30B male viable but sterile T(1;2)OR83 12A;22B male lethal T(1;2)OR84 3C;38E male viable but sterile with Y or BSw+Y T(1;2)OR85 10;38 male viable but sterile T(1;2)OR86 11A;32B male viable but sterile ( 2PXD element can replace one chromosome 2, producing a defi- ciency for tip of 2R; resulting progeny Minute since M(2)60E in the deficiency. | Positions of second-chromosome breakpoint(s) with respect to centromere not determined. / Male hyperploid for XP2LD element survives, has outstretched wings. ` Male hyperploid for XP2RD element survives. - T(1;2)OR58 = 1 - 11B|40 - 30B|19C - 11B|41 - 60; 20 - 19C|30B - 21. T(1;2)OR62 = 1 - 8F|40 - 60; 20 - 17F|8F - 17F|40 - 21 (tentative). T(1;2)OR67 = 1 - 12B|41 - 45B|20A; 21 - 41|12B - 20A|45B - 60. T(1;2)OR68 = 1 - 16E|41 - 40|(25E - 33A)|40 - 33A|25E - 21; 20 - 16E|41 - 60 (tentative). T(1;2)OR72 = 1 - 19E|29F - 54B|24F - 21; 20 - 19E|29F - 24F|54B - 60. Male hyperploid for XP2lM2RD element survives. # T(1;2)paralk1: Translocation (1;2) paralytic cytology: T(1;2)14C7-D1;41A. references: J.C. Hall. genetics: Mutant for para. # T(1;2)pn20: Translocation (1;2) prune cytology: T(1;2)2E1-2;40C1-2. references: Slobodyanyuk and Serov, 1983, Mol. Gen. Genet. 191: 372-77. genetics: Mutant for pn. # T(1;2)pn40 cytology: T(1;2)2E1-2;41A. origin: X ray induced. references: Ilyina, Sorokin, Belyaeva, and Zhimulev, 1980, DIS 55: 205. Slobodyanyuk and Serov, 1983, Mol. Gen. Genet. 191: 372-77. genetics: Mutant for pn. Homozygous lethal. # T(1;2)RC45 cytology: T(1;2)3A4;3C1-2;59D. new order: 1 - 3A4|3C1 - 3A4|59D - 21; 20 - 3C2|59D - 60. origin: X ray induced. discoverer: Lefevre. references: Young and Judd, 1978, Genetics 88: 723-42. genetics: 3C break between w and rst; not lethal. Allele of l(1)3Ac. # T(1;2)RC66 cytology: T(1;2)1E4;58E. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. #*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)RF19 cytology: T(1;2)20;2L + Df(1)7A4;7B2-3 + In(1)6A1;19E8. origin: X ray induced. discoverer: Lefevre. references: Johnson and Judd, 1979, Genetics 92: 485-502. genetics: Associated with Df(1)RF19 and In(1)RF19. # T(1;2)RF45 cytology: T(1;2)19E;20E-F;52A. new order: 1 - 19E|52A - 21; 20F|19E - 20E|52A - 60. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of run (Lefevre). # T(1;2)S25: Translocation (1;2) of Segal cytology: T(1;2)20?;50F. origin: / ray induced with T(2;3)shvS25. references: Segal and Gelbart, 1985, Genetics 109: 119-43. # T(1;2)S76 cytology: T(1;2)3A4;42A. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of l(1)3Ac. #*T(1;2)sc115: Translocation (1;2) scute cytology: T(1;2)1A6-B1;25F; inferred from fig. 3 of Goldat. origin: X ray induced derivative of sc6. discoverer: Goldat. references: 1936, Biol. Zh. (Moscow) 5: 803-12. genetics: Mutant for sc. #*T(1;2)sc260-17 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)scS2: Translocation (1;2) scute of Sinitskaya cytology: T(1;2)1B4-7;60C-E. discoverer: Sinitskaya, 1934. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. genetics: Mutant for sc. X chromosome broken to the right of l(1)sc in same place as right breakpoint of Tp(1;2)sc19 and 2R broken between sp and M(2)60E (Muller). Aneuploid segregants 2PXD and XP2RD should survive. molecular biology: X breakpoint between left breakpoints of In(1)sc9 and In(1)sc7 (Campuzano, Carramolino, Cabrera, Ruiz- Gomez, Villares, Bononat and Modell, 1985, Cell 49: 327-38). # T(1;2)shvS26: Translocation (1;2) short vein cytology: T(1;2)1D;22F1-2. origin: / ray induced. references: Segal and Gelbart, 1985, Genetics 109: 119-43. genetics: Associated with shv. Lethal with shv and l(2)DPP alleles. # T(1;2)SP1: Translocation (1;2) from Sao Paulo origin: / ray induced. Selected as X-linked male-sterile muta- tions in a y w X chromosome. discoverer: Lindsley and Musatti, 1961. translocation cytology genetics __________________________________________________________ T(1;2)SP1 8B;41 variegated for a lethal T(1;2)SP4 20;40-41 T(1;2)SP10 ( 10D4-6;50D5-7 T(1;2)SP16 20;40-41 T(1;2)SP18 1A;56A male fertile T(1;2)SP19 20;40-41 homozygous female fertile T(1;2)SP20 20;40-41 T(1;2)SP31 | 20;56B *T(1;2)SP33 14;41 T(1;2)SP36 20;40-41 T(1;2)SP42 20;40-41 T(1;2)SP43 16A;60C T(1;2)SP48 15F;35A T(1;2)SP49 12;40-41 T(1;2)SP50 / 20;29-30 T(1;2)SP51 20;40-41 T(1;2)SP52 12E;57F T(1;2)SP55 ` 1A;41 + 4B;30B male lethal + In(1)12D;14B T(1;2)SP58 10A;34A T(1;2)SP60 17E;35A T(1;2)SP61 18F;47D T(1;2)SP64 3C;28C male sterile with Y or BSw+Y T(1;2)SP67 20;40-41 T(1;2)SP69 7C;41 T(1;2)SP71 20;40-41 *T(1;2)SP75 8C;35D T(1;2)SP77 9A;41 T(1;2)SP81 / 20;24F-25A T(1;2)SP84 4C;42C T(1;2)SP87 9A4-B1;58A3-4 T(1;2)SP88 / 20;32F-33A *T(1;2)SP89 4E;35A mutant for rg? T(1;2)SP93 / 18C-D;22A-B T(1;2)SP94 14B-C;23F T(1;2)SP96 20;40-41 *T(1;2)SP97 9E-F;35A-B T(1;2)SP102 16A;41 *T(1;2)SP106 6B;40 T(1;2)SP110 13A;57E T(1;2)SP111 20;41-41 ( See Lefevre, 1970, DIS 45: 39. | Male hyperploid for XP2RD element survives. / Male hyperploid for XP2LD element survives. ` New order: 1A|41 - 30B|4B -1A|41 - 60; 20 - 14B|12D -14B|12D - 4B|30B - 21. #*T(1;2)Sy: Translocation (1;2) Stubby origin: Spontaneous. discoverer: Ives, 34j31. genetics: Associated with Sy. Male sterile. Probably recipro- cal translocation with breaks near the base of X and 2L. # T(1;2)TE35A-217: Translocation (1;2) Transposing Element cytology: T(1;2)20;35A-B. origin: / ray induced in TE35A. discoverer: Samkange (Ashburner's lab). synonym: T(1;2)TE146-217. #*T(1;2)v267-4 cytology: T(1;2)11A7-8;36 (Sutton). origin: X ray induced. discoverer: Hoover, 35i. genetics: Mutant for v (breakpoint not at v locus). Semi- lethal. ras, dwx, sbr, m, dy, and fw not affected. # T(1;2)V: Translocation (1;2) Valencia origin: X ray induced. references: Valencia, 1970, DIS 45: 37. translocation cytology genetics __________________________________________________ T(1;2)V9-2 6A2-3;38F male sterile T(1;2)V11-2 20;40-41 male fertile, homozygous viable T(1;2)V12-1 11E-F;25C-D male sterile T(1;2)V12-2 12C9;40-41A male sterile T(1;2)V101 20A(C-D?);60F5 male sterile T(1;2)V153 20A3-4;56F5 male sterile T(1;2)V154 12A3;40-41 lethal T(1;2)V161 8B4;40 lethal # T(1;2)VE614 cytology: T(1;2)7B1-2;2L. origin: Induced by ethyl methanesulfonate. references: Lefevre and Leeds, 1983, Genetics 104: s45-46. genetics: Shows strong kf2 phenotype but has no ct effect. # T(1;2)VE715 cytology: T(1;2)19E;27A. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. unc allele. # T(1;2)VE901 cytology: T(1;2)2B;25E-F. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Mutant for br. #*T(1;2)w13G2: Translocation (1;2) white cytology: T(1;2)3C3-5;41;56F; also inversion in 2R. new order: 1 - 3C3|41 - 56F|41 - 21; 20 - 3C5|56F - 60. Probable. origin: X ray induced. discoverer: Gans. genetics: Variegated for w. # T(1;2)w64d: see Tp(1;2)w-ec # T(1;2)w70k18.1 cytology: T(1;2)3C1;12B2-9;39E2. new order: 1 - 3C1|39E3 - 60; 21 - 39E2|12B2 - 3C2|12B9 - 20. origin: X ray induced in In(1)z64b9. references: Sorsa, Green, and Beermann, 1973, Nature (London) New Biology 245: 34-37. genetics: Male viable with white eyes. # T(1;2)w+51b7: see T(1;2)51b #*T(1;2)wm53e: Translocation (1;2) white-mottled 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(X.2)InX and 3. references: 1963, DIS 38: 29. genetics: Variegated for w. #*T(1;2)wm258-34 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)wm258-36 cytology: T(1;2)3C6-7;41A-B + T(1;2)4C2-3;41F5-6. new order: 1 - 3C6|(41B - 41F5)|4C3 - 20; 21 - 41A|(3C7 - 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)wm258-37 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)wm258-39 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)wm258-40 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)wmD1: 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)wvD4: 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)64d: see Tp(1;2)w-ec # T(1;2)w-ec: see Tp(1;2)w-ec # T(1;2)X9ts cytology: T(1;2)2D1-2;56A1-2. origin: / ray induced. references: Kaufman and Suzuki, 1974, Can. J. Genet. Cytol. 16: 579-92. genetics: Male fertile. Associated with temperature-sensitive lethal in males. X/X females and X/w+Y males are viable and normal at 22 and 29; X/Y males at 29 are lethal or show escaper phenotype of net-like wing veins, etched abdominal tergites, and sexcombs on meso- and metathoracic legs. #*T(1;2)y260-13: 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)yA76b37 cytology: T(1;2)1B1-2;60F. origin: / ray induced. references: Alexandrov, Ankina, and Alexandrova, 1985, DIS 61: 212-13. genetics: Mutant for a yc4-like allele. # T(1;2)yA79d cytology: T(1;2)1A6-B2;23E5. origin: Neutron induced. references: Alexandrov, Ankina, and Alexandrova, 1985, DIS 61: 212-13. genetics: Mutant for y. # T(1;2)yR7 cytology: T(1;2)1A6-B1;49F. origin: X ray induced. references: Roberts, 1974, Mutat. Res. 22: 139-44. genetics: Body color yellow. Male viable but sterile. #*T(1;2)yv1: 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)z+: Translocation (1;2) zeste-wild type origin: X-ray-induced rearrangements in z-bearing X chromosomes that interfere with the z-w interaction. genetics: z+ phenotype. translocation cytology ref ( ________________________________________________ T(1;2)z+3a 3C2-3;chromosome 2 2 T(1;2)z+4E6 3C3-5;40A 1 T(1;2)z+6E8 3E2-6;25E + X distal;80-81 T(1;2)z+14E9 3B2-C1;19B2-C1;24D4-E1 1 T(1;2)z+20 3C1-2;43E 2 T(1;2)z+23 3C1;3D;40 2 T(1;2)z+29 3C1;37C + Dp(1;2)2E1;3B4-C1;22D2-3 T(1;2)z+35 3C6-7;23A4-B1 2 T(1;2)z+36 3C3;54F-55A 2 T(1;2)z+43 3C1-2;37F 2 T(1;2)z+49 3C;55D-E 2 T(1;2)z+53 3B3-4;45A-D 2 T(1;2)z+57 | 3C1-3;41A-B;54B-C ( 1 = Gans, 1953, Bull. Biol. Fr. Belg. Supp. 38: 1-90; 2 = Gel- bart, 1971, Ph.D. Thesis, Univ. of Wisconsin. | New order: 1 - 3C1|41A - 21; 20 - 3C3|54B - 41B|54C - 60. # T(1;2)ZWD1 cytology: T(1;2)3C2-5;45C. origin: /-ray-induced. references: Smolik-Utlaut and Gelbart, 1987, Genetics 116: 285-98. genetics: Moles w+ and sterile. # T(1;2)ZWD12 cytology: T(1;2)2A;3C1-2;221A;22A;43F. origin: /-ray-induced. references: Smolik-Utlaut and Gelbart, 1987, Genetics 116: 285-98. genetics: Moles w+ and sterile. #*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)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)N264-100. discoverer: Gersh, 1959. synonym: *T(2;3)100r20. references: 1959, Genetics 44: 163-72. genetics: Selected as a partial reversion from white-mottled. # 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. references: Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1649-70. genetics: Male viable and sterile. #*T(1;2;3)A149 cytology: T(1;2;3)19B1-2;20;48F;81. Complex. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. #*T(1;2;3)b75.1: Translocation (1;2;3) black cytology: T(1;2;3)1B7-8;42E;62B9. new order: 61 - 62B9|1B7-8 - 20; 21 - 42E|1B7-8 - 1A; 60 - 42E|62B9 - 100. origin: X ray induced. references: Ashburner, Faithfull. Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. genetics: Mutant for b (induced by independent event). # T(1;2;3)by35: Translocation (1;2;3) blistery cytology: Break in 3 at 85D7-12 (used to localize by); other breaks not given. origin: X ray induced. references: Kemphues, Raff, Raff, and Kaufman, 1980, Cell 21: 445-51. genetics: Mutant for by. # 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. references: 1970, Genetics 65: 429-48. 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. references: 1970, Genetics 65: 429-48. genetics: Male sterile. Recombination reduced in 2L. #*T(1;2;3)ct268-40: 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)DEB1: Translocation (1;2;3) diepoxybutane cytology: T(1;2;3)20F;24F;88F. origin: Induced by diepoxybutane. references: Denell, Lim, and Auerbach, 1978, Mutat. Res. 49: 219-24. # 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. references: Lindsley, Edington, and Von Halle, 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.|; XR.80 - 61; 60 - 50.81 - 100. Tentative. Postulated that centromere of chromosome 3 split or double with one half capped by 2RD and the other by XRD. XP in the form of a ring. origin: X ray induced. references: Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1649-70. genetics: Variegated for a lethal; male fertile. # T(1;2;3)ML140 cytology: T(1;2;3)20;40-41;80-81. origin: X ray induced. references: Mukhina and Zhimulev, 1980, DIS 55: 209. genetics: Homozygous lethal. #*T(1;2;3)N264-74: 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)N264-87 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 origin: X ray induced. Selected on the basis of pseudolinkage in daughters of treated wild-type males. discoverer: Warters, 1961. new translocation cytology order ( genetics _________________________________________________________________________ T(1;2;3)OR9 19-20;49F;81F 1 male lethal T(1;2;3)OR10 18A;41;73F 2 male viable but sterile T(1;2;3)OR12 3A;41 + 7E;78F 3 male viable but sterile with Y or BSw+Y T(1;2;3)OR14 5E;21D;62C 4 male viable, fertile; homozygous female viable T(1;2;3)OR16 1A;57D + 29;72E 5 male viable but sterile T(1;2;3)OR17 | 20;40-41;61F male viable but sterile T(1;2;3)OR23 14C;27D;87B 6 male lethal T(1;2;3)OR24 14B;39D + 2C;80C + 7 male lethal 29;87A T(1;2;3)OR25 /` 19E;29B;80-81 8 male viable but sterile T(1;2;3)OR26 2D;56F + 3F;96B 9 male viable, fertile T(1;2;3)OR31 - 20;92A + 38D;87E 10 male viable but sterile T(1;2;3)OR34 18F;84B + 28B;75F 11 male lethal + 44C;63A ( 1 = 1 - 19|81F - 61; 20|49F - 60; 21 - 49F|81F - 100. 2 = 1 - 18A|73F - 100; 20 - 18A|41 - 60; 21 - 41|73F - 61. 3 = 1 - 3A|41 - 21; 20 - 7E|78F - 61; 60 - 41|3A - 7E;78F - 100. 4 = 1 - 5E|21D - 60; 20 - 5E|62C - 61; 21A - 21D|62C - 100. 5 = 1A|57D - 21; 20|72E - 61; 60 - 57D|1A - 20|72E - 100. 6 = 1 - 14C|87B - 61; 20 - 14C|27D - 21; 60 - 27D|87B - 100. 7 = 1 - 2C|80C - 87A|19 - 14B|39D - 21; 20 - 19|87A - 100; 60 - 39D|14B - 2C|80C - 61. 8 = 1 - 19E|80 - 100; 20 - 19E|29B - 21; 60 - 29B|80 - 61 (tentative). 9 = 1 - 2D|56F - 21; 20 - 3F|96B - 100; 60 - 56F|2D - 3F|96B - 61. 10 = 1 - 20|92A - 87E|38D - 60; 20|92A - 100; 21 - 38D|87E - 61. 11 = 1 - 18F|84B - 75F|28B - 21; 20 - 18F|84B - 100; 60 - 44C|63A - 75F|28B - 44C|63A - 61 (tentative). | Neither breakpoints in X and 2 with respect to centromere nor new order determined. / Position of breakpoint in chromosome 3 with respect to cen- tromere not determined; therefore new order ambiguous. ` Hyperploid male, presumably carrying XP2LD, survives. - Male hyperploid for XP3RD element survives. # T(1;2;3)S53 cytology: T(1;2;3)2D5;57E;86B. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. csw allele. # T(1;2;3)sc260-18: 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)sc260-29 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)scP1: Translocation (1;2;3) scute of Panshin discoverer: Panshin, 1934. genetics: Mutant for sc. # T(1;2;3)SP: Translocation (1;2;3) from Sao Paulo origin: / ray induced. Selected as male-sterile mutations in y w X chromosome. discoverer: Lindsley and Musatti, 1961. new translocation cytology order ( genetics _________________________________________________________________________ T(1;2;3)SP3 | 20;23A-B;96B 1 male lethal T(1;2;3)SP5 6 break rearrangement: 2 2R (2 breaks), 3L (1 break), 3R (2 breaks) T(1;2;3)SP6 / 20;40-41;80-81 T(1;2;3)SP8 5;17F;44B;90A 3 *T(1;2;3)SP25 ` 19;54;86 4 T(1;2;3)SP29 10E-11A;40;60D;64D 5 T(1;2;3)SP40 4-5;50A;80 + 40;86 6 variegated for a lethal T(1;2;3)SP57 - 20;40-41;75A 7 T(1;2;3)SP65 18A;39E;76A 8 ( 1 = 1 - 20|96B - 61; 20|23A - 21; 60 - 23B|96B - 100. 2 = XD|2RP - 2L; XP|XM|3RM|3LD; 2RD|3LP - 3RP|3RD. 3 = 1 - 5|17F - 20; 21 - 44B|5 - 17F|90A - 100; 61 - 90A|44B - 60. 4 = 1 - 19|54 - 21; 20 - 19|86 - 100; 60 - 54|86 - 61. 5 = 1 - 10E|40 - 60D|64D - 61; 20 - 11A|60D - 60F; 21 - 40|64D - 100. 6 = 1 - 4|80 - 86|40 - 21; 20 - 5|50A - 60; 61 - 80|50A - 40|86 - 100 (tentative). 7 = 1 - 20|75A - 100; 20|40 - 21; 60 - 40|75A - 61 8 = 1 - 18A|76A - 100; 20 - 18A|39E - 21; 60 - 39E|76A - 61. | Male hyperploid for XP2LD element survives. / Neither breakpoints with respect to centromere nor new order determined. ` Male hyperploid for XP3RD element apparently survives. - Breakpoint in chromosome 2 inferred from genetic data. # T(1;2;3)TE35A-100 cytology: T(1;2;3)?;25F;35B;40;?. new order: 21 - 25F|het; het|35B - 40|het; het|25F - 35B|het; origin: / ray induced. discoverer: Samkange. synonym: T(1;2;3)TE146-100. #*T(1;2;3)vL8 cytology: T(1;3)3E5;62D + T(1;2)9D3-4;10A1-2;25E-F. new order: 1 - 3E5|62D - 100; 20 - 10A2|25E - 21; 60 - 25F|9D3 - 3E5|62D - 61. Deficient for 9D4-10A1. origin: X ray induced. references: Lefevre, 1969, Genetics 63: 589-600. genetics: Deficient for ras-v. #*T(1;2;3)wm258-44: 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)wm258-44 may be separated into T(1;3)wm258-44 = T(1;3)3C3-4;4D2-E1;80D, which is deficient for 3C4 through 4D2 (i.e., Df(1)wm258-44 = Df(1)3C3-4;4D2-E1), and Dp(1;2)wm258-44 = 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)wm258-44 should be viable. #*T(1;2;3)wy274-2: 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)yR1: Translocation (1;2;3) yellow of Roberts cytology: T(1;2;3)1B4-8;12F;21D2;41;97F. origin: X ray induced. synonym: T(1;2;3)y-1. references: Roberts, 1974, Mutat. Res. 22: 139-44. genetics: Mutant for y. Male viable and fertile. # T(1;2;3)yR8 cytology: T(1;2;3)1A6-B1;47A;67D. origin: X ray induced. synonym: T(1;2;3)y-8. references: Roberts, 1974, Mutat. Res. 22: 139-44. genetics: Mutant for y and a male lethal not covered by y+Y or l(1)1Ac+Y. # T(1;2;3)z+12E7 cytology: T(1;2)2B12;3C2-5;22A1;24D2 + T(1;3)2B13;80-81. references: Gans, 1953, Bull. Biol. Fr. Belg. Supp. 38: 1-90. genetics: Phenotype z+. # T(1;2;3)z+16G1 cytology: T(1;2;3)3B2-C1;46F2-3;70A. references: Gans, 1953, Bull. Biol. Fr. Belg. Supp. 38: 1-90. genetics: Phenotype z+. # 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)v454. Male sterile. # T(1;2;4)429.28 cytology: T(1;2;4)5B;56D-E;101B-C. new order: 1A - 5B|56D - 21A; 60F - 56E|101B - 101A; 102F - 101C|5B - 20F. discoverer: Gelbart. #*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 hyper- ploid for the XPXD element [i.e., Dp(1;f)A12 = Dp(1;f)1B- C;13B1-5] survives and is claimed to be fertile. Female hyperploid for XM [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)N264-85: 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.)] (complex). new order: 1 - 3B4|60A4 - 21; 20 - 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)N264-85 = Dp(1;4)3B4-C1;6A2-B1;101F-102A viable in both sexes and sterile in male. Complementary Df(1)N264-85 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 XP4D element. #*T(1;2;4)wmbwV: 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)wvD2: 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;101A; 20 - 18F|3C5 - 18F|38 - 21; 60 - 38|101A;101C-102F. 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 cri- terion for postulating break in 4L. Fly hyperploid for the 4PXD element survives. # T(1;2;4)yR29 cytology: T(1;2;4)1E4-F1;20;26A;35B-C;101. origin: X ray induced. references: Roberts, 1974, Mutat. Res. 22: 139-44. genetics: Mutant for y although breakpoint given is proximal to y. Male viable but sterile. # T(1;2;4)z+4E7 cytology: T(1;2;4)3C7-9;56C4-D1;102A. references: Gans, 1953, Bull. Biol. Fr. Belg. Supp. 38: 1-90. genetics: Phenotype z+. # T(1;3)2B7 cytology: T(1;3)2B7;84A4-6. references: Belyaeva, Aizenzon, Semeshin, Kiss, Koczka, Bar- itcheva, Gorelova, and Zhimulev, 1980, Chromosoma 81: 281- 306. #*T(1;3)3 origin: X ray induced. discoverer: Bonner, 1931. references: Dobzhansky, 1935, Z. Indukt. Abstamm. Vererbungsl. 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 chro- mosome 3 in translocation heterozygote normal between es and ro and reduced to two-thirds normal between ro and ca. Male carrying the 3PXD 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)3Ac59 cytology: T(1;3)3A4-6;94F. origin: Induced by triethylenemelamine. synonym: T(1;3)zw1214. references: Lim and Snyder, 1974, Genet. Res. 24: 1-10. genetics: Associated with l(1)3Ac59 (= l(1)zw1214). # T(1;3)3C1 cytology: T(1;3)3C1;81-82. origin: X ray induced in In(1)wm51bLwmJR. references: Gersh, 1967, Genetics 56: 309-19. genetics: Males semiviable and sterile, sometimes M-like . # T(1;3)16 cytology: T(1;3)11F1-2;97D3-4. origin: / ray induced simultaneously with In(3LR)Antprv16. references: Duncan and Kaufman, 1975, Genetics 80: 733-52. # T(1;3)16A4 cytology: T(1;3)9E;80 + T(1;3)14F;66A. new order: 1 - 9E|80 - 66A|14F - 9E|80 - 100; 20 - 14F|66A - 61. origin: Induced by ethyleneimine. references: Lim and Snyder, 1968, Mutat. Res. 6: 129-37. genetics: Homozygous lethal. # T(1;3)20A4 cytology: T(1;3)17F;83A;85D. origin: Induced by ethyleneimine. references: Lim and Snyder, 1968, Mutat. Res. 6: 129-37. genetics: Homozygous lethal. # T(1;3)29A2 cytology: T(1;3)2F;91A. origin: Induced by ethyleneimine. references: Lim and Snyder, 1968, Mutat. Res. 6: 129-37. genetics: Homozygous lethal. # T(1;3)33 cytology: T(1;3)20F;91F5-9. origin: X ray induced. references: Ashburner. #*T(1;3)54a: see Tp(1;3)w+54a4 #*T(1;3)54c: see Tp(1;3)w+54c10 # T(1;3)64b: see Tp(1;3)w+64b #*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)67k: see Tp(1;3)w+67k # T(1;3)71b: see Tp(1;3)f+71b # T(1;3)74c: see Tp(1;3)v+74c #*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 XP3LD element survive and are fertile; duplicated for locus of ru but not se, h, car, or bb. #*T(1;3)143-3 origin: X ray induced. discoverer: Neuhaus. synonym: T(1;3)Del143-3. references: Belgovsky, 1941, DIS 15: 16. genetics: Two breaks in the X chromosome (Gershenson), one between sc and br and another near the centromere (Belgovsky, 1941). A break in chromosome 3 is between st and the cen- tromere of 3. The y+ and sc+ loci are then attached to the proximal end of 3L and the distal end of 3L is attached to the centromere of X. Bulk of the X chromosome is lost. #*T(1;3)260-21 cytology: T(1;3)6C;70E-F. origin: X ray induced simultaneously with In(1)y260-21. discoverer: Sutton, 1939. references: 1943, Genetics 28: 210-17. # T(1;3)429.17 cytology: T(1;3)1B;11B;19C-D;67D;77C-D;94D-E;99A. new order: 1A - 1B|11B - 19C|99A - 94E|77C - 67D|19D - 20F; 61A - 67D|77D - 94D|1B - 11B|99A - 100F. discoverer: Gelbart. # T(1;3)A59: see Tp(1;3)f+71b # T(1;3)A125 cytology: T(1;3)18F-19A;83C + In(1)19E-20. origin: X ray induced. discoverer.: Lefevre. genetics: Male lethal. Allele of l(1)20Ac. # T(1;3)Apx: Translocation (1;3) Antennapedix cytology: T(1;3)20D;79F;84B. references: Stepshin and Ginter, 1970, Genetika (Moscow) 6(9): 101-09. genetics: Mutant for Apx. Homozygous lethal and lethal over In(3R)AntpB [Stepshin and Ginter, 1972, Genetika (Moscow) 8(8): 98-104]. Apx clearly an Antp allele. # T(1;3)Awm609e: see T(1;3)wm609e #*T(1;3)B58l: 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, Jpn. J. Genet. 35: 282. genetics: Position effect at B. Male sterile. #*T(1;3)Bb: Translocation (1;3) Bubble cytology: T(1;3)13E;84F (Morgan, Bridges, and Schultz, 1937, Year Book - Carnegie Inst. Washington 36: 301). origin: X ray induced. discoverer: King, 32d. genetics: Associated with Bb. Male sterile. # T(1;3)biD1: Translocation (1;3) bifid cytology: T(1;3)4C5-6;65C3-5. origin: X ray induced. references: Banga, Bloomquist, Brodberg, Pye, Larrivee, Mason, Boyd, and Pak, 1986, Chromosoma 93: 341-46. genetics: Associated with bi, Qd, and omb. Male lethal. # T(1;3)bxd657: Translocation (1;3) bithoraxoid cytology: T(1;3)X;81?;89E. origin: Induced by ethyl methanesulfonate. discoverer: E.B. Lewis. synonym: bxd16765.7. genetics: Associated with bxd657. # T(1;3)C: Translocation (1;3) Crossover suppressor origin: X ray induced. discoverer: Roberts, 1964, 1965. references: 1970, Genetics 65: 429-48. translocation cytology genetics _______________________________________________________________________________ T(1;3)C48 ( In(1)10E-F;18C-D + male lethal; crossing over reduced in X T(1;3)20;80-81 T(1;3)C151 | 9D;80-81 male viable but sterile; crossing over reduced in X T(1;3)C160 | 14B;80-81 male lethal; crossing over reduced in X T(1;3)C195 11D;71A-B male viable and sterile; crossing over reduced in X T(1;3)C250 ( In(1)9F;15D-E + male viable and fertile; homozygous female T(1;3)20;80-81 viable; crossing over reduced in X T(1;3)C291 / 16C;20;87F;98E male viable and fertile; homozygous female viable; crossing over reduced in X T(1;3)C300 ` 12C;61F;66E;68D male dies in 3rd larval instar; crossing over reduced in 3L T(1;3)C315 20;70F male fertile; homozygous female lethal; crossing over reduced in 3L T(1;3)C329 | 3F;80-81 male viable and sterile; crossing over reduced in X ( Presence of T(1;3)20;80-81 inferred from genetic data. | Position of breakpoint in chromosome 3 with respect to cen- tromere not determined. / New order: 1 - 16C|98E - 87F|(16C - 20)|87F - 61; 20|98B - 100. ` New order: 1 - 12C|68D - 100; 61 - 61F|66E - 61F|68D - 66E|12C - 20. # T(1;3)C212 cytology: T(1;3)1A7;2C3;80. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. # T(1;3)C243 cytology: T(1;3)20A3;75C. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. # T(1;3)CA17 cytology: T(1;3)20F;86F. origin: / ray induced. references: Ashburner. genetics: Associated with b80j1. # T(1;3)CA45 cytology: T(1;3)20?;97E. origin: / ray induced. references: Ashburner. genetics: Induced simultaneously with Df(2L)b84a2. #*T(1;3)ct268-5: Translocation (1;3) cut 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)ct268-21 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)ct268-36 cytology: T(1;3)7B2-C1;66F (Sutton). origin: X ray induced. discoverer: Demerec, 39j. genetics: Mutant for ct. Male lethal. # T(1;3)ctJ origin: X ray induced. references: Lefevre and Johnson, 1973, Genetics 74: 633-45. genetics: Male lethal. translocation cytology ___________________________ T(1;3)ctJ2 ( 7B3-4;96A T(1;3)ctJ9 7B3-4;86D-E T(1;3)ctJ11 7B3-4;95F ( Viable over ct71g. Not covered by Dp(1;3)sn13a1. #*T(1;3)cu100.69: 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)DEB: Translocation (1;3) diepoxybutane origin: Induced by diepoxybutane. Selected by pseudolinkage in patroclinous sons of treated males. references: Denell, Lim, and Auerbach, 1978, Mutat. Res. 49: 219-24. genetics: Male fertile. translocation cytology __________________________________ T(1;3)DEB1 20F;80-81 T(1;3)DEB2 20F;97 T(1;3)DEB3 20F;80-81 T(1;3)DEB4 20F;80-81 T(1;3)DEB5 T(1;3)DEB6 20F;62B T(1;3)DEB7 20F;80-81 # T(1;3)Del 143-3: see T(1;3)143-3 # T(1;3)dsx: Translocation (1;3) doublesex origin: X ray induced. references: Baker, Hoff, Kaufman, Wolfner, and Hazelrigg, 1991, Genetics 127: 125-38. genetics: Revertant of dsxM. translocation cytology synonym _________________________________________________________________ T(1;3)dsx33 18D3-5;20F;80-81;84E1-2 T(1;3)dsxM+R12 T(1;3)dsx44 20F;84D13-E8 T(1;3)dsxM+R46 # T(1;3)eH2: Translocation (1;3) ebony of Henikoff cytology: T(1;3)20:93D. origin: X ray induced. references: Henikoff, 1980, DIS 55: 61-62. genetics: Variegated for e in XX and XXY females and XY males; XX flies more ebony than XXY or XY flies. Mutant for e in X0 males. Homozygous lethal. #*T(1;3)f257-29: 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)15D, B, or os. Male viable and sterile. # T(1;3)FA11 cytology: T(1;3)20F;84D-87D. references: Lehmann and Nusslein-Volhard, Dev. Biol. 119: 402-17. # T(1;3)FA62 cytology: T(1;3)19-20;84F-90D. references: Lehmann and Nusslein-Volhard, Dev. Biol. 119: 402-17. # T(1;3)FC8 cytology: T(1;3)20;84D-85D. origin: X ray induced. references: Lehmann and Nusslein-Volhard, 1987, Dev. Biol. 119: 402-17. Agnel, Kerridge, Vola, and Rabinow, 1989, Genes Dev. 3: 85- 95. #*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 32P in In(3R)P. discoverer: Bateman, 1949. references: 1950, DIS 24: 54. 1951, DIS 25: 77. genetics: Associated with fd. # T(1;3)GA origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. translocation cytology mutant for ______________________________________ T(1;3)GA25 3E;80A-B T(1;3)GA79 2F-3A;82C phl T(1;3)GA91 1F4;99A T(1;3)GA119 1E1;93A # T(1;3)GE222 cytology: T(1;3)2B6;83E. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Mutant for br. # T(1;3)GE245 cytology: T(1;3)3C7;96. Region from 80-96 complex. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. N allele. #*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)h+06 cytology: T(1;3)1B10-C1;66D14-E1. origin: X ray induced. references: Jeffery, 1979, Genetics 91: 105-25. genetics: Male viable but sterile. Variegates for h. # T(1;3)HA14 cytology: T(1;3)19E;80. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. run allele. # T(1;3)JA29 cytology: T(1;3)1E5;85A. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. # T(1;3)JC59 cytology: T(1;3)2F6-3A1;92F-93A. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Mutant for phl. # T(1;3)JC153: see Tp(1;3)JC153 # T(1;3)JK: Translocation (1;3) Jim Kennison cytology: T(1;3)Xh;80. origin: / ray induced. discoverer: Kennison. translocation genetics ___________________________________________________________ T(1;3)JK1 male viable and fertile; variegates for Pc4 T(1;3)JK2 male lethal T(1;3)JK3 male lethal T(1;3)JK4 male semi-lethal T(1;3)JK5 male viable, but sterile T(1;3)JK6 male viable and fertile # T(1;3)K2: see Dp(1;3)K2 #*T(1;3)KA12 cytology: T(1;3)19E;95D. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of l(1)19Ec. #*T(1;3)l-184: Translocation (1;3) lethal cytology: T(1;3)18A;81. origin: X ray induced. references: Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1649-70. genetics: Associated with *l(1)184. # T(1;3)l-v3: Translocation (1;3) lethal-variegated origin: X ray induced. references: Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1649-70. genetics: Variegated for a lethal; male sterile. Survival of X/Y males much greater than that of X/O males. translocation cytology ______________________________________ T(1;3)l-v3 4A;81 T(1;3)l-v163 ( 17A-B;80-81 *T(1;3)l-v252 *T(1;3)l-v361 | 19-20;80-81 T(1;3)l-v453 ( 12D;80-81 T(1;3)l-v455 / 3C;81 T(1;3)l-v463 | 19-20;81-82 ( Position of chromosome 3 breakpoint with respect to centromere not determined. | Position of breakpoints with respect to centromere not deter- mined. / Also variegated for w. # T(1;3)L1: see T(1;3)vL1 #*T(1;3)lz268-29: 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)lz268-29/lz female fertile. Male lethal. # T(1;3)M: Translocation (1;3) Mglinetz translocation cytology origin ref ( _______________________________________________ T(1;3)M50 20;87E / ray 2 T(1;3)M149 8C;86A / ray 1 T(1;3)M150 6B;90E / ray 1 T(1;3)M152 12A;91F / ray 1 T(1;3)M153 7F;100A / ray 1 T(1;3)M155 3A;97A / ray 1 T(1;3)M159 3F;84E 32P feeding 1 T(1;3)M160 19D;99B 32P feeding 1 T(1;3)M161 3A;64A 32P feeding 1 T(1;3)M162 10B;67E 32P feeding 1 T(1;3)M163 8E;71E 32P feeding 1 ( 1 = Mglinetz, 1968, Genetika (Moscow) 4(8): 81-86; 2 = Mglinetz, 1972, Genetika (Moscow) 8(2): 82-92. #*T(1;3)N34b: 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. other information: Reported as suspected of being a T(1;3); basis of suspicion not given. # T(1;3)N81k9 cytology: T(1;3)3C6-9;3L (Welshons). origin: X ray induced. discoverer: Muscavitch. references: Grimwade, Muskavitch, Welshons, Yedvobnick, and Artavanis-Tsakonas, 1985, Dev. Biol. 107: 503-19. genetics: Mutant for N. molecular biology: Molecular breakpoint 24.2 to 22.6 kb to the left of the In(1)N76b8 breakpoint (Grimwade et al., 1985). #*T(1;3)N264 origin: X ray induced. discoverer: Demerec. new translocation cytology order ( ref | genetics ______________________________________________________________________________ *T(1;3)N264-29 / 3D4-5;80 (Hoover) 1 rstv fav dmv *T(1;3)N264-34 3C3-5;70C2-3 (Hoover) 1 N *T(1;3)N264-55 3D4-5;80F9-81F1 1 wv rstv fav dmv *T(1;3)N264-56 3D4-5;80 (Sutton) wv Nv (probably) *T(1;3)N264-64 3E5-6;80C-F (Hoover) 1 wv rstv fav dmv *T(1;3)N264-65 2B10-16;3D4-5; 1 wv rstv fav dmv 81E;96C4-5 *T(1;3)N264-70 3C4-5;80D-F + 6F2-7A1; 2 2 wv rstv fav dmv 100B2-3 *T(1;3)N264-83 3C6-7;12F2-4;79E2-3 + 3 1 N In(3R)81;88 *T(1;3)N264-104 3C7-9;87D1-E1 + 4 svr N In(1)B4-5;18-19 *T(1;3)N264-121 3C7-9;81F;86B6-C1 5 N ( 1 = 1 - 2B10|(81F - 96C4)|3D5 - 20; 61 - 81F|(2B16 - 3D4)|96C5 - 100. 2 = 1 - 3C4|80F - 100B2|6F2 - 3C5|80D - 61; 20 - 7A1|100B3 - 100F. 3 = 1 - 3C6|12F2 - 3C7|79E3 - 81|88 - 81|88 - 100; 20 - 12F3|79E2 - 61. 4 = 1A1 - 1B4|18 - 3C9|87D1 - 61; 20 - 19|1B5 - 3C7|87E1 - 100. 5 = 1 - 3C7|81F - 86B6|81F - 61; 20 - 3C9|86C1 - 100. | 1 = Demerec, 1941, Proc. Int. Congr. Genet. 7th, pp. 99-103; 2 = Sutton, 1940, Genetics 25: 534-40. / X/Y male lethal; X/Y/Y male occasionally survives. # T(1;3)N3 cytology: T(1;3)1E1;71C1 and other rearrangements (complex). origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. # T(1;3)N72 cytology: T(1;3)7D;61F. origin: X ray induced. discoverer: Lefevre. references: Digan, Haynes, Mozer, Dawid, Forquignon, and Gans, 1986, Dev. Biol. 114: 161-69. genetics: Allele of fs(1)h. Male lethal. molecular biology: Lesion associated with the 7D breakpoint lies between 50.6 and 51.4 kb. # T(1;3)npr1: Translocation (1;3) nonpupariating1 cytology: T(1;3)2B5;61F3-4. origin: Induced by DEB. synonym: npr17; nprJTD3. references: Kiss, Beaton, Tardiff, Fristrom, and Fristrom, 1988, Genetics 118: 247-59. genetics: Mutant for npr1. # 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)OR: Translocation (1;3) from Oak Ridge origin: X ray induced. Selected by virtue of pseudolinkage displayed by daughters of treated males. discoverer: Warters, 1961. new translocation cytology order ( genetics ________________________________________________________________________ T(1;3)OR1 | 5A;20;66B;79E 1 male lethal T(1;3)OR6 4D;87F male viable but sterile T(1;3)OR7 14D;91E male viable but sterile T(1;3)OR9 6D;66B variegated for a lethal; males sterile with small rough eyes T(1;3)OR11 18F;84B male viable but sterile T(1;3)OR12 / 2B6-13;84A + 2 male viable but sterile 18D;98F-99A (Becker) T(1;3)OR13 15A;84E male viable but sterile T(1;3)OR14 17A;80B variegated for a lethal; male sterile T(1;3)OR15 18D;88A male viable but sterile; male lethal acquired later T(1;3)OR17 | 19E;67C male viable, fertile; homozygous female viable T(1;3)OR18 19B;80A male viable but sterile T(1;3)OR19 12E;75F male viable but sterile T(1;3)OR21 | 19E;61F male viable but sterile; XO male lethal T(1;3)OR22 6C;98C male viable, fertile; homozygous female viable T(1;3)OR23 ` 20;80-81 male viable but sterile T(1;3)OR24 12F;80B male viable but sterile T(1;3)OR25 / 20B;99B male viable but sterile T(1;3)OR28 11A;80C male lethal T(1;3)OR29 16F;84B male viable but sterile T(1;3)OR30 | 19E;65D male viable but sterile T(1;3)OR31 10A;68D male viable but sterile T(1;3)OR32 16A;71B male viable but sterile T(1;3)OR33 13E;62F male virtually lethal T(1;3)OR34 3A;65A male viable but sterile with Y or BSw+Y T(1;3)OR35 19E;75C male viable but sterile T(1;3)OR36 7D;62A;87E 3 male viable but sterile T(1;3)OR37 3C;97F male viable, fertile; homozygous female viable T(1;3)OR38 | 18D;61D male viable but sterile T(1;3)OR39 6B-F;75C male viable but sterile T(1;3)OR40 6F;62D + 4 male viable but sterile 16B;20;84F T(1;3)OR41 9F;98E male viable but sterile T(1;3)OR43 / 20A;97D male viable but sterile T(1;3)OR45 17A;61D male viable but sterile T(1;3)OR46 12C;80A variegated for a lethal; male sterile T(1;3)OR47 / 20;93D male viable, fertile; homozygous female viable T(1;3)OR49 11A;66D male viable but sterile T(1;3)OR51 12D;97A male lethal T(1;3)OR52 19E;70C;83F 5 male viable but sterile T(1;3)OR54 12F;83A male lethal *T(1;3)OR55 11C;67C male viable but sterile *T(1;3)OR57 3E;5B;61C 6 male lethal even with BSw+Y T(1;3)OR59 ` 20;80-81 male lethal T(1;3)OR60 4B;88A male lethal T(1;3)OR62 10F;88C male viable but sterile T(1;3)OR63 ` 20;80-81 male sterile T(1;3)OR66 3F;71E male lethal even with BSw+Y T(1;3)OR67 4C;73C male viable but sterile T(1;3)OR69 ` 20;80-81 male viable but sterile T(1;3)OR71 20;71D male viable but sterile T(1;3)OR72 ` 20;80-81 variegated for a lethal; male sterile ( 1 = 1 - 5A|79E - 66B|5A - 20|79E - 100; 20|66B - 61. 2 = 1 - 2B6|84A - 98F|18D - 2B13|84A - 61; 20 - 18D|99A - 100 (tentative). 3 = 1 - 7D|62A - 87E|62A - 61; 20 - 7D|87E - 100. 4 = 1 - 6F|62D - 84F|20 - 16B|84F - 100; 20|16B - 6F|62D - 61. 5 = 1 - 19E|83F - 70C|83F - 100; 20 - 19E|70C - 61 (tentative). 6 = 1 - 3E|5B - 3E|61C - 100; 20 - 5B|61C - 61A. | Male hyperploid for XP3LD survives. / Male hyperploid for XP3RD survives. ` Positions of breakpoints with respect to centromere not deter- mined. # T(1;3)osbdw: 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 osbdw. Male sterile. # T(1;3)P104: Translocation (1;3) Pasadena cytology: T(1;3)19-20;87F-88A. origin: X ray induced. discoverer: E.B. Lewis. # T(1;3)pn12: Translocation (1;3) prune cytology: T(1;3)2E1-2;98A1-2. origin: X ray induced. references: Ilyina, Sorokin, Belyaeva, and Zhimulev, 1980, DIS 55: 205. genetics: Mutant for pn. Male lethal. # T(1;3)pn36 cytology: Tp(3;1)2E1-2;61A;62C1-2. new order: 1A|62C3 - 100; 61A - 62C2|2E1 - 1A|2E2 - 20. Tentative. origin: X ray induced. references: Ilyina, Sorokin, Belyaeva, and Zhimulev, 1980, DIS 55: 205. genetics: Mutant for pn. # T(1;3)rbD1: Translocation (1;3) ruby cytology: T(1;3)4C6-7;3R. origin: X ray induced. references: Banga, Bloomquist, Brodberg, Pye, Larrivee, Mason, Boyd, and Pak, 1985, Chromosoma 93: 341-46. genetics: Associated with rb. Male lethal. # T(1;3)RF29 cytology: T(1;3)3D;7D4;93F-94A + complex autosomal rearrange- ment. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Mutant for dm. Female fertile over FM6 (Lefevre). #*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)sc260-15: 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)sc260-20 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 homoz- ygous female viable and fertile. The two halves of the translocation are recoverable independently. The XP3D element should be deficient for y and ac but carry sc260-20; it presumably is male lethal but survives in heterozygous female. The 3PXD element carries normal alleles of y and ac but not sc260-20 or svr+ and should also carry normal alleles of ve and ru. # T(1;3)scJ4: 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 subse- quently separated from the rest of the configuration and was lost. Base of the X, presumably capped by the undemonstrable terminus of 3L (i.e., XP3D), 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 4PXD element from T(1;4)wm5 or Dp(1;f)z9. The 3PXD segregant carries normal alleles of l(1)Ac, 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)scJ4 restores viability of In(1)scV2/0 males (Baker, 1971, Proc. Nat. Acad. Sci. USA 68: 2472-76). #*T(1;3)scK: Translocation (1;3) scute of Krivshenko discoverer: Krivshenko. references: Agol, 1936, DIS 5: 7. genetics: Mutant for sc. Three-break rearrangement with XD translocated to 3LP, 3LD translocated to 3RP and 3RD translocated to XP. # T(1;3)scK3 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. 3PXD element is viable homozygous, although males are somewhat infrequent. XP3D is inviable in males and homozygous females but survives in heterozygous females. # T(1;3)scKA8 cytology: T(1;3)1B4-5;98+. discoverer: Lefevre. references: Carramolino, Ruiz-Gomez, Guerrero, Campuzano, and Modolell, 1982, EMBO J. 1: 1185-91. genetics: Mutant for sc. molecular biology: X breakpoint between coordinates +13.7 and +16.7 (Carramolino et al., 1982). # T(1;3)ShLC: Translocation (1;3) Shaker cytology: T(1;3)16F1-2;80. origin: X ray induced. references: Tanouye, Ferrus, and Fujita, 1981, Proc. Nat. Acad. Sci. USA 78: 6548-52. Papazian, Schwartz, Tempel, Jan and Jan, 1987, Science 237: 749-53. genetics: Associated with Sh15. molecular biology: Maps to a HindIII-EcoRI fragment between +54.1 and +59.1 kb (Kamb, Iverson, and Tanouye, 1987, Cell 50: 405-13) or +53 to +55 kb (Bauman, Krah-Jentgens, Muller, Muller-Holtkamp, Seidal, Keckemethy, Casal, Ferrus, and Pongs, 1987, EMBO J. 6: 3419-29). # T(1;3)slu: Translocation (1;3) sluggish cytology: T(1;3)2E;97A10. origin: / ray induced. references: Sharma, 1977, Experientia 33: 171-73. genetics: Males (semifertile) show abnormal phototactic behavior and light-dependent homosexual activity. Homozygous females sluggish and sterile. No crossing over reported in heterozygous females. Mutant phenotype recessive. # T(1;3)SMG: Translocation (1;3) Semenova Mglinetz Glotoff cytology: T(1;3)11A;70E. origin: / ray induced. references: Semenova, Mglinetz, and Glotoff, 1970, Genetika (Moscow) 6(4): 165-69. # T(1;3)SP: Translocation (1;3) from Sao Paulo origin: / ray induced. Selected as male-sterile mutations in a y w X chromosome. discoverer: Lindsley and Musatti, 1961. genetics: Male viable but sterile. translocation cytology ________________________________ *T(1;3)SP2 20;90E T(1;3)SP11 20;75B T(1;3)SP13 ( 20;80-81 T(1;3)SP14 ( 20;80-81 *T(1;3)SP15 | 20;67 T(1;3)SP21 1B;83F T(1;3)SP22 ( 20;80-81 T(1;3)SP26 ( 20;80-81 T(1;3)SP34 8A;84A T(1;3)SP37 8F;64E T(1;3)SP38 / 10B10-12;85A8-12 T(1;3)SP41 3E;67C-D T(1;3)SP44 ( 20;80-81 T(1;3)SP46 11;98 T(1;3)SP53 12;92 T(1;3)SP54 | 20;67B T(1;3)SP59 20;83C T(1;3)SP62 20;89A T(1;3)SP63 | 20;65 T(1;3)SP68 11A;80-81 T(1;3)SP70 ( 20;80-81 *T(1;3)SP73 ` 20;89E T(1;3)SP79 13D;64A *T(1;3)SP80 - 18C;100A T(1;3)SP82 5B-C;81 T(1;3)SP85 16B;80-81 T(1;3)SP90 18D;68A T(1;3)SP96 T(1;3)SP99 12E;64E T(1;3)SP109 T(1;3)SP112 11B;85D T(1;3)SP122 11E;92E T(1;3)SP123 ( Positions of breakpoints with respect to centromere not deter- mined. | Male hyperploid for XP3LD element survives. / Lefevre, 1970, DIS 45: 39. ` Mutant for Ubx. - Male hyperploid for XP3RD element survives. Position of chromosome 3 breakpoint with respect to centromere not determined. # T(1;3)Tabrv175: Translocation (1;3) Transabdominal-reverted cytology: T(1;3)20;89E + In(3R)89F;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, abnormal posterior spiracles and a rudimentary ninth ventral setal band. # T(1;3)Th1: Translocation (1;3) from Thymidine cytology: T(1;3)12C;65B. origin: From male treated with 3H-thymidine as larva. discoverer: Kaplan. genetics: Male lethal. # T(1;3)Uab5: Translocation (1;3) Ultraabdominal cytology: T(1;3)1F;89E3-4. origin: Induced by ethyl methanesulfonate. references: Lewis, 1978, Nature 276: 565-70. genetics: Phenotype associated with the distal part of the translocation; break in 89E to left of Uab5 and to right or left of iab2. # T(1;3)Ubx: Translocation (1;3) Ultrabithorax genetics: Associated with Ubx. translocation cytology origin discov. synonym ____________________________________________________________ T(1;3)Ubx8A 5B;89E1-2 Ubx21560.8A T(1;3)UbxR49 20F;89E X ray Ramey CbxrevR17.49A T(1;3)UbxX-A 20;89E # T(1;3)v: Translocation (1;3) vermilion cytology: T(1;3)10A1-2;93B7-10 (Lefevre, 1970). origin: X ray induced in a chromosome carrying v. discoverer: Anderson, 1924. references: 1925, Papers Mich. Acad. Sci. 5: 355-66. 1926, Papers Mich. Acad. Sci. 7: 273-78. 1929, Z. Indukt. Abstamm. Vererbungsl. 51: 397-411. Lefevre, 1970, DIS 45: 39. Zhimulev, Belyaeva, Khudyakov, and Pokholkova, 1980, DIS 55: 211. Zhimulev, Pokholhova, Bgatov, Semeshin, and Belyaeva, 1981, Chromosoma 82: 25-40. genetics: Inseparable from v. Male viable and sterile. Male sterility associated with loss of central pair of microtubules from sperm-tail axoneme [Kiefer, 1973, Genetic Mechanisms of Development (F.H. Ruddell, ed.). Academic Press, New York, London, San Francisco, pp. 47-102]. 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)vL1 cytology: T(1;3)3E1-2;90C9-11 + Df(1)10A1-2;10A4-5 (separable). origin: X ray induced. synonym: T(1;3)L1. references: Lefevre, 1969, Genetics 63: 589-600. Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Khu- dyakov, Patzevich, Semeshin, Baricheva, Aizenzon, Kramers, and Eeken, 1982, DIS 58: 210-14. genetics: Deficient for v-l(1)10Ac. # T(1;3)vL13 cytology: T(1;3)9B13-14;10A1-2;64F. origin: X ray induced. references: Lefevre, 1969, Genetics 63: 589-600. genetics: Mutant for v. Male lethal. # T(1;3)V5-2: Translocation (1;3) Valencia cytology: T(1;3)13A8-9;84E. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. genetics: Male sterile. # T(1;3)V105 cytology: T(1;3)12D3;81. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. genetics: Male sterile. #*T(1;3)Vel: Translocation (1;3) Velvet origin: X ray induced in In(1)sc8. discoverer: Patterson. references: 1934, DIS 2: 10. genetics: Associated with Vel. Homozygous viable and fertile. # T(1;3)wDZL: Translocation (1;3) white cytology: T(1;3)3C1-2;3L. origin: In a wDZL/wDZL female. Presumed to be a rearrangement generated by wDZL. references: Bingham, 1980, Cold Spring Harbor Symp. Quant. Biol. 45(2): 519-25. genetics: T(1;3)wDZL/wDZL females have wild-type eye color. #*T(1;3)wm1: 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 males lethal; X/Y/Y males viable and sterile. other information: First recorded case of variegated position effect. #*T(1;3)wm2 origin: X ray induced. discoverer: Patterson. references: Muller, 1930, J. Genet. 22: 299-334. genetics: Variegated for w. Male sterile. #*T(1;3)wm258-32 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)wm258-44 cytology: T(1;3)3C3-4;4D2-E1;80D; deficient for 3C4-4D2. origin: Aneuploid segregant from T(1;2;3)wm258-44/+. #*T(1;3)wm258-54 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)wm264-58: see T(1;3)N264-58 #*T(1;3)wm609e cytology: T(1;3)3C2-3;100C3-7. origin: X ray induced. discoverer: Patterson. synonym: T(1;3)Awm609e. references: Griffen and Stone, 1938, Genetics 23: 149. genetics: Variegated for w. Seems likely that the rearrange- ment is more complicated because a euchromatic-euchromatic translocation would not be expected to produce variegation. # T(1;3)wmSp: see Tp(1;3)wm49a # T(1;3)Wrv19: Translocation (1;3) Wrinkled-reverted cytology: T(1;3)18F3-5;75C3-7. origin: X ray induced. discoverer: Faithfull. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou and Woodruff, 1980, DIS 55: 193-95. genetics: Induced revertant of W. # T(1;3)X1ts cytology: T(1;3)8C1-2;91D1-2. origin: / ray induced. references: Kaufman and Suzuki, 1974, Can. J. Genet. Cytol. 16: 579-92. genetics: Temperature-sensitive lethal. Male sterile at all temperatures. Lethal phenotype maps (by duplications) to 7C9-9D4. # T(1;3)X3ts cytology: T(1;3)10E1-2;92F12-13. origin: / ray induced. references: Kaufman and Suzuki, 1974, Can. J. Genet. Cytol. 16: 579-92. genetics: Temperature-sensitive lethal, leaky at 29. Male sterile at all temperatures. # T(1;3)y67k5: Translocation (1;3) yellow cytology: T(1;3)1B1-2;98C. origin: X ray induced. discoverer: Lefevre, 67k5. references: 1970, DIS 45: 32. genetics: Male viable, fertile, and y. #*T(1;3)y260-11 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)y260-21 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)yA78j cytology: T(1;3)1B1-2;82A1. origin: / ray induced. references: Alexandrov, Ankina, and Alexandrova, 1985, DIS 61: 212-13. genetics: Mutant for y. # T(1;3)yR19 cytology: T(1;3)1A5-1B1;87A. origin: X ray induced. references: Roberts, 1974, Mutat. Res. 22: 139-44. genetics: Male viable, fertile, and y. # T(1;3)yR26 cytology: T(1;3)17C;70C. origin: X ray induced. references: Roberts, 1974, Mutat. Res. 22: 139-44. genetics: Male viable but sterile. Body color y although break at proximal end of the X, independent of y locus. # T(1;3)z+: Translocation (1;3) zeste-wild type origin: X-ray-induced rearrangements of z-bearing X chromosomes that interfere with z-w interaction. genetics: z+ phenotype. translocation cytology ref ( ________________________________________________________ T(1;3)z+7E8 3C6-7;75A2-3;85F-86A;93C-93E 1 T(1;3)z+9 3C;84A 2 T(1;3)z+12G2 3C1-2;93F2-4 1 T(1;3)z+13E8 2F2;3C3-5;13D2-F4;96F2-4;97A3-B1 1 T(1;3)z+13 3C2-3;85D-E 2 T(1;3)z+14 3C1-2;75B-C 2 T(1;3)z+15 1B4-9;83F2-4 + 2 In(1)4D-5A;12A-B T(1;3)z+19G3 3C1-2;71D + other 1 autosomal breaks T(1;3)z+21 3C1-2;4C4-6;72A-F + 2 T(1;3)8A-F;75-76 T(1;3)z+22 3C3-5;71A-C 2 T(1;3)z+26 3C3-5;80-81 2 ( 1 = Gans, 1953, Bull. Biol. Fr. Belg. Supp. 38: 1-90; 2 = Gel- bart, 1971, Ph.D. Thesis, Univ. of Wisconsin. # T(1;3)z7: Translocation (1;3) zeste cytology: T(1;3)3D3-4;100D1-2. origin: X ray induced in z w+ X chromosome. references: Gans, 1953, Bull. Biol. Fr. Belg. Suppl. 38: 1-90. Jack and Judd, 1979, Proc. Nat. Acad. Sci. USA 76: 1368-72. genetics: Eye color zeste in z w+ males carrying the duplica- tion. # T(1;3)zw1214: see T(1;3)3Ac59 # T(1;3)ZWD origin: /-ray-induced in a z1-bearing X chromosome. references: Smolik-Utlaut and Gelbart, 1987, Genetics 116: 285-98. translocation cytology genetics _________________________________________________________ T(1;3)ZWD6( 3C;67F + 20;90D w+ sterile + In(1)11E;19E males T(1;3)ZWD9 3C1;98D w+ males, z females T(1;3)ZWD15| 3C1-2;75F + 11A;88E male lethal New order: 1A - 3C|67F - 90D|20 - 19E|11E - 19E|11E - 3C|67F - 61A; 20|90D - 100F. New order: 1A - 3C1|75F - 88E|11A - 3C2|75F - -61A; 20 - 11A|88E - 100F. #*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|chrom3P; 20 - 3C7|101F - 102F; chrom3D|101F - 101A. origin: X ray induced. discoverer: Mackensen. references: 1935, J. Heredity 26: 163-74 (fig.). genetics: Variegated for w. # T(1;3;4)R45 cytology: T(1;3;4)X;61C3-4;101A-C. references: Gelbart, 1971, Ph. D. Thesis, Univ. of Wisconsin. # T(1;3;4)Tabrv114 cytology: T(1;34)20;89E;101 + 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, abnormal posterior spiracles and a rudimentary ninth ventral setal band. molecular biology: Lesion associated with the 89E breakpoint lies between 183 and 184 kb. # T(1;4)1: see T(1;4)BS #*T(1;4)1: see Tp(1;4)A1 #*T(1;4)3A: see T(1;3;4)A # T(1;4)4: see T(1;4)BS # T(1;4)4C3 cytology: T(1;4)4C3;101-102. discoverer: Lindsley. references: Hawley, 1980, Genetics 94: 625-46. #*T(1;4)231b origin: X ray induced. discoverer: Patterson. references: Patterson and Painter, 1931, Science 73: 530-31. Patterson, 1932, Am. Nat. 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)A: Translocation (1;4) Austin origin: X ray induced. translocation cytology discoverer ref ( __________________________________________________________________________________ *T(1;4)A2 X.4 2,5,10 *T(1;4)A3 10% of X transferred Patterson, 301 2,4,6,7 to 4 *T(1;4)A4 13F6-14A1 2,3,8,9,10,11 *T(1;4)A5 X.4 2,5,12 *T(1;4)A6 X.4 2,5,12 *T(1;4)A7 X.4 2,5,12 *T(1;4)A8 11A6-7 2,8,9,10,11,12 T(1;4)A9 5A1-4 2,8,9,10,11,12 *T(1;4)A10 1A5-6;102A2-4 2,10,12,13 *T(1;4)A11 X.4 1,2,5,12 T(1;4)A13 18C5-D1 2,8,9,10,11,12 T(1;4)A14 X.4 1,2,5,12 T(1;4)A17 | 7F5-8A2 Mickey 2,9,11 ( 1 = Brown, 1940, Texas Univ. Publ. 4032: 65-72; 2 = CP627; 3 = Mackensen, 1935, J. Hered. 26: 163-74; 4 = Muller and Painter, 1932, Z. Indukt. Abstamm. Vererbungsl. 62: 316-65; 5 = Painter and Stone, 1935, Genetics 20: 327-41 (fig.); 6 = Patterson, 1932, Genetics 17: 38-59; 7 = Patterson and Painter, 1931, Science 73: 530-31; 8 = Patterson, Stone, and Bedichek, 1935, Genetics 20: 259-79 (fig.); 9 = Patterson, Stone, and Bedichek, 1937, Genetics 22: 407-26; 10 = Patter- son, Stone, Bedichek, and Suche, 1934, Am. Nat. 68: 359-69; 11 = Pipkin, 1940, Texas Univ. Publ. 4032: 126-56; 12 = Stone, 1934, Genetica 16: 506-20; 13 = Stone and Griffen, 1940, Texas Univ. Publ. 4032: 208-17; | X chromosome broken between t and lz, although the reported cytological breakpoint is to the left of this interval. The 4PXD 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 XP4D 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)A4: see T(1;4)BS # T(1;4)A5: see T(1;4)wm5 # T(1;4)B68f cytology: T(1;4)15F;101 (chromocenter). origin: X ray induced. references: Brosseau, 1969, DIS 44: 45. genetics: Associated with B68f, a moderate allele of Bar. Male viable but sterile. # T(1;4)BS: 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 - 101F; 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. Novitski, 1970, DIS 45: 87. Childress and Hartl, 1972, Genetics 71: 417-27. genetics: Position effect at B more extreme than in Dp(1;1)B. Homozygous female viable and fertile. Male also viable but with reduced fertility (Novitski, 1970). The XP4D segregant carries no known markers from chromosome 4 and BS through bb+ from X. Female hyperploid for this element viable and fer- tile. Hyperploid male poorly viable and sterile. other information: Used by Stern in cytological demonstration of crossing over (1931, Biol. Zentr. 51: 547-87). XP4D from T(1;4)BS used by Lindsley and Sandler [1963, Methodology in Basic Genetics (W. J. Burdette, ed.). Holden-Day, Inc., pp. 390-403] in construction of compound-generating BS dupli- cations. Reciprocal products of meiosis in male not recovered with equal frequencies (Novitski and Sandler, 1957, Proc. Nat. Acad. Sci. USA 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; Novitski, 1970, DIS 45: 87). # T1;4)e15 cytology: T(1;4)13C;101-102. references: McKee, 1987, Genetics 116: 409-13. #*T(1;4)HF346 cytology: T(1;4)2C1-2;101. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. # T(1;4)JC43 cytology: T(1;4)3B1-2;3E3-4;102D (Lefevre). new order: 1A - 3B1|102D - F; 101A - 102D|3E3 - 3B2|3E4 - 20. origin: X ray induced. discoverer: Lefevre. references: Young and Judd, 1978, Genetics 88: 723-42. Smith and Konopka, 1981, Mol. Gen. Genet. 183: 243-51. Reddy, Zehring, Wheeler, Pirotta, Hadfield, Hall, and Rosbach, 1984, Cell 38: 701-10. genetics: Male lethal. X break near per; disrupts normal expression of gene (Reddy et al., 1984). molecular biology: 3B1-2 breakpoint is approximately 100 kb distal to the wa copia insertion point (Pirrota, Hadfield, and Pretorius, 1983, EMBO J 2: 927-34; Reddy et al., 1984). # T(1;4)l-v11: Translocation (1;4) lethal-variegated cytology: T(1;4)15;101. origin: X ray induced. references: Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1649-70. genetics: Variegated for a lethal. Male fertile. # T(1;4)m5: see T(1;4)wm5 #*T(1;4)M-pro: Translocation (1;4) Minute-producer discoverer: Bridges, 33d26. synonym: M-pro: Minute-producer. genetics: Minutes produced are haplo-4's. The translocation causes nondisjunction of chromosome 4 centromeres (L. V. Morgan, 1940, DIS 13: 51). # T(1;4)N264: Translocation (1;4) Notch origin: X ray induced. discoverer: Demerec. translocation cytology genetics ____________________________________________________________________________ T(1;4)N264-12 (| 3C6-7;101F (Sutton) mutant for N; variegates for w, rst; ci+ shows weakened dominance *T(1;4)N264-20 / 3C4-5;3C7-8;101F deleted for N; variegates for [3C5-7 missing (Sutton)] w, rst; ci+ shows weakened dominance *T(1;4)N264-113 ` 3C10-D1;101 (102 variegates for w, N; missing) carries normal ci allele (Stern) ( Synonym: T(1;4)Na8. | References: Demerec, 1941, Proc. Int. Congr. Genet., 7th, pp. 99-103; Judd, 1955, DIS 29: 126-27. / New order: 1 - 3C4|101F; 20 - 3C8|101F - 102. ` 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). Not clear that a reciprocal translocation between X and short arm of 4 was adequately ruled out. # T(1;4)Na8: see T(1;4)N264-12 # T(1;4)NO: Translocation (1;4) Nucleolus Organizer cytology: T(1;4)20F;101-102. references: Atwood, 1969, Genetics 61: 319-27. Komma and Endow, 1986, Genetics 114: 859-74. genetics: NO translocated to 4. other information: Useful as source of rDNA in bb- stocks. # T(1;4)pn2a: Translocation (1;4) prune cytology: T(1;4)2D5-6;101F. origin: X ray induced. references: Ilyina, Sorokin, Belyaeva, and Zhimulev, 1980, DIS 55: 205. Slobodyanyuk and Serov, 1983, Mol. Gen. Genet. 191: 372-77. genetics: Mutant for pn. Male lethal. # T(1;4)RF43 cytology: T(1;4)3A2-3;101-102 (complex). origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. Allele of l(1)3Ac. #*T(1;4)RF60 cytology: T(1;4)3C;101-102. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. N allele. #*T(1;4)sc10-2: Translocation (1;4) scute cytology: T(1;4)1A;102F + T(1;4)1D;101F; two reciprocal 1-4 translocations, according to Schultz. origin: X ray induced in In(1)ac3. discoverer: Sturtevant, 1930. references: 1934, Proc. Nat. Acad. Sci. USA 20: 515-18. 1936, Genetics 21: 444-66. genetics: Mutant for sc. Virtually male lethal. X chromosome broken between M(1)1B 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. 4PXD carries X-chromosome loci from y through M(1)1B and was used extensively by Sturtevant (1934, 1936) in his studies on preferential segregation. The XP4D element survives in the heterozygous female but is an extreme Minute owing to defi- ciency for M(1)1B and is rarely fertile. # T(1;4)scH: Translocation (1;4) scute of Hackett cytology: T(1;4)1B4-C3;101-102; inferred from genetic results. origin: / ray induced. discoverer: Hackett, 46a. references: Muller and Valencia, 1947, DIS 21: 70. Garcia-Bellido, 1979, Genetics 91: 491-520. genetics: Relatively viable and sc (Garcia-Bellido, 1979). Two halves of the translocation may be recovered separately. XP4D is deficient for y and sc but not M(1)1B and carries ey+. 4PXD covers Df(1)sc19 and therefore carries a normal allele of l(1)sc. T(1;4)scH/ci is ci+. molecular biology: X-chromosome breakpoint between coordinates +5.9 and +6.4 (Carramolino, Ru'z-G'mez, Guerrero, Campuzano, and Modolell, 1982, EMBO J. 10: 1185-91). # T(1;4)Sidky cytology: T(1;4)13C;101-102. references: McKee, 1987, Genetics 116: 409-13. # T(1;4)V46 cytology: T(1;4)7D10-11;101F-102A. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. genetics: Recessive lethal associated with 4. #*T(1;4)w13: see Tp(1;4)A1 # T(1;4)w70L26.5: Translocation (1;4) white cytology: T(1;4)3C1-2;12B8-9;102F. Ring-like chromomere com- plex in 3C1; remnants of band material between 3C1 and 3C2 missing (Sorsa, 1973). new order: 1 - 3C1|102F - 101; 102F|12B8 - 3C2|12B9 - 20. origin: X ray induced in In(1)z+64b9 = In(1)3C1-2;12B8-9. references: Sorsa, 1973, Cold Spring Harbor Symp. Quant. Biol. 38: 601-08. Sorsa, Green, and Beermann, 1973, Nature (London) New Biol. 245: 34-37. genetics: Homo- and hemizygous viable with white eyes. #*T(1;4)w258-43 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)wm3: see T(1;4)A3 # T(1;4)wm5: Translocation (1;4) white-mottled cytology: T(1;4)3C2;101F1-2 (Pipkin and Chakrabartty, 1975, Genetics 80: s64). Duplication 1.9 times the length of 4 at metaphase. origin: X ray induced. discoverer: Muller, 1929. synonym: T(1;4)m5: Translocation (1;4) mottled-5; T(1;4)A5. references: 1930, J. Genet. 22: 299-334. Bolen, 1931, Am. Nat. 65: 417-22. Grell and Day, 1970, Chromosoma 31: 434. 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. 4PXD added to a normal male genome produces males with 20% normal viability that are weakly fertile; added to a diploid female genome, it produces a fertile hyperploid genome; and added to a triploid intersex genome, it is virtu- ally lethal. XP4D 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 deriva- tives of T(1;4)wm5. #*T(1;4)wm11 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)wm11. # T(1;4)wm258-18 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 4PXD element survives as a duplication. # T(1;4)wm258-21 cytology: T(1;4)3E5-6;101F (Demerec and Hoover). origin: X ray induced. discoverer: Demerec, 1934. synonym: T(1;4)wvD3: Translocation (1;4) white-variegated of Demerec. references: Hartmann-Goldstein, 1967, Genet. Res. 10: 143-59. Cowell and Hartmann-Goldstein, 1980, Chromosoma 79: 329-40. Kornher and Kauffman, 1986, Chromosoma 94: 205-16. genetics: Variegates for w, fa, spl, N, Sgs-4, dm, and M(1)3E but not ec or bi. Also variegates for ci (Gersh). Low tem- perature increases variegation of larval Malpighian tubules and also heterochromatic appearance of the transposed euchromatin (Hartmann-Goldstein, 1967). Cytological compac- tion of the Sgs-4 locus (3C11-12) enhanced at low temperature (17C) and Sgs-4 protein and transcript reduced in transloca- tion heterozygotes at this temperature (Kornher and Kauffman, 1986). Males usually lethal; survivors probably X/Y/Y. Cell lethal in X/0 tissue in gynandromorphs (Judd, 1953, DIS 27: 95). #*T(1;4)wm258-31 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)wm258-53 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)wmA: 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)wmD3: 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)wmDV4: 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 indi- cate 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 4PXD element of T(1;4)wmDV4 survives as a duplica- tion and carries wmDV4, the left break in the X chromosome is between w and N. # T(1;4)wmJ: Translocation (1;4) white-mottled of Jonsson cytology: T(1;4)3C2-3;20F;102C. new order: 1 - 3C2|20F - 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 XP4D element of the translocation has become separated from the 4PXD element and lost. The 4PXD 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 hetero- chromatin is virtually random disjunction of X and Y chromo- somes. 4PXD 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 hetero- chromatin. # T(1;4)wmK: Translocation (1;4) white-mottled of Krist cytology: Distal tip of X translocated to centromere of 4. origin: X ray induced. references: Breugel, 1972, Genetica 43: 25-42. genetics: Variegates for w. Most of the homozygous females and hemizygous males have mottled eyes with large spots; a few have almost wild-type or pale eyes without large spots. More pigment at 25 than at 16. #*T(1;4)wmMed: Translocation (1;4) white-mottled of Medvedev discoverer: Medvedev, 1934. genetics: Variegated for w and probably rst. Arose in wa and therefore has light eye color. # T(1;4)wvD3: see T(1;4)wm258-21 # T(1;4)yA74c40 cytology: T(1;4)1B1-2;101F. origin: Induced with caffeine and / rays. references: Alexandrov, Ankina, and Alexandrova, 1985, DIS 61: 212-13. genetics: Mutant for y. # T(1;4)z20G1: 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 4PXD element is poorly viable when added to male genome but viable and fertile in female; dupli- cated for w but does not cover lethality of Df(1)wm4Lrst3R = Df(1)3C1-2;3C3-4 (Gersh, 1963). # T(1;4)z+ origin: X-ray-induced rearrangements of z-bearing X chromosomes that interfere with z-w+ interaction. genetics: z+ phenotype. references: Gelbart, 1971, Ph.D. Thesis, Univ. of Wisconsin. translocation cytology ____________________________ T(1;4)z+12 3C6-7;101A T(1;4)z+31 3C3-5;101B-C T(1;4)z+34 3C2-3;102F T(1;4)z+54 3C;3F;102D-E # T(1;A)A7 cytology: T(1;A)2D;?. Autosomal break in heterochromatin. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. # T(1;A)GF332 cytology: T(1;A)3E5;?. Autosomal break in heterochromatin. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. #*T(1;A)pn-ec: see Tp(1;2)w+62g # T(1;A)RF52 cytology: X break in 3E; autosomes complex. origin: X ray induced. discoverer: Lefevre. genetics: Male lethal. # T(X.2)Inx and 3: see *T(1;2)wm53e # T(Xc2;2)26: see Tp(1;2)26