# T(2;?)odd5.1: see Tp(2;?)5.1 # T(2;3)3.29 cytology: T(2;3)25C;100F. origin: X ray induced. discoverer: Nusslein-Volhard. synonym: T(2;3)odd3.29. references: Nusslein-Volhard, Kluding, and Jurgens, 1985, Cold Spring Harbor Symp. Quant. Biol. 50: 145-54. genetics: Second chromosome breakpoint between slp and mid; neither gene mutant. # T(2;3)63 origin: / ray induced. discoverer: Hinton, 63b. references: 1964, DIS 39: 61 (except for T(2;3)63-5). 1965, Genetics 51: 971-82. translocation cytology genetics ____________________________________________________________________________ T(2;3)63-1 49D-E;79B-C homozygous viable, fertile; eyes slightly rough T(2;3)63-2 27B-C;75C homozygous lethal T(2;3)63-3 ( 40-41;80-81 homozygous lethal T(2;3)63-5 40C;89E-F + In(3L)69-70;79-80 T(2;3)63-6 59E-F;89E-F homozygous viable, fertile; short bristles; wings obliquely creased, ovate, often asymmetrical T(2;3)63-7 41C;92D-E homozygous lethal T(2;3)63-8 36E;86B homozygous lethal T(2;3)63-9 34A-B;75C homozygous lethal *T(2;3)63-10 33-34;76D-E homozygous viable but sterile; abdominal tergites more pigmented than in wild type T(2;3)63-13 24-25;94D-E homozygous viable, fertile; variegated eye color T(2;3)63-14 38A-B;69A-B homozygous lethal T(2;3)63-15 41D;64A homozygous lethal; variegated eye color in heterozygote T(2;3)63-16 41C-D;93A-B homozygous viable, fertile; eyes slightly rough T(2;3)63-17 40C;96A-B homozygous lethal; eye color in heterozygote variegated over SM5 but normal over bw or + T(2;3)63-18 39B-C;80C homozygous viable, fertile; trough-like wing posture in 90% of flies T(2;3)63-19 24D-E;80C homozygous lethal T(2;3)63-21 32E;89C-E + In(3LR)65B;84B T(2;3)63-22 40B;84D homozygous lethal T(2;3)63-23 ( 40-41;80-81 homozygous lethal ( Inferred from genetic data because salivary chromosomes appear normal. # T(2;3)64 origin: / ray induced. discoverer: Hinton, 63b. references: 1965, Genetics 5l: 971-82. translocation cytology _____________________________________________ T(2;3)64-31 36D-E;96B-C + In(2R)41E-F;55F T(2;3)64-32 35D-E;70C-D T(2;3)64-33 ( 40-41;80-81 T(2;3)64-34 25D;86C T(2;3)64-35 40B;92C T(2;3)64-36 40D;85E T(2;3)64-37 60E;82F ( Inferred from genetic data because salivary chromosomes appear normal. #*T(2;3)100r20: see T(1;2;3)100r20 # T(2;3)101 cytology: T(2;3)44B;83E-F (Lewis, 1956, DIS 30: 130). discoverer: Sturtevant. genetics: Homozygous viable; male fertile and female sterile. Crossing over about normal in chromosome 2 of heterozygous female. #*T(2;3)103 discoverer: Sturtevant. genetics: Homozygous lethal. Reciprocal translocation with breaks in 2L and 3L. Crossing over in heterozygous female low in 2L, normal in 2R. # T(2;3)108 cytology: T(2;3)37-38;52D-F;80;81 + T(2;3)42A2-3;58A4-B1 inferred from a combination of cytological [52D-F (Lewis, 1951, DIS 25: 108-9)] and genetic observations. new order: 21 - 37|(80 - 81)|52D - 42A3|58B1 - 60; 61 - 80|(37 - 42A2|58A4 - 52F)|81 - 100. origin: Arose in In(2R)Cy = In(2R)42A2-3;58A4-B1. discoverer: Sturtevant. references: Bahn, 1971, Hereditas 67: 75-78. genetics: Mutant for Rev. Homozygous semilethal. The segre- gant that receives a normal chromosome 2 and the transposed element that might be designated 3LD2LP3RD survives and is fertile. It is duplicated for the loci of pr, lt, rl, tk, and according to Lewis, for M(2)53, sm, and hy; not deficient for chromosome 3 genes. # T(2;3)109 cytology: T(2;3)22F-23B;55F-56A;80 (Lewis, 1951, DIS 25: 108- 9). new order: 21 - 22F|55F - 23B|80 - 61; 60 - 56A|80 - 100. discoverer: Sturtevant. genetics: Homozygous viable and wild type. Originated in In(3R)P but is separable from it. #*T(2;3)110 origin: X ray induced. discoverer: Sturtevant. genetics: Homozygous lethal. Wings short, extended, and coiled downward in spiral. L4 and marginal veins thickened, L4 some- times not reaching margin; posterior wing cell reduced. Pos- terior crossvein absent; L5 reduced and irregularly plexate. Break in 2R near vg and one in 3R, which carries In(3R)P. New order is 2L + 3L and 2R + 3R. #*T(2;3)135 cytology: T(2;3)37;85A. origin: X ray induced simultaneously with T(1;2)l-v135. references: Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1663. # T(2;3)203 cytology: T(2;3)57A5-10;84C8-D1 interband (B.S. Baker, 1985). discoverer: Ou. genetics: Transvects Cbx Ubx/+. # T(2;3)205 cytology: T(2;3)41;89D (E.B. Lewis). origin: X ray induced in Canton-S. discoverer: Ou. # T(2;3)221 cytology: T(2;3)22B;62F (E.B. Lewis). origin: X ray induced in Canton-S. discoverer: Ou. references: Craymer, 1984, DIS 60: 234-36. genetics: Discovered in association with In(3R)221; does not transvect Cbx Ubx/+. # T(2;3)429 - T(2;3)445 origin: X ray induced. discoverer: Gelbart. translocation cytology _________________________________________________________ T(2;3)429.3 23A1-2;83C1-2 T(2;3)429.9 38D-E;85C + Df(2L)22D5-6;23B1-2 T(2;3)429.25 40;61F T(2;3)429.33 40;65E + Tp(3;2)70C;71B T(2;3)429.80 22F3-23A1;31C;35C;70A;81A;92C T(2;3)432.4 23C;41A;70B3-C1 T(2;3)432.12 23D;70D T(2;3)432.30 26C;71E-F;81F T(2;3)432.45 23D1-2;80F T(2;3)434.5 25A1-2;81F T(2;3)434.9 24A1-2;80F T(2;3)434.12 21F3-4;84F13-14 (B.S. Baker) + 49E-F;90C T(2;3)434.17 22C;25A1-2;55A1-2;85A1-2;98F T(2;3)434.19 22C;40;68E;80F;81F;96D T(2;3)434.25 28E-F;81F(?) T(2;3)434.31 see T(2;3)DTD36 T(2;3)434.32 49E-F;97A-B T(2;3)434.35 36C;64D-F + 44E;78E T(2;3)434.37 40;68B-D + In(2LR)21E;59C T(2;3)434.54 21B;90A1-2 T(2;3)434.60 57E-F;84A-B + In(2LR)34D;41A T(2;3)434.61 31E-F;90C-D T(2;3)434.64 21F-22A1;27E;75C T(2;3)434.71 see T(2;3)DTD46 T(2;3)434.74 22F3-23A1;78A1-2 T(2;3)434.102 21F;34A1-2;41A;51F;96C T(2;3)434.121 22B;32B;42A;43A;74E-F; 81F;85A T(2;3)434.122 24F;76D;81F;89E1-3 T(2;3)434.125 35F;84E9 (B.S. Baker) + In(2LR)22A;41A-C T(2;3)434.128 24A1-2;68F1-2 T(2;3)434.131 25D3-4;97A2-4 T(2;3)434.32 49E-F;97A-B T(2;3)434.9 24A1-2;80F T(2;3)445.1-2 41A;98A10-15 T(2;3)445.2-1 27C3-8;82D T(2;3)445.2-2 33D;82F T(2;3)445.2-3 40-41;80-81(?) T(2;3)445.2-4 52F;67E4-F1 T(2;3)445.2-5 40B;69A4-B1 T(2;3)445.2-7 35E;89A;92A T(2;3)445.2-9 40-41;80-81(?) T(2;3)445.2-10 58C3-D1;93F T(2;3)445.3-1 57B;77B T(2;3)445.3-2 42A16-19;86E6-F1 T(2;3)445.3-3 21C1-2;67F T(2;3)445.3-4 40;95B # T(2;3)A cytology: T(2;3)39B-C;83B (Lewis, 1951, DIS 25: 108-9). origin: X ray induced in Bl. discoverer: Dobzhansky, 28h. references: 1929, Biol. Zentr. 49: 408-19. 1933, Z. Indukt. Abstamm. Vererbungsl. 64: 269-309. Dobzhansky and Sturtevant, 1931, Carnegie Inst. Washington Publ. No. 421: 29-59. genetics: Homozygous lethal. #*T(2;3)A1: Translocation (2;3) from Austin origin: X ray induced. references: Patterson, Stone, Bedichek, and Suche, 1934, Am. Nat. 68: 359-69. Pipkin, 1940, Texas Univ. Publ. 4032: 73-125. genetics: Homozygous viable and fertile. Chromosomes 2 and 3 broken at chromocenter. 2L attached to 3R and 3L to 2R. # T(2;3)A1-W: Translocation (2;3) A1 of Wallace cytology: T(2;3)22;68 superimposed on In(2L)22D1-2;33F5-34A1 + In(2R)42A2-3;58A4-B1 + In(3LR)61A-C;74;89D-E;93B;96A. origin: Spontaneous in In(2L)Cy In(2R)Cy; TM2. references: Wallace, Zouros, and Krimbas, 1966, Amer. Nat. 100: 245-51. Wallace, 1966, Amer. Nat. 100: 565-83. Thompson, 1977, Genetics 85: 125-40. 1983, DIS 59: 129-30. genetics: Homozygous lethal because of the dominant markers in the component balancers In(2L)Cy In(2R)Cy, Cy L and In(3LR)Ubx130, Ubx130 es (TM2). Segregates as a unit and suppresses recombination in chromosomes 2 and 3. # T(2;3)A2 cytology: T(2;3)46B;47F;78A. new order: 21 - 46B|47F - 46B|78A - 61; 60 - 47F|78A - 100. origin: X ray induced. references: Ashburner, 1972, DIS 49: 34. genetics: Homozygous lethal. #*T(2;3)A26 origin: X ray induced. discoverer: Muller. references: Painter and Muller, 1929, J. Heredity 20: 287-98. Muller, 1930, J. Genet. 22: 299-334. genetics: Break in 3R between sr and e. # T(2;3)A147: see T(Y;2;3)A147 # T(2;3)abd-A: Translocation (2;3) abdominal-A origin: X ray induced. genetics: Mutant for abd-A. molecular translocation cytology discoverer ref ( biology | ________________________________________________________________________ T(2;3)abd-A517 / 34-5;41;78;83-84;89E Baker 40-45 kb T(2;3)abd-AMX1 40;89E1-2 Morata 1, 2 54-56 kb T(2;3)abd-AS2 37C;69D;89E;complex Tiong 1, 3 50-55 kb ( 1 = Karch, Weiffenbach, Peifer, Bender, Duncan, Celniker, Crosby, and Lewis, 1985, Cell 43: 81-96; 2 = Sanchez-Herrero, Vernos, Marco, and Morata, 1985, Nature 313: 108-13; 3 = Tiong, Bone, and Whittle, 1985, Mol. Gen. Genet. 200: 335-42. | Coordinates of 89E breakpoints in kilobases to the right of the right breakpoint of In(3R)Cbxrv1. / Synonym: iab231616.517. # T(2;3)Adh1: Translocation (2;3) Alcohol dehydrogenase cytology: T(2;3)33E9-34A1;89A3-7 (Ashburner); originally described as T(2;3)35A;35D;89A (Nash, 1970). origin: X ray induced as a "double-crossover" in a b+ rkEMS el+ AdhD/b rk+ el AdhF female. discoverer: E.H. Grell. synonym: T(2;3)DpAdh1. references: Grell, 1969, Genetics 61: s23. Nash, 1970, Genetics 64: 471-99. Ashburner, 1982, Genetics 101: 447-59. genetics: Originally described as duplicated for Adh (Nash, 1970), but presumably has undergone spontaneous exchange and no longer carries the Adh duplication nor enhances H (Ash- burner). # T(2;3)AntpCtx: Translocation (2;3) Antennapedia-Cephalothorax cytology: T(2;3)35B;84B1-2 + In(2R) (Ashburner). origin: X ray induced. discoverer: Duncan and E.B. Lewis. synonym: T(2;3)Ctx. references: Scott, Weiner, Hazelrigg, Polisky, Pirrotta, Scalenghe, and Kaufman, 1983, Cell 35: 763-76. Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95. genetics: Recessive lethal. Heterozygotes show transformation of dorsal head structures into dorsal thoracic structures and, occasionally, transformation of antennae into legs. molecular biology: Third-chromosome breakpoint 165-166 kb distal to proximal breakpoint of Tp(3;3)Dfdrv16. # T(2;3)Antprk4: Translocation (2;3) Antennapedia-recessive cytology: T(2;3)36C-D;84B1-2 + In(3LR)62B;98F. origin: X ray induced. synonym: T(2;3)antpXbk4. references: Lewis, Kaufman, Denell, and Tallerico, 1980, Genet- ics 95: 367-81. Scott, Weiner, Hazelrigg, Polisky, Pirrotta, Scalenghe, and Kaufman, 1983, Cell 35: 763-76. Abbott and Kaufman, 1986, Genetics 114: 919-42. genetics: Recessive lethal without dominant phenotype. molecular biology: Third-chromosome breakpoint 120 kb distal to the proximal breakpoint of Tp(3;3)Dfdrv16. # T(2;3)AntprL1 cytology: T(2;3)25F;84B2. origin: X ray induced. synonym: T(2;3)antpL1. references: Abbott and Kaufman, 1986, Genetics 114: 919-42. genetics: Recessive lethal without dominant phenotype. # T(2;3)Antprv genetics: Revertant of Antp. Homozygous lethal. translocation cytology origin ( synonym ref | ____________________________________________________________________________ T(2;3)Antprv5 60B3;84B1-2;97B3 2 T(2;3)Antp73b-RX5 2 T(2;3)Antprv6 57B6-8;84B1-2 2 T(2;3)Antp73b+RX6 2 T(2;3)Antprv7 40;84B1-2 2 T(2;3)Antp73b+RX7 2 T(2;3)Antprv8 / 41;84B1-2 1 T(2;3)AntpNs+RC8 4, 5 T(2;3)Antprv13 ` 40-41;84A4-B2 3 T(2;3)AntpNs+R13 1, 3 ( 1 = EMS induced (Struhl, 1981); 2 = X ray induced in In(3R)Antp73b = In(3R)84B1-2;84C5-6; 3 = X ray induced in AntpNs. | 1 = Duncan and Kaufman, 1975, Genetics 80: 733-52; 2 = Hazel- rigg and Kaufman, 1983, Genetics 105: 581-600; 3 = Lewis, Kaufman, Denell, and Tallerico, 1980, Genetics 95: 367-81; 4 = Scott, Weiner, Hazelrigg, Polisky, Pirrotta, Scalenghe, and Kaufman, 1983, Cell 35: 763-76; 5 = Struhl, 1981, Nature 292: 635-38. / Lethal with AntpB. ` Molecular biology: Third-chromosome breakpoint 144-147 kb distal to the proximal breakpoint of Tp(3;3)Dfdrv16 (Scott et al., 1983). # T(2;3)AntpScx: see T(2;3)Scx # T(2;3)AntpYu: Translocation (2;3) Antennapedia of Yu cytology: T(2;3)22A4-5;84B2-4 + T(2;3)37B1-2;98B1-2 (Kaufman et al., 1980). new order: 21 - 22A4|84B4 - 98B1|37B1 - 22A5|84B2 - 61; 60 - 37B2|98B2 - 100. origin: X ray induced. discoverer: Yu, 1948. references: 1949, Ph.D. Thesis, Calif. Inst. Tech. Lewis, 1956, DIS 30: 76. Kaufman, Lewis, and Wakimoto, 1980, Genetics 94: 115-33. genetics: Mutant for Antp; associated with 84B2-4 breakpoint. Homozygous lethal. # T(2;3)apXa: Translocation (2;3) apterous-Xasta cytology: T(2;3)41F;89E8-F1 superimposed on In(2R)42A2-3;58A4- B1 + In(3R)89C2-3;96A18-19 (Bridges in Morgan, Bridges, and Schultz, 1936, Year Book - Carnegie Inst. Washington 35: 294; correction by Lewis, 1951, DIS 25: 108-9). new order: 21 - 41F|89E8 - 89C3|96A19 - 100; 60 - 58B1|42A3 - 58A4|42A2 - 41F|89F1 - 96A18|89C2 - 61. origin: X ray induced in In(2R)Cy; In(3R)P. discoverer: Serebrovsky, 28a. synonym: T(2;3)Xa: Translocation (2;3) Xasta. references: Serebrovsky and Dubinin, 1930, J. Hered. 21: 259- 65. Sturtevant, 1934, DIS 2: 19. genetics: Dominant mutant for ap. Homozygote virtually lethal. other information: The first X-ray-induced mutation recovered in the USSR. Useful as a balancer of 2R and 3R. #*T(2;3)astrv1: Translocation (2;3) asteroid-reverted cytology: T(2;3)21E2-3;68C2-3;88D8-9. new order: 21A - 21E2|88D8 - 68C3|88D9 - 100; 61 - 68C2|21E3 - 60. origin: X ray induced in al ast ho. discoverer: E.B. Lewis, 1942. references: 1945, Genetics 30: 158. genetics: Associated with a reversion of ast. Homozygous lethal. #*T(2;3)astrv3 cytology: T(2;3)21E2-3;61C2-3. origin: X ray induced in net ast dp cl. discoverer: E.B. Lewis, 1942. references: 1945, Genetics 30: 158. genetics: Associated with reversion of ast. Lethal homozygous and heterozygous with Df(2L)S4 = Df(2L)21C3-4;22B2-3. # T(2;3)AsxT1: Translocation (2;3) Additional sex combs cytology: T(2;3)41-42;84E-F;88B. new order: 21 - 41|88B - 84F|88B - 100; 61 - 84E|42 - 60. origin: / ray induced in Oregon-R. discoverer: Tiong. synonym: T(2;3)OR-6-6-1. genetics: Associated with AsxT1 but should be separable. #*T(2;3)Ata: Translocation (2;3) Arista cytology: T(2;3)40;66F-67A + T(2;3)47;81. new order: 21 - 40|67A - 81|47 - 60; 61 - 66F|40 - 47|81 - 100. origin: X ray induced. discoverer: Krivshenko, 1949. synonym: T(2;3)At (symbol preoccupied). references: 1954, DIS 28: 74-75. 1955, DIS 29: 73. genetics: Associated with Ata. Homozygous lethal. # T(2;3)AWT1 cytology: T(2;3)29F;94B. origin: Spontaneous in AW chromosome line during successive backcross programs. references: Yamaguchi and Mukai, 1974, Genetics 78: 1209-21. # T(2;3)b: Translocation (2;3) black references: Alexandrov and Alexandrova, 1986, DIS 63: 159-61. genetics: Mutant or deficient for b. translocation cytology origin comments ____________________________________________________________________ T(2;3)b79b6 33E10;34D6;79D3;80 T(2;3)b79d6 34A2-3;34D8-E2;79B;80C neutrons homozygous + / rays lethal *T(2;3)b83l2 34B12-C1;35A2-A23;83A3-7;83C neutrons homozygous + Df(2L)34C2;34E4-5 lethal T(2;3)b85c2 34C7-D1;34E1-2;94C4-D1 neutrons viable homozygous sterile # T(2;3)B cytology: T(2;3)33;81F (Lewis, 1951, DIS 25: 108-9; 1954, Am. Nat. 88: 225-38). origin: X ray induced. discoverer: Dobzhansky, 28h. references: 1929, Biol. Zentr. 49: 408-19. Dobzhansky and Sturtevant, 1931, Carnegie Inst. Washington Publ. No. 421: 29-59. genetics: Homozygous lethal. Crossing over reduced in 2L. # T(2;3)Ba15 cytology: T(2;3)60E5-6;64B12-C12. synonym: DllJ;BaJ. references: Cohen, Bronner, Kuttner, Jurgens, and Jackle, 1989, Nature, 338: 432-34. genetics: Mutant for Ba. molecular biology: 60E breakpoint located on molecular map (Cohen et al., 1989). # T(2;3)BTD: Translocation (2;3) Bithorax Transvection Disrupter origin: / ray induced. references: Smolik-Utlaut and Gelbart, 1987, Genetics 116: 285-98. translocation cytology _____________________________________ T(2;3)BTD3 40;87F + In(3R)81;85D T(2;3)BTD5 25C;64C;89C T(2;3)BTD6 27E;81 T(2;3)BTD10 50C;81 # T(2;3)BTD73 cytology: T(2;3)58A1;81F. references: Schejter and Shilo, 1989, Cell 56: 1093-1104. # T(2;3)bwD Translocation (2;3) brown-Dominant origin: / ray induced. references: P. Simpson. translocation cytology __________________________________ T(2;3)BTDDrv12 59D4-E1;66D1 T(2;3)BTDDrv18 59D4-D10;98F13-14 # T(2;3)bwR: Translocation (2;3) brown-Rearranged origin: X ray induced. discoverer: Slatis. references: 1955, Genetics 40: 5-23. genetics: Associated with corresponding bwR. translocation cytology ____________________________ *T(2;3)bwR4 59E2-3;80-81 *T(2;3)bwR12 59D;80C *T(2;3)bwR14 59E2-3;80 *T(2;3)bwR15 59D;80C # T(2;3)bwV: Translocation (2;3) brown-Variegated origin: X ray induced. genetics: Variegated for bw. translocation cytology discoverer ( ref | _________________________________________________________________ *T(2;3)bwV3 / 2R break near bw; 3 1, 2 3L break just left of centromere T(2;3)bwV4 / 2R break near bw; 4 1, 2, 3 3L break near centromere T(2;3)bwV5 / 2R break near bw; 4 1, 2 3L break near centromere *T(2;3)bwV6 ` probably breaks in 2L, 2 1, 2 2R, and 3R *T(2;3)bwV8 2R break at bw; 1 3R break near p ( 1 = Levy, 1932; 2 = Moore, 1929; 3 = Muller; 4 = Patterson. | 1 = Glass, 1933, J. Genet. 28: 69-112; 2 = Glass, 1934, Am. Nat. 68: 107-14; 3 = McKee, 1984, Genetics 106: 403-22. / Translocation parts interchangeable in T(2;3)bwV3, T(2;3)bwV4, T(2;3)bwV5 without altering phenotype. ` Crossing over reduced in 2L, 2R, and base of 3R; eye color reverted to wild type but translocation remained. #*T(2;3)bwV30k12 origin: X ray induced. discoverer: Van Atta, 30k12. references: 1932, Genetics 17: 637-59. genetics: Variegated for bw. Complex rearrangement with breaks in 2L near centromere, 2R near bw, and 3L near centromere; appears to carry an inversion in 3R. #*T(2;3)bwV30k13 origin: X ray induced. discoverer: Van Atta, 30k13. references: 1932, Genetics 17: 637-59. genetics: Variegated for bw. Breaks in 2R near c and bw and in 3R near cu. #*T(2;3)bwVD: Translocation (2;3) brown- Variegated Dichaete linked origin: X ray induced. discoverer: Oliver, 29k24. references: 1932, Z. Indukt. Abstamm. Vererbungsl. 61: 447- 88. genetics: Variegated for bw. Homozygous lethal. # T(2;3)bwVDe3: Translocation (2;3) brown- Variegated of Demerec cytology: T(2;3)59D;81F. Also an inversion in 2R. origin: X ray induced. discoverer: Demerec, 33j14. genetics: Variegates for bw and mi but not abb. Mutant for Dfd. Homozygous lethal. Gives transvection effects with cer- tain pairs of bithorax pseudoalleles (Lewis, 1955, Am. Nat. 89: 73-89). # T(2;3)bwVDe4 cytology: T(2;3)59D2-4;80 (Schultz). origin: X ray induced. discoverer: Demerec, 33k22. genetics: Variegates for bw and mi. Homozygous lethal. # T(2;3)bxd: Translocation (2;3) bithoraxoid origin: X ray induced. genetics: Mutant for bxd. translocation cytology discoverer _____________________________________________________ T(2;3)bxd68 41;89E Baker T(2;3)bxd123 41;89E Crosby T(2;3)bxd127 59C;89E + E.B. Lewis In(3R)88C-D;92 T(2;3)bxd266 40;89E Tung T(2;3)bxdDB1 41;89E D. Baker T(2;3)bxdDB3 48;89E D. Baker T(2;3)bxdDB4 32;89E D. Baker T(2;3)bxdDB5 41;89E D. Baker T(2;3)bxdDB6 22A;43A-C;80D;84;89E;92F D. Baker T(2;3)bxdX 42B-C;89E1-2 E.B. Lewis # T(2;3)C origin: X ray induced. discoverer: Dobzhansky, 28h. references: 1929, Biol. Zentr. 49: 408-19. Dobzhansky and Sturtevant, 1931, Carnegie Inst. Washington Publ. No. 421: 29-59. genetics: Break near centromere in chromosomes 2 and 3. New order is 2L + 3L; 2R + 3R. Homozygous lethal. # T(2;3)C4 - T(2;3)C591: Translocation (2;3) Crossover suppressor origin: X ray induced; selected on the basis of reduced recom- bination in heterozygous females. references: Thomas and Roberts, 1966, Genetics 53: 855-62. Roberts, 1970, Genetics 65: 429-48. new homozygous Xover translocation cytology order ( viable? reduced in ___________________________________________________________________________ T(2;3)C4 40-41;94A - 3R T(2;3)C11 40-41;64D;77A 1 + 3L T(2;3)C17 56F;67E - 2R, 3L T(2;3)C24 53B;80-81 + 2R T(2;3)C29 43F;92D + 3R T(2;3)C49 22C-D;86E + 2L T(2;3)C58 40-41;96F - 3R T(2;3)C65 | 40-41;75A;80-81 2 - 3L + In(3L)64C;77A T(2;3)C101 29B;80-81 _ 2L T(2;3)C111 40-41;70F + - 3L In(3L)62B;79D-E T(2;3)C122 60B;80-81 + 2R T(2;3)C124 34D;75F - 2L T(2;3)C132 55E;80-81 - 2R T(2;3)C149 52A;93B - 2R, 3R T(2;3)C157 41;96D-E + + 2L, 3R In(2LR)24F;54F T(2;3)C164 32F;64B - 2L, 3L T(2;3)C177 40-41;62F + - 2R, 3L 56F;79B T(2;3)C199 41;93E - 3R T(2;3)C202 56D;89D + 2R T(2;3)C211 40-41;70C - 3L T(2;3)C218 40-41;70F + 3L T(2;3)C230 35D;61A - 3L T(2;3)C231 50D;62B + - 2R, 3L In(2LR)35C-D;52A-B T(2;3)C248 52C;94D;96B 3 - 2R, 3R T(2;3)C257 50F;80 - 2R T(2;3)C267 21D;63F;64E + - 3L In(3LR)74F;88D T(2;3)C287 56D;89F (Craymer, 1984, - 2R Genetics 108: 573-87) T(2;3)C293 43A;67A;80-81 4 - 3L T(2;3)C304 48A;83C;100B 5 - 3R T(2;3)C308 / 40-41;84B;94D;99B 6 - 3R T(2;3)C309 58D;68F - 2R, 3L T(2;3)C311 54C;64C - 2R, 3L T(2;3)C313 27B;80-81 - 2L T(2;3)C316 25F;80-81 - 2L T(2;3)C317 24D;97D - 2L, 3R T(2;3)C356 29F;80-81 + 2L T(2;3)C591 28D;69D - 2L ( 1 = 21 - 40|77A - 64D|77A - 100; 60 - 40|64D - 61. 2 = 21 - 40|80 - 100; 60 - 40|75A - 64C|77A - 80|75A - 77A|64C - 61 (tentative). 3 = 60 - 52C|94D - 61; 21 - 52C|96B - 94D|96B - 100. 4 = 21 - 43A|67A - 61; 60 - 43A|80 - 67A|81 - 100. 5 = 21 - 48A|100B - 100F; 60 - 48A|83C - 100B|83C - 61. 6 = 21 - 40|94D - 84D|94D - 99B|84B - 61; 60 - 40|99B - 100. | Involvement of chromosome 2 inferred from genetic data. / Variegates for ca but not for Acph-1 (Morrison and MacIntyre, 1978, Genetics 83: 487-97). #*T(2;3)C-K: Translocation (2;3) Curved of Krivshenko cytology: T(2;3)52;76;81;86. new order: 21 - 52|86 - 100; 60 - 52|81 - 76|81 - 86|76 - 61. origin: X ray induced. discoverer: Krivshenko, 55l3. references: 1956, DIS 30: 74. genetics: Associated with C-K. Homozygous lethal. # T(2;3)cand3 Translocation (2;3) claret cytology: T(2;3)44A-B;100B. origin: / ray induced. references: Sequeira, Nelson, and Szauter, 1989, Genetics 123: 511-214. genetics: Distal break near but distinct from Cand3. # T(2;3)cav cytology: Df(3R)81F;99C-E + T(2;3)59D;94. new order: 21 - 59D|94 - 99C|81F - 94|59D - 60; 61 - 81F|99E - 100. references: Craymer, 1980, DIS 55: 199. genetics: Associated with variegation for ca. Possible to recover the T(2;3) without the deficiency as a consequence of double crossover. The reciprocal product not recoverable; the deficiency is too large. # T(2;3)CA: Translocation (2;3) CAmbridge discov. or translocation cytology origin ref ( associated with ________________________________________________________________________ T(2;3)CA1 45D1-2;96D10-11 X ray 2 Df(2L)A63 T(2;3)CA2 42D6;67A3-4 X ray 2 Df(2L)A63 T(2;3)CA3 41F;90A-B X ray 2 Df(2L)A178 T(2;3)CA7 22B4-5;100B5 / ray 1 Df(2L)osp141 T(2;3)CA8 36B8;67F1-2 / ray 1 Df(2L)osp141 T(2;3)CA9 25A3-8;67C3 / ray 3 Df(2L)TE35A-3 T(2;3)CA15 42F;100F / ray 1 In(3L)fz4 T(2;3)CA34 21A4;64E3-13 / ray 1 T(2;3)CA43 57C;64E-F / ray 1 T(2;3)CA46 54C;64A / ray 1 Df(2L)TE35A-8 T(2;3)CA47 50A-B;84A-B / ray 1 In(2LR)TE35A-205 T(2;3)CA48 45E-F;75C / ray 1 In(2LR)TE35A-205 T(2;3)CA54 50B;81 / ray 1 T(2;3)GT8 T(2;3)CA56 40;70D / ray 1 T(2;3)CA57 43A3;43F6 / ray 1 ( 1 = Ashburner; 2 = Ashburner, Aaron, and Tsubota, 1982, Genet- ics 102: 421-35; 3 = Velissariou. # T(2;3)cb25-17 origin: / ray induced. discoverer: Lyttle. cytology: T(2;3)52B;99C. # T(2;3)Ctx: see T(2;3)AntpCtx # T(2;3)CyrvC3: Translocation (2;3) Curly-revertant cytology: T(2;3)23B3-8;72F3-4 + In(2L)22D1-2;33F5-34A1. new order: 21 - 22B3|72F4 - 100; 61 - 72F3|22B8 - 22D1-2|33F5 - 22D2|34A1 - 60. origin: X ray induced in In(2L)Cy. discoverer: Littlewood. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. genetics: Revertant of Cy. #*T(2;3)D origin: X ray induced. discoverer: Dobzhansky, 28h. references: 1929, Biol. Zentr. 49: 408-19. Dobzhansky and Sturtevant, 1931, Carnegie Inst. Washington Publ. No. 421: 29-59. genetics: Heterozygote short lived and frequently sterile, especially in female. Wings misshapen and legs short. # T(2;3)D4: Translocation (2;3) with Dichaete-4 cytology: T(2;3)21D;70-71 (Lewis). origin: X ray induced. discoverer: Sigmund, 1978. references: Craymer, 1980, DIS 55: 197-200. genetics: Mutant for D (missing alulae) and deficient for ds (shortened wings with close crossveins and widely spaced pos- terior scutellar bristles); also body small. Homozygous lethal and lethal over D; T(2;3)D4/dsW shows mutant charac- teristics of dsW/dsW. # T(2;3)dp5 cytology: T(2;3)25A2-3;95B3-5. 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 dp. # T(2;3)dp6 cytology: T(2;3)25A2-3;81F. 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: Mutant for dp. # T(2;3)dpD: Translocation (2;3) dumpy-Dominant cytology: T(2;3)25A;95B-D (Lewis). origin: X ray induced. discoverer: E.B. Lewis, 1962. references: Del Campo, 1963, DIS 38: 32. genetics: Mutant for dp. Homozygous lethal. # T(2;3)dpw1: Translocation (2;3) dumpy-warped origin: X ray induced. discoverer: Schalet, 1955. references: Carlson and Schalet, 1955, DIS 29: 71-72. Carlson, 1958, DIS 32: 117-18. genetics: Apparently variegated for dp. Homozygous lethal. # T(2;3)Dp-S: Translocation (2;3) with Duplication Star cytology: T(2;3)21D4-E1;81F superimposed on Dp(2;2)21D2- 3;21E2-3. new order: 21A - 21E2|21D3 - 21D4|81F - 61; 60 - 21E1|81F - 100. origin: X ray induced in Dp(2;2)S, ast ast. discoverer: E.B. Lewis. references: 1945, Genetics 30: 137-66. genetics: Y-suppressible expression of ast. # T(2;3)DpAdh1: see T(2;3)Adh1 # T(2;3)dpp: Translocation (2;3) decapentaplegic (W.M. Gelbart) references: Spencer, Hoffmann, and Gelbart, 1982, Cell 28: 451-61. Segal and Gelbart, 1985, Genetics 109: 119-43. Irish and Gelbart, 1987, Genes Dev. 1: 868-79. St. Johnston, Hoffmann, Blackman, Segal, Grimaila, Padgett, Irick, and Gelbart, 1990, Genes Dev. 4: 1114-27. alleles: allele class origin cytology discov ________________________________________________________________________ *T(2;3)dpp3 ( d-III X ray T(2;3)22E3-F1;85B-D Ashburner T(2;3)dpp7 d-III X ray T(2;3)22F1-2;80F Spenser T(2;3)dpp18 d-III X ray In(2L)22F1-2;36C4-6 Spenser + T(2;3)28A1-2;75A1-2 T(2;3)dpp20 d-III X ray T(2;3)22F1-3;64D Spenser T(2;3)dpp22 d-III X ray T(2;3)22F1-3;67E Spenser T(2;3)dpp25 | d-V X ray T(2;3)21F;22F1-3;72A-B;80F Spenser T(2;3)dpp28 d-II EMS T(2;3)22F2-3;86E15-18 Hoffmann T(2;3)dpp29 d-V X ray T(2;3)22F2-3;87D1-2 Gelbart T(2;3)dpp44 d-V / ray T(2;3)22F1-2;80C Irish T(2;3)dpp52 / d-V / ray T(2;3)22F1-2;86A-B Irish T(2;3)dpp71 d-III / ray T(2;3)22F1-2;101 T(2;3)dpp77 d-V / ray T(2;3)22F1-2;80F Segal T(2;3)dpp78 d-V / ray T(2;3)22F1-2;95A1-2 Segal ( Recovered by Faithfull as T(2;3)ho5 + In(2LR)22F1-2;58B (Ash- burner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95). | New order: 21A - 21F|80F - 72B|22F3 - 60; 61A - 72A|21F - 22F1|80F - 100. / Synonym: T(2;3)dppd52 (Irish and Gelbart, 1987, Genes and Development 1: 868-79). # T(2;3)DrL: Translocation (2;3) Drop of Lewis cytology: T(2;3)44;89F-90A + In(3R)89C;95D-96B1. new order: 21 - 44|89F - 89C|96D1 - 100; 60 - 44|90A - 95B1|89C - 61. origin: X ray induced. discoverer: E.B. Lewis. genetics: Mutant for Dr, which is probably independent of rear- rangement. # T(2;3)ds14: Translocation (2;3) dachsous cytology: T(2;3)21D3;50A-B1;87B. new order: 21A - 21D|87B - 61; 60 - 50B1|21D3 - 50A|87B - 100. origin: X ray induced. references: Korochkina and Golubovsky, 1978, DIS 53: 197-200. genetics: Homozygous lethal. Heterozygotes show ds and weak al. # T(2;3)dsx Translocation (2;3) doublesex origin: X ray induced in dsxM. references: Baker, Hoff, Kaufman, Wolfner, and Hazelrigg, 1991, Genetics 127: 125-38. genetics: Recessive dsx. Revertant of dsxM; dsx mutants.. translocation cytology synonym _______________________________________________ T(2;3)dsx30 28F;32F;84A1-2; T(2;3)dsxM+R1 T(2;3)dsx32 84D11-E2;88B1-2 T(2;3)dsxM+R5 59D1-2;84E1-2 T(2;3)dsx45 58A1-2;84E1-2 T(2;3)dsxM+47 # T(2;3)DTD: Translocation (2;3) Disrupter of Transvection at Decapentaplegic origin: X ray induced. 3 and 85-133 induced in Dp(1;2)w+70h, dppho2, 36 and 46 in dpp4 and 85-133 in dppho2 TE23C-D[w+]. genetics: Disrupt transvection at dpp. translocation cytology ref ( _______________________________________________________ T(2;3)DTD3 25F1-2;37B1-2;80 3 T(2;3)DTD14 | 22D-E;70A + 1 31C-D;81F + 35C;92C T(2;3)DTD36 23D1-2;81F 2 T(2;3)DTD43 57E-F;84A-B + In(3LR)35B1-2;41A 2 T(2;3)DTD46 26F;81F 2 T(2;3)DTD66 / 21E;80F + 34D;61A 1 T(2;3)DTD85 34C;78E T(2;3)DTD95 23C;62B T(2;3)DTD97 40A;53F T(2;3)DTD100 24E;60A;81F T(2;3)DTD101 32E-33A;80 T(2;3)DTD102 30B;100D-E T(2;3)DTD104 25C;64A T(2;3)DTD105 22;85B + 39F-40A;95A T(2;3)DTD106 26A;75A + Dp(3;3)81F;82F-83A;95B T(2;3)DTD108 35E-F;81F;82F T(2;3)DTD110 29C;85C + 40C;90C T(2;3)DTD113 24A1-2;68E1-2 T(2;3)DTD115 40;89F-90A T(2;3)DTD118 29E1-2;32B-C;83D T(2;3)DTD120 24E;65F T(2;3)DTD122 32E;89B T(2;3)DTD123 39E-F;89E T(2;3)DTD127 40;88E1-2 T(2;3)DTD130 22E1-2;89A T(2;3)DTD131 26A;46E;100B T(2;3)DTD132 28D;97E T(2;3)DTD133 50A;68A + In(3R)81F;85D ( 1 = Gelbart; 2 = Gelbart, 1982, Proc. Nat. Acad. Sci. USA 79: 2636-40; 3 = Smolnik-Utlaut and Gelbart, 1987, Genetics 116: 285-98. | New order: 21 - 22D|70A - 81F|31C - 22E|70A - 61A; 60F - 35C|92C - 81F|31D - 35C|92C - 100. / New order: 21A - 21E|80F - 61A|34D - 21E|80F - 100; 60 - 34D|61A. # T(2;3)eD8: Translocation (2;3) ebony cytology: T(2;3)40-41;93D1-6. origin: X ray induced. references: D'Alessandro, Ritossa, and Scalenghe, 1977, DIS 52: 46. genetics: Homozygous lethal. Associated with e. # T(2;3)eH1: Translocation (2;3) ebony of Henikoff cytology: T(2;3)40-41;93D. origin: X ray induced. references: Henikoff, 1980, DIS 55: 61-62. genetics: Mutant for e (no variegation even in presence of extra Y). #*T(2;3)E cytology: T(2;3)30B;67E (Schultz). origin: Spontaneous. discoverer: Sturtevant, 1929. references: Dobzhansky and Sturtevant, 1931, Carnegie Inst. Washington Publ. No. 421: 29-59. genetics: Homozygous lethal. # T(2;3)EHH: Translocation (2;3) E of Hilliker and Holm cytology: T(2;3)40;92E-F. new order: 21 - 40F|92E - 61; 60 - 40F|92F - 100; origin: /-ray-induced detachment of C(2L)RM-SH3 C(2R)RM-SH3 females. references: Hilliker and Holm, 1975, Genetics 81: 705-21. genetics: Lethal with Df(2L)C, Df(2L)C', and In(2LR)bwV1; viable with Df(2L)D and Df(2L)D'. Variegates for lt. # T(2;3)E(da): Translocation (2;3) Enhancer of daughterless cytology: T(2;3)41;66C. origin: X ray induced. references: Mange and Sandler, 1973, Genetics 73: 73-86. genetics: Associated with E(da). # T(2;3)E(SD)1: Translocation (2;3) Enhancer of Segregation Distorter cytology: T(2;3)41;100 + Df(2L)E(SD)1 = Df(2L)40A-B;40E. origin: / ray induced. references: Ganetzky, 1977, Genetics 86: 321-55. genetics: Associated with E(SD). # T(2;3)egspy: Translocation (2;3) eagle-spready cytology: T(2;3)33D4-E3;79A4-B1. origin: X ray induced. discoverer: Puro, 1961. synonym: T(2;3)spy. references: 1968, DIS 43: 59. Puro and Arajarvi, 1968, DIS 43: 89-90. 1969, Hereditas 62: 414-18. Puro, 1982, DIS 58: 205-08. genetics: Homozygous viable and fertile. Mutant for eg. # T(2;3)el24: Translocation (2;3) elbow cytology: T(2;3)35B1-3;93C3-7. origin: Induced by ethyl methanesulfonate. genetics: Mutant for el. # T(2;3)en: Translocation (2;3) engrailed genetics: Associated with en. T/T DNA translocation cytology origin ref ( viable? breakpoints | ____________________________________________________________________________ T(2;3)enEs / 48A3-4;84E3-4 X ray 1, 2, 4, + +32 to +33 (B.S. Baker) 5, 6 T(2;3)enLA3 48A;96C EMS 3, 4 + T(2;3)enSF24 48A;90C EMS 2, 3, 4 - +8 T(2;3)enSF37 ` 46C;48A;80 X ray 2, 3, - -31, +5 4, 5 T(2;3)enSF42 48A;65F X ray 2, 4 - -13 T(2;3)enSF50 48A;57A;81A X ray 2, 4 - -3 T(2;3)enSF52 48A;57B;88F X ray 2, 4 - -32 T(2;3)enSF61 48A;89A3;96B X ray 2, 4 - +18 T(2;3)enSF62 48A;84D X ray 2, 4 + -10 ( 1 = Epper and S'nchez, 1983, Dev. Biol. 100: 387-98; 2 = Korn- berg; 3 = Kornberg, 1981, Proc. Nat. Acad. Sci. USA 78: 1095- 99; 4 = Kuner, Nakanishi, Ali, Drees, Gustavson, Theis, Kauvar, Kornberg, and O'Farrell, 1985, Cell 42: 309-16; 5 = Sato, Russell, and Denell, 1983, Genetics 105: 357-70; 6 = The Seattle-La Jolla Drosophila Laboratories, 1971, DIS 47, Suppl. | 0 coordinate at the point of the insertion associated with en1. Minus values to the left; plus values to the right. / Dominant phenotype: Partial absence of abdominal markings ("erased"). ` Homozygous lethal. Enhances extra sex comb phenotype of Pc (Sato et al., 1983). # T(2;3)Es: see T(2;3)enEs # T(2;3)eve1.18: see Tp(2;3)eve1.18 # T(2;3)FC9 cytology: T(2;3)84D-86E-F;25F7-26A. references: Lehmann and Nusslein-Volhard, 1987, Dev. Biol. 119: 402-17. # T(2;3)FC10 cytology: T(2;3)35;84A-B;93D. references: Lehmann and Nusslein-Volhard, 1987, Dev. Biol. 119: 402-17. # T(2;3)fkh: Translocation (2;3) fork head cytology: T(2;3)38;98D2-3. origin: X ray induced. references: Jurgens and Weigel, 1988, Roux's Arch. Dev. Biol. 197: 345-54. genetics: Weak fkh phenotype. # T(2;3)FM27: see Tp(3;2)N2-27 # T(2;3)FM29: see T(2;3)N2-29 # T(2;3)FM46: see T(2;3)N2-46 # T(2;3)ftzRpl: Translocation (2;3) fushi-tarazu- regulator of postbithorax-like cytology: T(2;3)40-41;84B1-2. origin: X ray induced. discoverer: Duncan. synonym: T(2;3)Rpl. references: Weiner, Scott, and Kaufman, 1984, Cell 37: 843-51. Laughon and Scott, 1984, Nature 310: 25-31. Duncan, 1986, Cell 47: 297-304. genetics: Heterozygotes show transformations of posterior hal- tere to posterior wing. molecular biology: Encodes truncated protein in which the C- terminal amino acids are replaced by 10 novel amino acids (Laughon and Scott, 1984). Breakpoint on 3 lies within the homeobox of the ftz coding sequence. # T(2;3)G16: Translocation (2;3) Gelbart cytology: T(2;3)35D5-7;85F6-8;87F (Ashburner). new order: 21 - 35D5|85F6 - 61; 60 - 35D7|87F - 85F8|87F - 100. origin: X ray induced. discoverer: Gelbart. references: Ashburner, Tsubota, and Woodruff, 1982, Genetics 102: 401-20. genetics: 2L break associated with l(2)35Dd. # T(2;3)G24 cytology: T(2;3)35E1-2;89A1-2;92A1-2. new order: 21 - 35E1|89A2 - 92A1|89A1 - 61; 100 - 92A2|35E2 - 60. origin: X ray induced. discoverer: Gelbart. # T(2;3)G40 cytology: T(2;3)34F4-5;91E5-6. discoverer: Gelbart. genetics: Broken proximal to noc. # T(2;3)gl63d: Translocation (2;3) glass origin: / ray induced. discoverer: Ives, 63d29. references: 1965, DIS 40: 35. genetics: Mutant for gl. # T(2;3)Gla2: Translocation (2;3) Glazed-2 cytology: T(2;3)27-28;87-88. origin: X ray induced. references: The Seattle-La Jolla Drosophila Laboratories, 1971, DIS 47, Suppl. genetics: Associated with Gla2. # T(2;3)Gldd5: Translocation (2;3) Glucose dehydrogenase cytology: T(2;3)?;84C8-D1. references: Cavener, Otteson, and Kaufman, 1986, Genetics 14: 111-23. Cavener, Corbett, Cox, and Whitten, 1986, EMBO J. 5: 2939-48. genetics: Mutant for Gld. molecular biology: Distal breakpoint at about +134 kb on the molecular map of Cavener, Corbett, Cox, and Whetten. # T(2;3)gls: Translocation (2;3) glassy cytology: T(2;3)47B;91A. synonym: T(2;3)T2. references: Robinson and Curtis, 1972, Can. J. Genet. Cytol. 14: 129-37. genetics: Homozygotes viable and fertile, with abnormal eye. In heterozygotes T(2;3)gls/T(2;3)smg, females are more fertile than males. # T(2;3)Gr: see T(2;3)PuGr # T(2;3)GT origin: / ray induced. discoverer: Durrant. translocation cytology genetics ________________________________________________________________ T(2;3)GT3 ( 28B-C;35B1-2;41;42F;98D T(2;3)GT7 | 35B3;81;92F1-2 noc/osp T(2;3)GT8 35A1-4;62F3-6 + T(2;3)50B;81 l(2)35Ba noc T(2;3)GT10 34A1-4;76A5-7 l(2)34Fc/l(2)34Fd ( New order: 21 - 22C|41 - 35B1-2|28B-C - 22C|42F - 60; 61 - 98D|35B1-2 - 28B-C|42F - 41|98D - 100. | New order: 21 - 35B3|81 - 61; 60 - 35B3|92F1-2 - 81|92F1-2 - 100. # T(2;3)h: Translocation (2;3) hairy origin: X ray induced. genetics: Homozygous lethal. translocation cytology synonym ref ( _________________________________________________________ T(2;3)hm1 66D9-11;41A 1 T(2;3)hR40 |/ 30B7-C1;66D6-10;73B-C h+40 1, 2, 3 T(2;3)hR47 /` 23A2-B1;66D6-10 + h+47 1, 2, 3 34C2-4;98F12-99A1 ( 1 = Ingham, Pinchin, Howard, and Ish-Horowicz, 1985, Genetics 111: 463-86; 2 = Jeffery, 1971, DIS 47: 37; 3 = Jeffery, 1979, Genetics 91: 105-25. | New order: 21 - 30B7|73B - 66D10|73C - 100; 61 - 66D6|30C1 - 60. / Heterozygotes over h variegate for h (Jeffery, 1971). ` Molecular biology: 66D6 break located at -19.8 to -14.9 on the DNA map of h (Howard, Ingham, and Rushlow, 1988, Genes Dev. 2: 1037-46); "+" values to right, "-" values to left. The coordinate system has 0 at the start of transciption (Rushlow). #*T(2;3)h100.271 cytology: T(2;3)41;66D14-E1. origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42-54. genetics: Mutant for h. # T(2;3)H: Translocation (2;3) Hilliker origin: ( ray induced. references: Hilliker and Trusis-Coulter, 1987, Genetics 117: 233-44. Table I includes translocations available for complementation studies; Table II includes translocations that were lost and not available for complementation studies. Table I genetics translocation ( cytology (homozygotes) ___________________________________________________________________ T(2;3)H1 43F1-2;87D4-13 viable; fertile T(2;3)H2 38D-E;78B lethal T(2;3)H3| 42A6-19;83D5-E1 + lethal In(3R)84F12-16;98C3-D1 T(2;3)H4 25B-C;87B4-5 lethal T(2;3)H5 42B1-4;82C2-D1 lethal T(2;3)H6 21B2-8;82F8-83A1 lethal T(2;3)H7 24D2-E;78C lethal T(2;3)H8 40-41;98D1-2 viable; fertile T(2;3)H9 24D1-2;80-81 lethal T(2;3)H10 44C5-D1;84D3-8 viable; fertile T(2;3)H11 40-41;80-81 lethal T(2;3)H12 21E2-F1;83C2-D1 lethal T(2;3)H13 40-41;83E lethal T(2;3)H14 53D3-E1;79E2-5 viable; fertile T(2;3)H15 47B;92D3-9 viable; fertile T(2;3)H16 59C5-D1;80 viable; fertile T(2;3)H17 41;62D6-E2 lethal T(2;3)H18 51D2-7;96E5-9 semilethal; male sterile; female fertile T(2;3)H19 43B1-C1;87D3-E1 lethal T(2;3)H20 21B;74C viable T(2;3)H21| 46F5-47A1;87B + male sterile; In(2LR)34A;53D female sterile T(2;3)H22 40-41;80;81 viable; fertile T(2;3)H23| 25A2-4;71F2-72A2;98D1-2 lethal 60-25A|71F-61 T(2;3)H24 49C-D;81 semilethal; male sterile; female fertile T(2;3)H25 57A3-B1;87D1-2 viable; fertile T(2;3)H26 42B1-4;66A lethal T(2;3)H27 56F2-5;68C lethal T(2;3)H28 40;98F1-2 lethal T(2;3)H29 30C;80-81 lethal T(2;3)H30 21A;83D2-4 lethal T(2;3)H31 32D3-5;79F3-6 lethal T(2;3)H32| 44E;72F3-5; lethal 85F-86A;het T(2;3)H33 41;91F lethal T(2;3)H34 22F2-23A1;81 semilethal; fertile T(2;3)H35 40-41;80-81 viable; male sterile; female fertile T(2;3)H36 43B;83A lethal T(2;3)H37 41;98B semilethal; fertile T(2;3)H38 55F3-56A1;64F lethal T(2;3)H39 40-41;80-81 viable; fertile T(2;3)H40 40;95F lethal T(2;3)H41 40-41;80-81 viable; fertile T(2;3)H42 28A;81 lethal T(2;3)H43 42A;82F viable; fertile T(2;3)H44 28A;63E lethal T(2;3)H45 38B;80-81 semilethal; fertile T(2;3)H46 40-41;67E lethal T(2;3)H47 35A-B;65F viable; fertile T(2;3)H48 40-41;80-81 semilethal; fertile T(2;3)H49 47D4-8;88B lethal T(2;3)H50 35D;80-81 semilethal; fertile T(2;3)H51 38A1-2;78A1-2 semilethal; male sterile; female fertile T(2;3)H52 40-41;85E5-F1 lethal T(2;3)H53 36B2-C1;62B8-10 lethal T(2;3)H54 56C;70B viable; fertile T(2;3)H55 59C3-D3;81 lethal T(2;3)H56 45E;87E lethal T(2;3)H58 41;70A viable; male sterile; female fertile T(2;3)H61 22D;64C viable; fertile T(2;3)H62| 22F3-23A2;55E;66A8-20 lethal T(2;3)H63 58D;72D lethal T(2;3)H64 40-41;80-81 viable; fertile T(2;3)H65| 45B;50F;87C lethal T(2;3)H66| 24D3-5;85C;88B lethal T(2;3)H67 35B9-C2;80 lethal T(2;3)H68 35B-84B lethal T(2;3)H70 40-41;92E-F viable; male fertile; female low fertility T(2;3)H71| 41;87A + semilethal; In(2R)54D;59D male sterile; female fertile T(2;3)H72 41;65D viable; fertile T(2;3)H73 41;65F viable; fertile T(2;3)H74 41;93C lethal T(2;3)H75 58F;80-81 lethal T(2;3)H76 414;64E viable; fertile T(2;3)H77 33F3-5;82D viable; fertile T(2;3)H78 48C1-2;61C viable; sterile T(2;3)H80 41;87E lethal T(2;3)H82 45A2-C1;87D3-E1 lethal T(2;3)H83 27E-F;81 lethal T(2;3)H84 36C;67D1-9 viable; fertile T(2;3)H85 48F;85C lethal T(2;3)H86 33B;62A low viabilty; male sterile; female fertile T(2;3)H87| 23D;85C;87B semilethal; In(3R)85C;87B fertile T(2;3)H88 40-41;98C2-D2 lethal T(2;3)H89| 30A;35A;81 lethal T(2;3)H91 50C2-4;79D2-4 viable; fertile T(2;3)H93 57B14-C1;81 lethal T(2;3)H94 38B;71E lethal T(2;3)H95 36C;84B lethal T(2;3)H96 25E3-F1;80 lethal T(2;3)H97 49A-B;88F viable; fertile T(2;3)H98 30E-F;81 lethal T(2;3)H99 41;99A lethal T(2;3)H100 33B;86B lethal T(2;3)H102| 21F;2F;62F;63E lethal T(2;3)H103 43F2-44A2;94D4-E7 lethal T(2;3)H104 52D;65B lethal T(2;3)H105| 34C;71F + semilethal; 35B-70C T(2;3)H106 25E2-F2;80-81 semilethal; fertile T(2;3)H110 54C;95D lethal T(2;3)H111 30A2-7;65C1-2 viable; fertile T(2;3)H112| 29F;83E + 53C;66A + lethal Df(3R)81;96A T(2;3)H113 30A-80 lethal T(2;3)H114| 41F;57B + 57F;het lethal T(2;3)H116 42A2-B1;96C2-D1 lethal T(2;3)H117 23D;93E4-F2 viable; male sterile; female fertile T(2;3)H118 34C;80 semilethal; fertile T(2;3)H119 32F2-33A1;82D viable; fertile T(2;3)H120 40-41;80-81 + lethal In(3R)82C-D;90A2-B1 T(2;3)H122 36F;80-81 lethal T(2;3)H123 55C4-D1;80 lethal T(2;3)H124 48C;74B-C viable; fertile T(2;3)H125 41;75D1-2 lethal T(2;3)H126 48A2-B1;99F lethal T(2;3)H127 41;94D1-2 viable; fertile T(2;3)H128 53D;88D lethal T(2;3)H129 47A1-2;71C1-2 lethal T(2;3)H130 42B2-C1;80-81 viable; fertile T(2;3)H131 47A2-B1;84D4-9 lethal T(2;3)H132 41;97B6-C2 lethal T(2;3)H133 44D5-E1;64E lethal T(2;3)H136 57D;80-81 semilethal; male sterile; female fertile T(2;3)H137 40;84F12-85A1 lethal T(2;3)H139 25E1-2;75C1-2 lethal T(2;3)H140 33B;82C lethal T(2;3)H141 40-41;66B lethal T(2;3)H144 23A1-2;99A7-B1 lethal T(2;3)H147 34C3-6;80 viable; fertile T(2;3)H148 22D1-2;87D viable; fertile T(2;3)H151 48F;81 viable; fertile T(2;3)H152| 30A2-7;34D;99B5-C1 semilethal; male sterile; female fertile T(2;3)H153 37C2-D1;75A5-B2 lethal T(2;3)H154| 22A5-B1;25A;78E2-5 lethal T(2;3)H155| 60D1-2;93A1-2;98C1-2; lethal 100D2-E1 ( Synonym: T(2;3)1 - T(2;3)155. | New order: T(2;3)H3 = 21-42A|83D-84F|98C-84F|98C-100; 60|76A-83D|42A-60C|76A-61. T(2;3)H21 = 21-25A|98D-71F|98D-100; 60-25A|71F-61. T(2;3)H23 = 21-34A|53D-47A|87B-61; 60-53D|34A-46F|87B-100. T(2;3)H32 = 21-44E|72-61; het?|72F-85F|44E-60; het?|85F-100. T(2;3)H62 = 21-22F|66A-100; 60-55E|23A-55E|66A-61. T(2;3)H65 = 21-45B|87C-100; 61-87C|50C-45B|50F-60. T(2;3)H66 = 21-24D|85C-88B|85C-61; 60-24D|88B-100. T(2;3)H71 = 21-41; 87A-100; 60-54D|59D-54D|59D-41|87A-61. T(2;3)H87 = 21-23D|61-85C; 60-23D|87B-85C|87B-100. T(2;3)H89 = 21-30A|35A-30|81-61; 60-35A|81-100. T(2;3)H102 = 60-22F|62F-61; 21A-21F|63E-62F|21F-22F|63-100. T(2;3)H105 = 21C-34C|71F-100; 60-35B|70C-71F|34C-35B|70C-61. T(2;3)H112 = 21-29F|83E-81|96A-83E| 29F-53C|66A-61; 60-53C|60-53C|66A-81|96A-100. T(2;3)H114 = 21-41F|67B-61; het|57F-41F|67B-100; 60-57F|het. T(2;3)H152 = 21-30A|99B-61; 60-34D|30A-34D|99B-100. T(2;3)H154 = 21-22A|78E-100; 60-25A|22B-25A|78E-61. T(2;3)H155 = 21-60D|100D-100F; 60F-60D|93A-98C|100D-98C|83A-61. Table II translocation ( cytology genetics (homozygotes) __________________________________________________________________________ *T(2;3)H2a 41;100F2-5 lethal *T(2;3)H4a 50A10-15;90C8-D1 viable *T(2;3)H5a 41;63E3-8 lethal *T(2;3)H6a 60D6-9;94A1-3 + lethal In(3R)87D3-10;96F9-11 *T(2;3)H7a 40-41;57F;70C2-12;90C lethal *T(2;3)H8a 36C-D;83C2-4 not determined *T(2;3)H11a 36C2-E1;80-81 viable *T(2;3)H16a 56D2-E1;67C2-4 viable *T(2;3)H18a 31F2-32A1;81 not determined *T(2;3)H22a 40-41;80-81 lethal *T(2;3)H23a 40-41;72E2-F1 viable *T(2;3)H26a 57A2-4;65F2-66A1 lethal *T(2;3)H28a 41;88C10-E1 viable *T(2;3)H31a 38D;69F2-70A1 viable *T(2;3)H33a 40-41;82E2-7 not determined *T(2;3)H36a 33A1-B12;71F2-72A1 viable *T(2;3)H38a 50C11-20;80 viable *T(2;3)H40a 60F1-2;73A;het(?) lethal *T(2;3)H42a 38A2-C1;89A1-3;80 viable *T(2;3)H48a 22A1-2;81 lethal *T(2;3)H49a 35B2-9;80-81 viable *T(2;3)H50a 59E2;80-81 not determined *T(2;3)H51a 56C3-D1;82E7-8 lethal *T(2;3)H52a 40;99C3-D1 lethal *T(2;3)H54a 36C;80-81 viable *T(2;3)H55a 23A;98B-C lethal *T(2;3)H57a 51F;61C7-9 lethal *T(2;3)H61a 23E1-2;64E1-2;het lethal *T(2;3)H63a 42A;43F;99D2-4;het lethal *T(2;3)H65a 59D;64A12-B2 lethal *T(2;3)H66a 21D2-E1;80 viable *T(2;3)H67a 41;99A8-B1 lethal ( Synonym: T(2;3)LO2 - T(2;3)LO67 ("LD" = lost). # T2;3)H24: Translocation (2;3) Hairless cytology: T(2;3)41;92F1-2. references: Bang, Hartenstein and Posakony, 1991, Development 111: 89-104. genetics: Mutant for H. #*T(2;3)HK: Translocation (2;3) Half of Krivshenko cytology: T(2;3)22A;61A. origin: X ray induced in female. discoverer: Krivshenko, 56l14. references: 1959, DIS 33: 95. genetics: Only the 3P2LD element recovered from the treated oocyte. # T(2;3)Hm: Translocation (2;3) Haltere mimic cytology: T(2;3)29;32;88F;89E3-4. new order: 21 - 29|88F - 61; 60 - 32|88F - 89E3|29 - 32|89E4 - 100. origin: X ray induced. discoverer: Slatis, 49b5. references: Lewis, 1982, Embryonic Development: Genetic Aspects (Burger and Weber, eds.). Alan Liss, Inc., New York. Progress in Clin. Biol. Res. 85A: 269-89. genetics: Associated with CbxHm. # T(2;3)Hn: Translocation (2;3) Henna cytology: T(2;3)53E-54A;77A;94F;96A (Lewis). new order: 21 - 53E|77A - 61; 60 - 54A|94F - 96A|77A - 94F|96A - 100. Tentative. origin: X ray induced. discoverer: Van Atta, 30k. references: 1932, Am. Nat. 66: 93-95. 1932, Genetics 17: 637-59. genetics: Separable from Hn, which is associated with Df(3L)Hn = Df(3L)66A;66B. # T(2;3)ho5: see T(2;3)dpp3 # T(2;3)HR origin: X ray induced. genetics: Crossover suppressor between h and ri. homozygous translocation cytology ref ( viability __________________________________________________________ T(2;3)HR17 26A;69F 1 - T(2;3)HR26 28A;64D 1 - T(2;3)HR28 25A;91D + 42A;71A-B 1 - T(2;3)HR30 | 34E1-3;70C1-2 1, 2, 3 + ( 1 = Ashburner, 1972, DIS 49: 34; 2 = Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91; 3 = Craymer, 1981, Genetics 99: 75-97. | Also fertile and wild type. # T(2;3)I: Translocation (2;3) Ising discoverer: Ising. references: Ashburner. translocation cytology _______________________________________________ T(2;3)I805 40F;75AB + In(3R)89;94 T(2;3)I806 55E;66A T(2;3)I810 53F;95E-F # T(2;3)iab445: Translocation (2;3) infraabdominal cytology: T(2;3)32;41;89E. Complex. origin: X ray induced. discoverer: R.H. Baker. genetics: Mutant for iab4. molecular biology: 89E breakpoint 78.5-82 kb to the right of right breakpoint of In(3R)Cbxrv1. # T(2;3)iab6 origin: X ray induced. genetics: Mutant for iab6. molecular translocation cytology discoverer biology ( _______________________________________________________ T(2;3)iab675 30A-B;31D-E; Baker 103--108 kb 59F;89E;89F T(2;3)iab6105 60C;89E Lewis 108-111 kb T(2;3)iab6C1 60B;81;89E; Crosby 108-111 kb ( Coordinates of 89E breakpoints in kilobases to the right of the right breakpoint of In(3R)Cbxrv1. # T(2;3)iab8rv genetics: Revertants of iab8 in the BXC. translocation cytology _____________________________ T(2;3)iab8rv100 37E-38A;89E T(2;3)iab8rv185 50D;89E # T(2;3)iab965 cytology: T(2;3)41;89E. origin: X ray induced. discoverer: R.H. Baker. references: Karch, Weiffenbach, Peifer, Bender, Duncan, Cel- niker, Crosby, and Lewis, 1985, Cell 43: 81-96. Sanchez-Herrero, Vernos, Marco, and Morata, 1985, Nature 313: 108-13. Tiong, Bone, and Whittle, 1985, Mol. Gen. Genet. 200: 335-42. genetics: Mutant for iab9. molecular biology: 89E breakpoint 163-166.5 kb to the right of the right breakpoint of In(3R)Cbxrv1. # T(2;3)IC67-98 cytology: T(2;3)24E-F;91D. origin: X ray induced. references: Brosseau, 1969, DIS 44: 45. genetics: Homozygous lethal. # T(2;3)in60i2: Translocation (2;3) inturned cytology: T(2;3)62D-F;77B;80C. Complex translocation with inversion(s) in 3L. references: Arajarvi and Hannah-Alava, 1969, DIS 44: 73-74. genetics: Associated with in60i2. # T(2;3)Ir: Translocation (2;3) Irish cytology: T(2;3)55D-E;98F. origin: / ray induced. discoverer: Irish. other information: Induced along with Df(2L)dpp43. # T(2;3)JHT1 cytology: T(2;3)34C;96F. origin: Spontaneous in JH chromosome line during successive backcross programs. references: Yamaguchi and Mukai, 1974, Genetics 78: 1209-21. # T(2;3)JHT2 cytology: T(2;3)56F;97B. origin: Spontaneous in JH chromosome line during successive backcross programs. references: Yamaguchi and Mukai, 1974, Genetics 78: 1209-21. # T(2;3)L141 origin: / ray induced in T(Y;2)L141/+ males. discoverer: Lyttle. translocation cytology _____________________________ T(2;3)L141-2 36B;61B T(2;3)L141-3 40-41;80-81 T(2;3)L141-4 35D;79F T(2;3)L141-5 40-41;84F-85A T(2;3)L141-6 40-41;80-81 T(2;3)L141-7 42A;68D-E T(2;3)L141-8 40-41;80-81 T(2;3)L141-9 33C-D;83D-E T(2;3)L141-10 40-41;80-81 T(2;3)L141-11 40-41;80-81 T(2;3)L141-12 53C;64B T(2;3)L141-13 52D;87F T(2;3)L141-14 27E;86C T(2;3)L141-15 35B;80-81 T(2;3)L141-17 23C;70F-71A T(2;3)L141-18 51A;80C T(2;3)L141-19 40-41;85D T(2;3)L141-21 57E;94E T(2;3)L141-22 50C5-10;69E T(2;3)L141-23 35B;80-81 T(2;3)L141-24 22B3-6;98E T(2;3)L141-25 40-41;62F T(2;3)L141-26 34D;87D-E T(2;3)L141-28 43D5;75C4 T(2;3)L141-29 58E;64B-C T(2;3)L141-30 47E-F;80-81 T(2;3)L141-31 57A;87C T(2;3)L141-32 58D;61E T(2;3)L141-33 40-41;97D T(2;3)L141-34 55B;76B T(2;3)L141-36 37B;80-81 T(2;3)L141-37 40-41;80-81 T(2;3)L141-38 45A;65E-F T(2;3)L141-39 26B-C;98F T(2;3)L141-40 53E-F;82C-D T(2;3)L141-41 41;80 T(2;3)L141-43 40-41;80-81 T(2;3)L141-44 40;61E T(2;3)L141-45 57D2-4;78A T(2;3)L141-46 40-41;86E T(2;3)L141-47 60C-D;64E T(2;3)L141-48 38D;80-81 T(2;3)L141-49 24F;96E T(2;3)L141-50 41;98F T(2;3)L141-51 21C5;97D3 T(2;3)L141-52 40-41;93A T(2;3)L141-53 24F;61E-F # T(2;3)LD28 cytology: T(2;3)52A-C;81F. discoverer: De Jongh. # T(2;3)ltm Translocation origin: X ray induced. discoverer: Hessler, 1957. references: 1958, Genetics 43: 395-403. genetics: Variegated for lt. translocation cytology _________________________________________ *T(2;3)ltm1 40B-F;63E-F *T(2;3)ltm4 40B-F;67E *T(2;3)ltm5 40B-F;98C *T(2;3)ltm6 ( 26E-F;40B-F;96E T(2;3)ltm7 40B-F;100F *T(2;3)ltm8 40B-F;92B *T(2;3)ltm10 40B-F;64E *T(2;3)ltm11 40B-F;96F *T(2;3)ltm13 40B-F;64F *T(2;3)ltm14 40B-F;95F *T(2;3)ltm15 40B-F;92E *T(2;3)ltm17 40B-F;95C-D *T(2;3)ltm18 40B-F;98A *T(2;3)ltm19 40B-F;94B *T(2;3)ltm21 40B-F;93D *T(2;3)ltm23 40B-F;62F *T(2;3)ltm24 | 40B-F;59F;75C *T(2;3)ltm27 40B-F;88E-F *T(2;3)ltm28 40B-F;97E T(2;3)ltm29 40B-F;99F *T(2;3)ltm30 40B-F;99C *T(2;3)ltm32 40B-F;97A *T(2;3)ltm34 40B-F;61B *T(2;3)ltm35 40B-F;64C ( New order: 21 - 26E|40B - 26F|96E - 61; 60 - 40F|96E - 100. | New order: 21 - 40B|75C - 100; 60 - 59F|40F - 59F|75C - 61. # T(2;3)ltm100 cytology: T(2;3)40;97F. origin: X ray induced. references: Baker and Rein, 1962, Genetics 47: 1399-1407. genetics: Variegated for lt. Homozygous lethal. # T(2;3)ltx13 cytology: T(2;3)40F;97D2. discoverer: Wakimoto. references: James, Eissenberg, Craig, Dietrich, Hobson, and Elgin, 1989, Eur. J. Cell Biol. 50: 170-80. # T(2;3)MV54d: see T(2;3)MV #*T(2;3)Me2 origin: X ray induced. discoverer: Moore, 1929. references: Glass, 1933, J. Genet. 28: 69-112. genetics: Break in 2L near centromere. Mutant for Me. #*T(2;3)MeSo: Translocation (2;3) Moir' of Sytko discoverer: Sytko. references: Agol, 1936, DIS 5: 7. genetics: Breaks reportedly in 2R and 3R, yet mutant for Me in 3L. # T(2;3)Met: Translocation (2;3) Metatarsi irregular origin: X ray induced. discoverer: Jonsson, 56a10. references: 1956, DIS 30: 73. genetics: Associated with Met. # T(2;3)Mg: Translocation (2;3) Mglinetz translocation cytology origin ( ref | ___________________________________________ T(2;3)Mg15 31B;64A 1 2 T(2;3)Mg22 40;61F 1 3 T(2;3)Mg23 40;96A 1 3 T(2;3)Mg24 40;73F 1 3 T(2;3)Mg51 47D;93B 1 3 T(2;3)Mg52 25A;81F 1 3 T(2;3)Mg53 51F;94E 1 3 T(2;3)Mg54 60A;81F 1 3 T(2;3)Mg64 59D;68A 1 1 T(2;3)Mg166 23C;75C 1 1 T(2;3)Mg167 44A;87A 1 1 T(2;3)Mg168 55F;76E 1 1 T(2;3)Mg169 56E;91F 1 1 T(2;3)Mg170 48B;67C 1 1 T(2;3)Mg171 24F;74B 1 1 T(2;3)Mg172 32C;77B 1 1 T(2;3)Mg173 34A;82F 1 1 T(2;3)Mg174 53D;97B 1 1 T(2;3)Mg175 44F;99B 1 1 T(2;3)Mg176 31B;94D 1 1 T(2;3)Mg177 26B;71C 1 1 T(2;3)Mg178 50C;82A 1 1 T(2;3)Mg179 34A;79B 1 1 T(2;3)Mg180 28C;95F 1 1 T(2;3)Mg181 56E;78F 1 1 T(2;3)Mg182 45F;74B 1 1 T(2;3)Mg183 27C;62A 2 1 T(2;3)Mg184 28F;94A 2 1 T(2;3)Mg185 31B;87F 2 1 T(2;3)Mg186 43A;85B 2 1 T(2;3)Mg187 49E;92E 2 1 T(2;3)Mg188 35A;71C 2 1 T(2;3)Mg189 53C;88B 2 1 T(2;3)Mg190 39F;89E 2 1 T(2;3)Mg191 57D;99B 2 1 T(2;3)Mg192 26B;98F 2 1 T(2;3)Mg193 37F;84A 2 1 T(2;3)Mg194 55C;70C 2 1 T(2;3)Mg195 59D;83D 2 1 T(2;3)Mg196 50E;72C 2 1 ( 1 = / ray induced; 2 = 32P feeding. | 1 = Mglinetz, 1968, Genetika (Moscow) 4(8): 81-86; 2 = Mglinetz, 1971, Genetika (Moscow) 7(8): 108-14; 3 = Mglinetz, 1972, Genetika (Moscow) 8(2): 82-91. # T(2;3)ML origin: X ray induced. references: Mukhina and Zhimulev, 1980, DIS 55: 209. homozygous translocation cytology viability _____________________________________________ T(2;3)ML2 53A1;66C1 - T(2;3)ML3 34C6-7;70A4-5 - T(2;3)ML4 40-41;80-81 - T(2;3)ML5 41A;62B - T(2;3)ML8 40-41;80-81 - T(2;3)ML9 44C-D;64C - T(2;3)ML14 40-41;80-81 - T(2;3)ML76 32E;70A - T(2;3)ML122 21F;82E - T(2;3)ML192 ( 41;97A + 52B;86D - T(2;3)ML193 52E1;80-81 + - In(3R)93E;100F T(2;3)ML225 53C;96C + T(2;3)ML270 40-41;80-81 - T(2;3)ML307 | 50D1;79A - T(2;3)ML348 35C;70A - T(2;3)ML393 40B;63A - T(2;3)ML405 57A;92E - T(2;3)ML436 40-41;80-81 - T(2;3)ML443 / 24D;87C1 - T(2;3)ML457 40-41;80-81 + - Df(3R)87A;87C T(2;3)ML460 39E;75C + T(2;3)ML464 39E;61D - T(2;3)ML466 40-41;80-81 - T(2;3)ML472 32E;96F - T(2;3)ML474 35B3-5;94D5-13 - T(2;3)ML478 40-41;80-81 - T(2;3)ML484 40-41;80-81 - T(2;3)ML486 39E;90D + T(2;3)ML488 40-41;80-81 - T(2;3)ML490 27E;92B1 - T(2;3)ML491 40-41;80-81 + T(2;3)ML494 60E6;99C1 - T(2;3)ML495 22B1;81F - T(2;3)ML498 35A;87F - T(2;3)ML499 40-41;80-81 - T(2;3)ML501 50A;64E + T(2;3)ML502 40-41;80-81 - T(2;3)ML505 21B;97C - T(2;3)ML506 ` 55C;85C - T(2;3)ML507 40-41;80-81 - T(2;3)ML508 40-41;80-81 - T(2;3)ML509 40-41;80-81 - T(2;3)ML510 40-41;80-81 - T(2;3)ML511 40-41;80-81 - T(2;3)ML512 40-41;80-81 - T(2;3)ML514 40-41;80-81 - ( New order: 21 - 41|97A - 86D|52B - 60; 61 - 86D|52B - 41|97A - 100. | L4 interrupted. / Extra veins. ` L2 and L4 veins thin. #*T(2;3)MO origin: Spontaneous. discoverer: Imaizumi, 59a. references: 1962, Cytologia 27: 212-28. genetics: Breaks between cn and vg in 2R and between st and ss in 3R. # T(2;3)Mot-K: Translocation (2;3) Mottled of Krivshenko cytology: T(2;3)41;60D;80-81; breakpoint in chromosome 3 with respect to centromere not determined; association of arms therefore ambiguous. new order: 21 - 41|80 - 61; 60F - 60D|41 - 60D|80 - 100. Tentative. origin: X ray induced. discoverer: Krivshenko, 54c25. references: 1954, DIS 28: 75. 1955, DIS 29: 76. genetics: Associated with Mot-K. Homozygous lethal. # T(2;3)MP: Translocation (2;3) Mamon Petrukhina origin: X ray induced. references: Mamon, Petrukhina, Rasheva, and Vatti, 1977, Genetika (Moscow) 13(8): 1378-86. translocation cytology __________________________________ T(2;3)MP3 56C;89A T(2;3)MP4 56-57;62E T(2;3)MP5 28B-C;98B-C T(2;3)MP6 38B;77D-E T(2;3)MP9 40-41;80-81 T(2;3)MP10 26D-E;66A-B T(2;3)MP15 40-41;80-81 T(2;3)MP19 43B-C;96C T(2;3)MP19a 31E-F;69D-E T(2;3)MP22 33F;65C T(2;3)MP26 49B-C;92D-E T(2;3)MP28 50A;85D-F T(2;3)MP35 38A;84C-D T(2;3)MP37 50B-C;66D-E T(2;3)MP41 40-41;80-81 T(2;3)MP42 40-41;80-81 T(2;3)MP44 52F;96B T(2;3)MP46 28A-B;78D T(2;3)MP47 40-41;80-81 T(2;3)MP48 48C-D;80-81 T(2;3)MP55 21B;61A T(2;3)MP63 52D-E;95-96 T(2;3)MP64 40-41;70A T(2;3)MP65 30-31;79A T(2;3)MP69 23D;87A-B T(2;3)MP72 33A-B;80-81 T(2;3)MP74 41-42;98 T(2;3)MP75 50A-B;100C T(2;3)MP78 40-41;80-81 T(2;3)MP80 53B;97C-D T(2;3)MP81 40-41;80-81 T(2;3)MP84 50-51;97-98 T(2;3)MP85 52;86-87 T(2;3)MP87 27A-B;96C-D T(2;3)MP100 39C;84A-B T(2;3)MP101 40-41;80-81 T(2;3)MP104 40-41;80-81 T(2;3)MP108 40-41;80-81 T(2;3)MP109 50A;81-82 T(2;3)MP110 35D-E;70-71 T(2;3)MP111 40-41;80-81 T(2;3)MP112 40C-F;98D-F T(2;3)MP113 40-41;80-81 T(2;3)MP114 49B;65-66 T(2;3)MP115 40-41;80-81 # T(2;3)Mpe: Translocation (2;3) Monoplane cytology: T(2;3)35B2-3;86C1-2 (Ashburner). origin: X ray induced. discoverer: Shelton. references: Hughes and Shelton, 1980, DIS 55: 204-05. Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Lit- tlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689-706. McGill, Chia, Karp, and Ashburner, 1988, Genetics 119: 647- 61. genetics: Associated with dominant Mpe phenotype and recessive osp allele. Also shows a dominant leg phenotype (thickening of the tibial-tarsal joint of the metathoracic leg). Pheno- types of leg and outstretched-wing associated with 2P3D ele- ment of the translocation. Lethal homozygous or with Df(3R)cu40 and Df(3R)by77. Heterozygotes show reduced viabil- ity and partial sterility (Hughes and Shelton, 1980). T(2;3)Mpe heterozygous with a deletion of the entire noc region is noc+ (McGill et al., 1988). molecular biology: 35B2-3 breakpoint at -103 to -106.5 bp in the molecular map of the wild-type noc-Adh region (McGill et al., 1988) (coordinate 0 on EcoR1 restriction site 1321 bp to the left of the start of transcription of the larval Adh tran- script, "+" values to the right, "-" values to the left). # T(2;3)MscT3: Translocation (2;3) Multiple sex comb origin: / ray induced. discoverer: Tiong. references: Kennison and Russell, 1987, Genetics 116: 75-86. genetics: Mutant for Msc. #*T(2;3)MV: Translocation (2;3) Variegated of Mickey cytology: T(2;3)43E;75C. origin: / ray induced. discoverer: Mickey, 54d. synonym: T(2;3)MV54d. references: 1963, DIS 38: 30. genetics: Eye color variegated, more prominent in male. # T(2;3)N origin: X ray induced. genetics of translocation cytology ref ( homozygotes _________________________________________________________________________ T(2;3)N1-14 32C2-D1;99F6-100A1 2 viable, female sterile T(2;3)N1-15 56A2-B1;70A-B 2 viable T(2;3)N1-17 28D4-E1;72E2-73A1 2 poorly viable T(2;3)N1-18 38B;77A2-B1 2 lethal *T(2;3)N1-20 23E;86E2-7 2 poorly viable T(2;3)N1-23 40-41;80-81 2 viable, sterile T(2;3)N1-25 36B-D;84D 2 lethal *T(2;3)N2-28 36E-F;80B-C 2 lethal T(2;3)N2-29 | 40-41;80-81 1, 2, 3, 4 viable, sterile T(2;3)N2-32 / 48B;71C1-2;89C 2 lethal T(2;3)N2-33 23C-D;90C-D 2 lethal *T(2;3)N2-34 / 37D-E;65;70 + 2 dominant female Dp(3L)65;70 sterile T(2;3)N2-41 / 23A2-B3;24F-25A1;96A23-B1 2 poorly viable T(2;3)N2-46 ` 40-41;80-81 1, 2, 3, 4 viable, fertile T(2;3)N2-48 57E2-F1;98C 2 lethal ( 1 = Puro, 1973, Hereditas 75: 140-43; 2 = Puro, 1982, DIS 58: 205-08; 3 = Puro, 1985, Genet. Res. 46: 287-307; 4 = Puro and Kiiskila, 1982, DIS 58: 125-26. | Synonym: T(2;3)FM29. / New order: T(2;3)N2-32 = 21 - 48B|71C1 - 61; 60 - 48C|89C2 - 71C2|89D - 100. T(2;3)N2-34 = 21 - 37D|65 - 100; 61 - 69|37E - 60. T(2;3)N2-41 = 21 - 23A2|96A23 - 61; 60 - 25A1|23B3 - 24F|96B1 - 100. ` Synonym: T(2;3)FM46. # T(2;3)net18: Translocation (2;3) net cytology: T(2;3)27E-F;65A + In(2LR)net18 = In(2LR)21B3-4;42C- D1; small deficiency at distal end of 2L. origin: X ray induced. references: Golubovsky, Kulakov and Korochkina, 1978, Genetika 14(2): 294-305. Korochkina and Golubovsky, 1978, DIS 53: 197-200. genetics: Deficient for net and lgl but not al. Homozygous lethal and Minute. #*T(2;3)Nu: Translocation (2;3) Nude cytology: T(2;3)24;36-37;39-40;73-74;75-76;77-78;81-82;85- 86;89-90. origin: X ray induced. discoverer: Sutton, 41a27. references: CP627. genetics: Associated with Nu. Homozygous lethal. # T(2;3)odd3.29: see Tp(2;3)odd3.29 # T(2;3)osp90: Translocation (2;3) outspread cytology: T(2;3)35B3-4;89B9-11. origin: / ray induced. discoverer: Detwiler. references: Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689-706. genetics: Associated with osp90. molecular biology: Breakpoint on 2 between 14 and 18 kilobases to the right of the EcoRI restriction site immediately distal to Adh (Chia et al.). # T(2;3)p4: Translocation (2;3) pink cytology: T(2;3)34D;84D6-10;85A1-2. Deficient for 84D6-10 to 85A1-2. origin: X ray induced. references: Kemphues, Raff, Raff, and Kaufman, 1980, Cell 21: 445-51. Kemphues, Raff, and Kaufman, 1983, Genetics 105: 345-56. genetics: Deficient for p. # T(2;3)pXT126 cytology: T(2;3)44F;85A. origin: X ray induced. references: Lehmann and Nusslein-Volhard, 1987, Wilhelm Roux's Arch. Dev. Biol. 119: 402-07. genetics: Mutant for p. # T(2;3)P: Translocation (2;3) Pasadena origin: X ray induced. discoverer: E.B. Lewis. translocation cytology ref ( ___________________________________ T(2;3)P3 40;88B 4 T(2;3)P8 | 48C1-2;84D 2 T(2;3)P15 60E;86C-D 1 T(2;3)P23 / 56F;81F 5 T(2;3)P49 57D;81F 4 T(2;3)P58 41;89E 4 T(2;3)P71 60E;81F 2 T(2;3)P89 36-39;86E11 3 ( 1 = Craymer; 2 = Craymer, 1984, Genetics 108: 573-87; 3 = Ellgaard and Brosseau, 1969, Genetics 62: 337-41; 4 = Holm, 1976, The Genetics and Biology of Drosophila (Ash- burner and Novitski, eds.). Academic Press, London, New York, San Francisco, Vol. 1b, pp. 529-61; 5 = Lewis, 1963, Am. Zool. 3: 33-56. | Induced with In(3L)63A-C;78F (E.B. Lewis). / T(2;3)P23, Ubx/bx34e heterozygote shows transvection effect. # T(2;3)pb3: Translocation (2;3) proboscipedia cytology: T(2;3)35B2-3;83E2-8;89A9-10 + T(2;3)50C14;80 (Ash- burner). new order: 21 - 35B2|83E8 - 89A9|83E2 - 80|50C14 - 60; 61 - 80|50C14 - 35B3|89A10 - 100. origin: X ray induced. references: Kaufman, 1978, Genetics 90: 579-96. Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Lit- tlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689-706. genetics: Homozygous lethal. Associated with osppb3, a viable recessive osp allele at 35B (Ashburner et al., 1981). molecular biology: Breakpoint proximal to Adh by molecular cri- teria (McGill). # T(2;3)Pcl Translocation (2;3) Polycomblike cytology: T(2;3)55A;80 (Kennison). origin: / ray induced in a mwh iab9tuh3 stock. discoverer: Tiong. genetics: Associated with Pcl. Breakpoint in 3L proximal to ri+. # T(2;3)prd2.27: see Tp(2;3)prd2.27 #*T(2;3)Pu: Translocation (2;3) Punch cytology: T(2;3)41A;70D-E + T(2;3)57B5-C1;79F. new order: 21 - 41A|70E - 79F|57C1 - 60; 61 - 70D|41A - 57B5|79F - 100. Tentative. origin: X ray induced. discoverer: Oliver, 28k4. references: Muller, 1930, J. Genet. 22: 326. Oliver, 1932, Z. Indukt. Abstamm. Vererbungsl. 61: 484. genetics: Associated with Pu. Homozygous lethal. # T(2;3)PuGr: Translocation (2;3) Punch-Grape cytology: T(2;3)57C;81F (Lewis, 1956, DIS 30: 130). origin: X ray induced. discoverer: Muller, 29l. synonym: T(2;3)Gr: Translocation (2;3) Grape; T(2;3)pGr: Translocation (2;3) pink-Grape. references: Glass, 1933, J. Genet. 28: 69-112. 1934, Am. Nat. 68: 107-14. Mackay and O'Donnell, 1983, Genetics 105: 35-53. genetics: Mutant for Pu, showing dominant variegated eye color. Homozygous lethal. # T(2;3)PuH16 cytology: T(2;3)57C3-9;63B. origin: / ray induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Mutant for Pu. #*T(2;3)Purv: Translocation (2;3) Punch-reverted cytology: T(2;3)40F-41A;70D-E + T(2;3)57B5-C1;79F. new order: 21 - 40F|70E - 79F|57B5 - 41A1|70D - 61; 60 - 57C1|79F - 100. Tentative. origin: X-ray-induced derivative of T(2;3)Pu = T(2;3)40F- 41A;70D-E + T(2;3)57B5-C1;79F. discoverer: Oliver, 32l27. references: 1939, Genetics 24: 82. 1941, Proc. Intern. Congr. Genet., 7th., p. 228. genetics: Partial reversal of Pu. Homozygous lethal. # T(2;3)PuW: Translocation (2;3) Punch-Wine cytology: T(2;3)57C4-6;80. origin: X ray induced. discoverer: E.B. Lewis, 55h. references: Mackay and O'Donnell, 1983, Genetics 105: 35-53. genetics: Mutant for Pu, showing dominant variegated eye color. Homozygous lethal. # T(2;3)RBR37 cytology: T(2;3)26A;88F. origin: Spontaneous [accumulated on second chromosome lines during repeated backcrossing of In(2LR)bwV1/+ males to In(2LR)bwV1/SM1 females]. references: Yamaguchi, Cardellino, and Mukai, 1976, Genetics 83: 409-22. # T(2;3)RBR77 cytology: T(2;3)33B;99F. origin: Spontaneous [accumulated on second chromosome lines during repeated backcrossing of In(2LR)bwV1/+ males to In(2LR)bwV1/SM1 females]. references: Yamaguchi, Cardellino, and Mukai, 1976, Genetics 83: 409-22. # T(2;3)rg35 cytology: T(2;3)27E-F;62C2-D1. origin: / ray induced. Sliter, Henrioh, Tucker, and Gilbert, 1989, Genetics 123: 327-36. # T(2;3)ri60b2: Translocation (2;3) radius incompletus cytology: T(2;3)?;77E3-78A1. origin: X ray induced. references: Arajarvi and Hannah-Alava, 1969, DIS 44: 73-74. genetics: Mutant for ri. # T(2;3)rn: Translocation (2;3) rotund cytology: T(2;3)40-41;80-81;84D8-9 (Duncan and Kaufman, 1978; B.S. Baker). Configuration is 2L.3L;2R.3R (Puro and Kiiskila, 1982). new order: 21 - 40|80 - 61; 60 - 41|84D8 - 81F|84D9 - 100. Tentative. origin: Probably X ray induced. discoverer: Glass, 1929. references: 1934, DIS 2: 8. Muller, 1953, DIS 27: 106-7. Carlson, 1956, DIS 30: 109. Duncan and Kaufman, 1975, Genetics 80: 733-52. Puro and Kiiskila, 1982, DIS 80: 125-26. genetics: Mutant for rn. Homozygous viable and sterile in both sexes. About 10% of the progeny of parents heterozygous for T(2;3)rn and chromosome 2 inversions are nondisjunctional for chromosome 2 (Muller, 1953). # T(2;3)Rpl: see T(2;3)ftzRpl # T(2;3)RY2 origin: X ray induced. discoverer: Simpson. genetics: Deficient for sna. #*T(2;3)SL: Translocation (2;3) Star of Lewis cytology: T(2;3)21D;81;88D (Craymer, 1984). new order: 21A - 21D|81F - 88D|81F - 61; 60 - 21D|88D - 100. Tentative. origin: X ray induced. discoverer: E.B. Lewis, 1940. references: 1945, Genetics 30: 137-66. Craymer, 1984, Genetics 108: 573-87. genetics: Mutant for S. # T(2;3)SM: Translocation (2;3) Star of Muller cytology: T(2;3)21E2-3;79D2-E1 superimposed on In(2L)22D1- 2;33F5-34A1 + In(2R)42A2-3;58A4-B1. origin: X ray induced in In(2L)Cy + In(2R)Cy. discoverer: Muller, 1928. references: Painter and Muller, 1929, J. Heredity 20: 287-98. Muller, 1930, J. Genet. 22: 335-57. Morgan, Bridges, and Schultz, 1936, Year Book - Carnegie Inst. Washington 35: 293. genetics: Mutant for S; also carries Cy. # T(2;3)S9 cytology: T(2;3)40-41;80-81. origin: X ray induced. references: Sandler, Lindsley, Nicoletti, and Trippa, 1968, Genetics 60: 525-58. genetics: Homozygous lethal. #*T(2;3)Sa: Translocation (2;3) Salmon origin: X ray induced. discoverer: Van Atta, 30k1. references: 1932, Am. Nat. 66: 93-95. 1932, Genetics 17: 637-59. genetics: Associated with Sa. Homozygous lethal. Break in 2L between pr and centromere and in 3L near centromere. # T(2;3)SbV: Translocation (2;3) Stubble-Variegated cytology: T(2;3)41A-C;88;89B superimposed on In(3R)93D7- E1;98F2-6. In(3LR)P35 = In(3LR)65;83D-E induced simultane- ously but was separated from it by recombination. new order: 21 - 41A|89B - 93D7|98F2 - 93E1|98F6 - 100; 61A - 88|89B - 88|41C - 60. origin: X ray induced in In(3R)Mo, Sb sr. discoverer: E.B. Lewis, 1948. references: 1956, DIS 30: 76-77. genetics: Variegates for phenotype of deficiency for Sb, which is normal. # T(2;3)sbd47: Translocation (2;3) stubbloid cytology: T(2;3)41;89B10-12. origin: X ray induced. references: Spillman and Nothinger, 1978, DIS 53: 164-65. genetics: Associated with sbd47. Homozygous lethal. # T(2;3)sbd106 cytology: T(2;3)22E;89B. origin: X ray induced. discoverer: E.B. Lewis. #*T(2;3)Scar: Translocation (2;3) Scarred cytology: T(2;3)27E;95A + In(3R)91F;96A. origin: X ray induced. discoverer: Yu, 48h. references: 1949, DIS 23: 65. genetics: Associated with Scar. # T(2;3)Scorv7: Translocation (2;3) scutoid-revertant cytology: T(2;3)35D1-2;93F11-94A4 superimposed on Tp(2;2)Sco. new order: 21 - 35A4|(35C2 - 35C5)|35B4 - 35C1| 35B3 - 35B1|93F11 - 61; 60 - 35D2|93A4 - 100. origin: X ray induced. discoverer: Ashburner. references: Woodruff and Ashburner, 1979, Genetics 92: 117-32. Ashburner, Faithfull, Littlewood, Richards, Smith, Velis- sariou, and Woodruff, 1980, DIS 55: 193-95. Ashburner, Detwiler, Tsubota, and Woodruff, 1983, Genetics 104: 405-31. Ashburner and Harrington, 1984, Chromosoma 89: 329-37. genetics: Homozygous lethal. Revertant for Sco. # T(2;3)Scorv13 cytology: T(2;3)35D1-2;71B1-2;81. new order: 21 - 35A4|(35C2 - 35C5)|35B4 - 35C1|35B3 - 35B1| 71B2 - 81|71B1 - 61; 60 - 35D2|81 - 100. origin: X ray induced. discoverer: Ashburner. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. Ashburner, Detwiler, Tsubota, and Woodruff, 1983, Genetics 104: 405-31. Ashburner and Harrington, 1984, Chromosoma 89: 329-37. genetics: Homozygous lethal. 2L breakpoint maps between tran- sposed noc allele and sna. molecular biology: 35D1--2 breakpoint mapped to the DNA (McGill, Chia, Karp, and Ashburner, 1988, Genetics 119: 647- 61). # T(2;3)ScrT3: Translocation (2;3) Sex combs reduced cytology: Complex with breakpoints in at least 25C-D;84B1-2;92A (Kennison). origin: / ray induced in a mwh iab9tuh3 stock. discoverer: Tiong. genetics: Dfd+ Scr- ftz+ Antp+; associated with ScrT3. # T(2;3)ScxWrv1: Translocation (2;3) sex combs extra revertant cytology: T(2;3)58F1-2;84B1-2. origin: X ray induced. references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. Scott, Weiner, Hazelrigg, Polisky, Pirrotta, Scalenghe, and Kaufman, 1983, Cell 35: 763-76. genetics: Homozygous lethal; heterozygotes show reduced sex comb phenotype. Fails to complement Antp and certain Scr alleles for lethality; viable or semilethal with other Scr alleles. molecular biology: Third-chromosome breakpoint 79 kilobases to the right of the proximal breakpoint of Tp(3;3)Dfdrv16 (Scott et al., 1983). # T(2;3)ScxWrv6 cytology: T(2;3)22D1;63A1-2 + T(2;3)54A1-2;80-81. Pairing of polytene chromosomes in proximal 3R usually disrupted. synonym: T(2;3)ScxW+RX6. origin: X ray induced. references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. Scott, Weiner, Hazelrigg, Polisky, Pirrotta, Scalenghe, and Kaufman, 1983, Cell 35: 763-76. genetics: Homozygous lethal; heterozygotes show reduced sex comb phenotype. Fails to complement Scr and Antp for lethal- ity. # T(2;3)SD: Translocation (2;3) Segregation Distorter origin: X ray induced in SD-72 males. references: Yamazaki and Thompson, 1973, Jpn. J. Genet. 48: 217-29. genetics: Associated with SD. K values tested. translocation cytology synonym _______________________________________ T(2;3)SD-1 25D;61E T(2;3)SD72-9 T(2;3)SD-2 56;94 T(2;3)SD-182 T(2;3)SD-3 40-41;97 T(2;3)SD-392 # T(2;3)shvS: Translocation (2;3) shortvein of Segal references: Segal and Gelbart, 1985, Genetics 109: 119-43. genetics: Associated with shv alleles. Lethal over shv and other dpp lethals. translocation cytology origin ________________________________________________________ T(2;3)shvS1 ( 22F1-2;64E1-2 X ray T(2;3)shvS13 22F1-2;93B8-10 / ray T(2;3)shvS18 22F1-2;88E1-4 / ray T(2;3)shvS19 | 22F1-2;35A1-4;97A / ray T(2;3)shvS24 / 22F1-2;59D;80F;81F;87C;88D;94D / ray + In(3LR)63B;85D T(2;3)shvS25 22F1-2;88E1-4 / ray ( Induced on dppd-ho chromosome. | New order: 21 - 22F|35A - 22F|97A - 61A; 100F - 97A|35A - 60F. / New order: 21 - 22F|(80F - 81F)|87C - 85D|63B - 80F|81F - 85D|63B - 61A; 60F - 59D|88D - 87C|88D - 94D|22F - 59D|94D - 100F. (tentative chromocentral arrangement) #*T(2;3)SM2: Translocation (2;3) Second Multiple cytology: T(2;3)21A;40F;80-81 superimposed on In(2L)22D1- 2;33F5-34A1 + In(2LR)22A3-B1;60B-C + In(2R)42A2-3;58A4-B1; position of breaks in proximal heterochromatin with respect to centromeres not determined. origin: X ray induced in In(2LR)SM1. discoverer: R. F. Grell, 1953. references: Lewis and Mislove, 1953, DIS 27: 58. Mislove and Lewis, 1954, DIS 28: 77. genetics: Variegated for lt. other information: The translocation impairs its general use- fulness as a chromosome 2 balancer; described as SM2 (see Balancers in Special Chromosomes section). # T(2;3)smg: Translocation (2;3) smudge cytology: T(2;3)24D;92A. synonym: T(2;3)T1. references: Robinson and Curtis, 1972, Can. J. Genet. Cytol. 14: 129-37. 1973, Genetica 44: 591-601. genetics: Homozygotes viable and fertile, with abnormal eye ("smudge" effect). Heterozygotes wild type and semisterile (Robinson and Curtis, 1973). In double heterozygotes T(2;3)gls/T(2;3)smg, females are more fertile than males (Robinson and Curtis, 1972). # T(2;3)SMG: Translocation (2;3) Semenova Mglinetz Glotoff origin: / ray induced. references: Semenova, Mglinetz, and Glotoff, 1970, Genetika (Moscow) 6: 165-69. translocation cytology _______________________________ T(2;3)SMG41 27B;92C T(2;3)SMG42 27F;66B T(2;3)SMG43 26E;54D;76C;84F # T(2;3)sna: Translocation (2;3) snail cytology: T(2;3)24B-C;35C-D;41;81. 24C-D to 35B-C inverted. discoverer: Simpson. synonym: RY2. genetics: Mutant for sna. Homozygous lethal. # T(2;3)soDrv: Translocation (2;3) sine-oculis references: Ashburner. genetics: soD revertant. translocation cytology _______________________________ T(2;3)soDrv1 43B1-2;86E14-20 T(2;3)soDrv2 43B3-8;91A3-8 #*T(2;3)sr4.2: Translocation (2;3) stripe cytology: T(2;3)30C;90C-96. origin: X ray induced. discoverer: Alexander. references: 1960, Genetics 45: 1019-22. genetics: Mutant for sr. Homozygous lethal. #*T(2;3)sr100.312 cytology: T(2;3)40-41;90D2-E1. origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42-54. genetics: Mutant for sr. Homozygous lethal. # T(2;3)ssa75 cytology: T(2;3)36D;89C. origin: / ray induced. references: Kaufman, 1978, Genetics 90: 579-96. genetics: Mutant for ssa. #*T(2;3)st100.359: Translocation (2;3) scarlet cytology: T(2;3)21C3-5;73A2-3;98F2-4. new order: 21A - 21C3|73A3 - 98F2|73A2 - 61; 60 - 21C5|98F4 - 100. origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42-54. genetics: Mutant for st. Homozygous lethal. # T(2;3)Su(var)3-5: Translocation (2;3) Suppressor of variegation 3-5 cytology: T(2;3)58B;86B. origin: X ray induced. references: Reuter, Dorn, Wustmann, Friede, and Rauh, 1986, Mol. Gen. Genet. 202: 481-87. genetics: Associated with Su(var)3-5. Recessive semilethal and sterile in both males and females. # T(2;3)Su(z)41: Translocation (2;3) Suppressor of zeste cytology: T(2;3)40-41;80-81. references: Gelbart, 1971, Ph.D. Thesis, Univ. of Wisconsin. genetics: Associated with Su(z). # T(2;3)Su(z)56 cytology: T(2;3)40-41;97F-98B. references: Gelbart, 1971, Ph.D. Thesis, Univ. of Wisconsin. genetics: Associated with Su(z). # T(2;3)sxc2: Translocation (2;3) super sex combs cytology: T(2;3)41C1-2;98C-D;99A-B. new order: 21A - 41C1|99B - 100; 61 - 98C|99A - 98D|41C2 - 60. origin: X ray induced. references: Ingham, 1984, Cell 37: 815-23. genetics: Mutant for sxc. Homozygous lethal and lethal over Df(2R)M41A4. # T(2;3)T origin: X ray induced in stage 7 or stage 14 oocytes of T(2;3)egspy/+ females or T(2;3)apXa/+ females. references: Puro, 1982, DIS 58: 205-08. new genetics of translocation cytology order ( homozygotes _________________________________________________________________________ T(2;3)T1-10 21A-B;34B-C;98F 1 lethal T(2;3)T1-11 39D-F;43E-F;87B 2 viable *T(2;3)T1-12 35B-F;39-41;75C 3 lethal T(2;3)T1-13 30D2-F1;83A2-C1 lethal *T(2;3)T1-16 31F1-32A1;71A1-2 poorly viable *T(2;3)T1-19 22E;89D low viability and fertility over Ubx130 T(2;3)T1-21 41C-42A;45D2-46A1;98F; 4 lethal deficient for 41F-42A? T(2;3)T1-53 | 33D-E;79B;80A; 5 poorly viable duplicated for 79B-80A T(2;3)T1-55 49A2-B1;75B lethal T(2;3)T1-56 32E2-F1;96C2-D1 lethal T(2;3)T1-57 40-41;80-81 lethal T(2;3)T1-58 60F5;64B-C 6 Dp segregant viable and fertile; Df segregant lethal T(2;3)T2-30 41;89A-C ( 1 = 21A|34B - 21B|98F - 61; 60 - 34C|99A - 100. 2 = 21 - 39D|87B - 61; 60 - 43F|39F - 43E|87B - 100. 3 = 21 - 35B|75C - 100; 61 - 75C|(35F - 39)|41 - 60. 4 = 21 - 41C|45D2 - 42A|98F - 100; 61 - 98F|46A1 - 60. 5 = 21 - 33D|79C - 100; 60 - 33E|80A2 - 61. 6 = 21 - 60F5|64B - 61; ?|64C - 100 (terminal attachment of 3L segment to 2R distal to 60F5). | Break in 2 and left break in 3 identical to those in T(2;3)egspy; T(2;3)T1-53 derived from T(2;3)egspy by replace- ment of 61-79A4 by 61-80A1. # T(2;3)Ta1: Translocation (2;3) thickened arista cytology: T(2;3)51E1-2;84B1-2 (Kaufman et al., 1980) or 84C1-2 (Cavener et al., 1986). synonym: T(2;3)TaL. origin: / ray induced. references: Kaufman, 1978, Genetics 90: 579-96. Kaufman, Lewis, and Wakimoto, 1980, Genetics 94: 115-33. Cavener, Corbett, Cox, and Whetten, 1986, EMBO J. 5: 2939-48. Cavener, Otteson, and Kaufman, 1986, Genetics 114: 111-23. genetics: Associated with Ta1. Homozygous lethal. When heterozygous with Ta2, the translocation is viable and shows a transformation of the whole arista and antennal segments four and five into tarsus and, in males, an extreme reduction in number of sex-comb teeth on the first leg (Kaufman et al., 1980). Fails to complement both hat and stk and gives rise to the same lethal "partial eclosion" phenotype (Cavener et al., 1986). molecular biology: Distal (84C1-2) breakpoint at +34 kb; in the 15 kb overlap of Df(3R)Scx2 and Df(3R)dsx2M (Baker and Wolfner, 1988, Genes Dev. 2: 477-89; 0 point = HindIII site in (Tub84D; "+" values to the right, "-" values to the left). # T(2;3)Tabrv100: Translocation (2;3) Transabdominal-reverted cytology: T(2;3)37F-38A;89E + In(3R)89E;90D. origin: X ray induced in In(3R)Tab. references: Celniker and Lewis, 1987, Genes and Development 1: 111-23. genetics: Revertant of dominant Tab phenotype. When hemizy- gous, 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 ven- tral setal band. molecular biology: Lesion associated with the 89E breakpoint lies between 183 and 184 kb on the composite restriction map of the BXC (Bender, Akam, Karch, Beachy, Peifer, Spierer, Lewis, and Hogness, 1983, Science 21: 23-29). # T(2;3)Tabrv185 cytology: T(2;3)50D;89E + In(3R)89E;90D. origin: X ray induced in In(3R)Tab. references: Celnicker and Lewis, 1987, Genes and Development 1: 111-23. genetics: Revertant of dominant Tab phenotype. When hemizy- gous, 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 ven- tral setal band. # T(2;3)TE34Cc: Translocation (2;3) Transposing Element cytology: T(2;3)34D1-2;80-81. origin: / ray induced in TE34Cc. discoverer: Gubb. synonym: T(2;3)TE94V1. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. genetics: Variegates for w. Lethal with l(2)34Da deficiencies. # T(2;3)TE35A origin: / ray induced in TE35A; selected as reversion of z. synonym: T(2;3)TE146Z. translocation cytology discov ( genetics ______________________________________________________________________ T(2;3)TE35A-2a 35B1-2;80 1 wv T(2;3)TE35A-3 35B1-2;86F12-87A2 4 T(2;3)TE35A-3a 35B1-2;80-81(?) + 2 wv T(2;3)25A3-8;67C9 T(2;3)TE35A-4 35B1-2;81 3 wv T(2;3)TE35A-5 35B1-2;80-81 3 wv; noc - vasa T(2;3)TE35A-7 35B1-2;80-81 2 wv T(2;3)TE35A-8 32B2-3;81 + 55;65 + 4 wv In(2L)29D2-3;34D4 | T(2;3)TE35A-25 35B1-2;70B1-2 4 T(2;3)TE35A-26 35B1-2;69F6-7;81;100F / 4 T(2;3)TE35A-28 35B1-2;90C3-6 4 T(2;3)TE35A-58 35B1-2;94A4-5 1 T(2;3)TE35A-200 35B;94A1-2 5 T(2;3)TE35A-202 35B;81 5 T(2;3)TE35A-207 35B;80 + 5 T(2;3)CA47 T(2;3)TE35A-208 35B;80-81 5 T(2;3)TE35A-209 35B;80 5 T(2;3)TE35A-212 35B;67A7-15;80-81 ` 5 T(2;3)TE35A-215 35B;82B 5 T(2;3)TE35A-216 35B;80-81 5 T(2;3)TE35A-218 35B;86E12-13 5 T(2;3)TE35A-221 35B;80-81 5 T(2;3)TE35A-224 35B;67F2-68A1 5 T(2;3)TE35A-227 40;72B-C + In(2L)35B1-2;40 + In(3R)81;88B T(2;3)TE35A-229 35B;80-81 5 T(2;3)TE35A-230 21A4;26C4-D1;68B4-C1 5 + 35B;62A2-3 - ( 1 = Ashburner; 2 = Durrant; 3 = Gubb; 4 = Roote; 5 = Samkange. | New order: 21 - 29D2|34D4 - 29D3|34D4 - 35B2|81 - 65|55 - 60F; 61 - 65|55 - 35B3|81 - 100. / New order: 21 - 35B|69F - 81|69F - 61A; 60 - 35B|81 - 100. ` New order: 21 - 35B|67A - 100; 60 - 35B|67A - 61. - New order: 21 - 21A4|26D1 - 35B|62A3 - 68B4|21A4 - 26C4|68C1 - 100; 60 - 35B|62A2 - 61. # T(2;3)TE35BC origin: / ray induced in TE35BC; selected as wv derivatives. synonym: T(2;3)TE36R. genetics: Variegates for w+ of TE35BC. translocation cytology discoverer ___________________________________________________ T(2;3)TE35BC-1 ( 35C1-3;80 Gubb T(2;3)TE35BC-2 see Tp(2;3)TE35BC-2 T(2;3)TE35BC-3 | 35B5-10;81 Gubb T(2;3)TE35BC-6 35B;80(?) Shelton T(2;3)TE35BC-8 / 35;80 + Shelton In(3L)65;79 T(2;3)TE35BC-9 ` 33B;35B;81 T(2;3)TE35BC-11 33B;80-81 ( Lethal with ck alleles, but not otherwise mutant in region 35. 3L break determined genetically. | wv on 3P2D element. Genetically broken between Adh and l(2)35Bb. Lethal with lethal ck alleles but breakpoint not lethal. 3R break determined genetically. / New order: 21 - 35|80 -100; 61 - 65|79 - 65|79 - 80|35 - 60. Tentative. ` New order: 21 - 35B|81|(33B - 35B)|80 - 61; 60 - 35B|81 - 100. # T(2;3)TE36: see T(2;3)35BC # T(2;3)TE94R: see T(2;3)TE34Cc # T(2;3)TE146Z: see T(2;3)35A # T(2;3)Tlrv3: Translocation (2;3) Toll-revertant cytology: T(2;3)40-41;97D1-2. origin: X ray induced. synonym: T(2;3)TlRXE. references: Anderson, Jurgens, and Nusslein-Volhard, 1985, Cell 42: 779-89. genetics: Revertant of Tl. Heterozygous females viable, fer- tile, and produce dorsalized lethal embryos as maternal effect. # T(2;3)Ubx: Translocation (2;3) Ultrabithorax genetics: Mutant for Ubx. translocation cytology origin discov. ref ( _________________________________________________________________ T(2;3)Ubx1A 41;89E X ray see BXC T(2;3)Ubx1U 31;89E see BXC T(2;3)Ubx4-30 34;89E1-2 X ray 2 T(2;3)Ubx6-26 54E;75C;89E1-2 X ray 2 T(2;3)Ubx105 53C;89E1-2 E.B. Lewis T(2;3)Ubx175 22B1-2;89E 1 T(2;3)Ubx1069 41A;89E X ray R.H. Baker T(2;3)UbxB18 21D1-2;89E EMS Bacher, 65i T(2;3)UbxB36 41F;89E EMS Bacher, 65i T(2;3)UbxD1 41;89E1-2 T(2;3)UbxKM26 59E;75C;89E1-2 X ray 2 T(2;3)UbxKM30 34;89E1-2 X ray 2 T(2;3)UbxR10 | 41;89D-E X ray Ramey T(2;3)UbxR17 | 22B1-2;89E1-2 X ray Ramey T(2;3)UbxR22 | 41;89E X ray Ramey T(2;3)UbxR34 | 41;89E X ray Ramey T(2;3)UbxX-type 52A-C;89E E.B. Lewis ( 1 = Craymer; 2 = Kerridge and Morata, 1982, J. Embryol. Exp. Morphol. 68: 211-34. | Synonym: Cbxrev.R17. # T(2;3)V: Translocation (2;3) Valencia origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. genetics of translocation cytology homozygotes _____________________________________________________________________ T(2;3)V3-2 27C-D;74C-D arched wings; semilethal T(2;3)V4-13 58B-C;78B lethal T(2;3)V8-2 30B;97F-98A lethal T(2;3)V9-1 40-41;62F lethal T(2;3)V9-10 35A;90F lethal T(2;3)V10-7b 56D-E;89D lethal T(2;3)V11-1 49C-D;65F viable, fertile T(2;3)V11-3-3 54C;62A1 lethal T(2;3)V11-3e 46D;63C lethal T(2;3)V11-3g ( 24A-B;53B;81F lethal T(2;3)V12-1-6 55F;62E + In(2L)21F;29B-C lethal T(2;3)V12-1-10 42F-43A;81-82 lethal T(2;3)V12-1-32 59F;79F lethal T(2;3)V12-1-41 22E;91F lethal T(2;3)V12-1b 31D;85D lethal T(2;3)V12-2d | 31F-32A;41;53B;78F;94C T(2;3)V13-1 35B;96E + In(3L)70B;71E-F lethal T(2;3)V13-1b 33B;79F lethal T(2;3)V13-2b 60D;96F + Df(2R)49D-E;50B lethal T(2;3)V13-3 40-41;85F lethal T(2;3)V14 40;62C semilethal T(2;3)V16 60B-C;84A + In(3R)93F;99C partially viable T(2;3)V103 58F;67B4 + In(3R)85A;96E lethal T(2;3)V116 41C;75B lethal ( New order: 21 - 24A|81F - 61; 60F - 53B|24B - 53B|81F - 100. | New order: 21 - 31F|78F - 94C|41 - 53B|94C - 100; 61 - 78F|41 - 32A|53B - 60. # T(2;3)vg: Translocation (2;3) vestigial references: Alexandrov and Alexandrova, 1987, DIS 66: 185-87. phen translocation cytology origin under 25C _____________________________________________________________ T(2;3)vg67d1 49C2-D2;93F-F1 / ray lethal T(2;3)vg76i1 49D2-E1;84E2-3 actinomycin-D + lethal / ray T(2;3)vg78b4 49D2-3;49E7-F1;80C NaF + / ray lethal T(2;3)vg79b3 49C2-3;94A2-3 + / ray lethal Df(2R)49C4;49E2 T(2;3)vg81a 49D2-F1;64B2-12 / ray lethal T(2;3)vg83c 49D2-E;65F6-66A / ray vgnp T(2;3)vg85d2 49D2-E;84F4-6 0.85 MeV vg # T(2;3)VV1: Translocation (2;3) V. Velissariou cytology: T(2;3)27A1-2;85A2-6. origin: X ray induced. discoverer: Velissariou. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. # T(2;3)VV6 cytology: T(2;3)57D;65D. origin: X ray induced. discoverer: Velissariou. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. # T(2;3)VW2: Translocation (2;3) V. Walker cytology: T(2;3)49E-50A4;80C. origin: / ray induced. discoverer: Walker. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissarriou, and Walker, 1981, DIS 56: 186-91. genetics: Minute in phenotype. # T(2;3)Xa: see T(2;3)apXa # T(2;3)Y: Translocation (2;3) Ytterborn origin: X ray induced. references: Ytterborn, 1968, Hereditas 59: 49-62. translocation cytology ________________________ T(2;3)Y1 30;96 T(2;3)Y2 54;98 T(2;3)Y3 57;97 # T(2;3;4)429.18 cytology: T(2;3)49A1-2;50B;66B + T(2;4)29F1-2;101 + In(3R)86B- C;87F1-2 + In(3R)89D6-E2;96A. new order: 21 - 29F1|101; 60 - 50B|49A1 - 29F2|101 - 102; 61A - 66B|50B - 49A2|66B - 86B|87F1 - 86C |87F2 - 89D6|96A - 89E2|96A - 100. origin: X ray induced. discoverer: Gelbart. # T(2;3;4)429.29 cytology: T(2;3;4)28D1-2;31D-E;80F;102E-F. new order: 21 - 28D1|31E - 60; 61 - 80F|28D2 - 31D|102E - 101A; 100 - 80F|102F. origin: X ray induced. discoverer: Gelbart. # T(2;3;4)429.36 cytology: T(2;3)40;65A1-2 + T(3;4)71F-72A;101F. origin: X ray induced. discoverer: Gelbart. #*T(2;3;4)bwR58: Translocation (2;3;4) brown-Rearranged cytology: T(2;3;4)59D;65;101C. new order: 21 - 59D|65 - 61; 60 - 59D|101C - 102; ?|65 - 100. 101A to C lost. origin: X ray induced. discoverer: Slatis. references: 1955, Genetics 40: 5-23. genetics: Associated with bwR58. # T(2;3;4)bwV30k18: Translocation (2;3;4) brown-Variegated origin: X ray induced. discoverer: Van Atta, 30k13. references: 1932, Genetics 17: 637-59. genetics: Variegated for bw. Produces aneuploids that have Minute bristles. # T(2;3;4)C: Translocation (2;3;4) Crossover suppressor origin: X ray induced. discoverer: Roberts. synonym: T(2;3;4)16 - T(2;3;4)36. references: 1972, Genetics 71: 401-15. recombination translocation cytology reduced in ______________________________________________________________ *T(2;3;4)C16 T(2;3)35B;97F + T(2;4)48E;101 2L + 2R *T(2;3;4)C20 T(2;3)40-41;80 + T(3;4)89E;101 3R *T(2;3;4)C21 T(2;3)57C;98A + T(2;4)28C;101 2R + 2L *T(2;3;4)C26 T(2;3)21A;68F + T(3;4)89A;101 2L + 3R *T(2;3;4)C36 T(2;3)27B;88A + T(3;4)64F;101 2L + 3L # T(2;3;4)CA4 cytology: T(2;3;4)50E-F;81;89A;94F;101. new order: 21 - 50E|94F - 89A|50F - 60; 61 - 81|89A - 81|101 - 102; 100 - 94F|101 (tentative). origin: / ray induced. discoverer: Ashburner. references: Ashburner, Aaron, and Tsubota, 1982, Genetics 102: 421-35. genetics: Induced with Df(2L)A400. # T(2;3;4)ci7: Translocation (2;3;4) cubitus interruptus cytology: T(2;3;4)24A1;98A1;101D-F + In(2L)27B;29B. new order: 21 - 24A1|98A1 - 61; 60 - 29B|27B - 29B|27B - 24A1|101F - 102; 100 - 98A1|101D - 101A. origin: X ray induced. synonym: R7(ci). references: Stern and Kodani, 1955, Genetics 40: 343-73. genetics: T(2;3;4)ci7/ci flies show more extreme L4 vein interruptions than ci/ci flies. # T(2;3;4)ci10 cytology: T(2;3;4)48B1;49F-50A1;81F;85F;97F1;101D-F;102C1. Complex. new order: 21 - 48B1|85F - 97F1|102C1 - 102F; 61 - 81F|50A1 - 60; 101A - 101D|81F - 85F|101F - 102C1|48B1 - 49F |97F1 - 100. origin: X ray induced. synonym: R10(ci). references: Stern and Kodani, 1955, Genetics 40: 343-73. genetics: T(2;3;4)ci10/ci flies show less extreme L4 vein interruptions than ci/ci flies. # T(2;3;4)ci+3: Translocation (2;3;4) cubitus interruptus-wild type cytology: T(2;3)21D1;75A1 + T(3;4)67C2;101F1 + Tp(3;4)95D- E;97C2;101F1;102F. new order: 102 - 101F1|67C2 - 75A1|21D1 - 60; 21A - 21D1|75A1 - 95D|97C2 - 100; 101A - 101F1|67C2 - 61; 101A - 101F1|95E - 97C2|102F (tentative). Chromosome 4 believed to be split into two chromatids before breaks induced, with one chromatid attached to 3L at 67C2 and the other carrying an insertion of 95E-97C2 and a deletion of most of 4R (Stern et al., 1946). origin: X ray induced. synonym: R3(+); T(2;3;4)+3. references: Stern, MacKnight, and Kodani, 1946, Genetics 31: 598-619. Stern and Kodani, 1955, Genetics 40: 343-73. genetics: T(2;3;4)ci+3/ci flies show L4 vein interruptions, whereas ci+3/ci flies are wild type. # T(2;3;4)ci+14 cytology: T(2;3;4)60B;99B1;101F. Complex. new order: 21 - 60B|99B1 - 100; 61 - 99B1|101F - 102; 101A - 101F|60B - 60F. origin: X ray induced. synonym: R14(+). references: Stern and Kodani, 1955, Genetics 40: 343-73. genetics: T(2;3;4)ci+14/ci flies show L4 vein interruptions, whereas ci+14/ci flies are wild type. # T(2;3;4)dpp9: Translocation (2;3;4) decapentaplegic cytology: T(2;3)22F2-23A1;41A;64F + T(2;3;4)57E-F;80B;101F. new order: 21A - 22F2|41A - 57E|80B - 100; 102F - 101F|80B - 64F|41A - 23A1|64F - 61A; 60F - 57F|101F - 101A (tentative). origin: X ray induced. discoverer: Spenser. references: Gelbart. genetics: d-III mutant. # T(2;3;4)dpp81 cytology: T(2;3)22F1-2;80 + T(2;4)30C;101. origin: / ray induced. discoverer: Segal. references: Gelbart. genetics: d-V mutant. # T(2;3;4)iab4302: Translocation (2;3;4) infraabdominal4 cytology: T(2;3;4)60D;81;89E;100F;101. Complex. origin: X ray induced. discoverer: R.H. Baker. synonym: iab431616.302. genetics: Mutant for iab4. molecular biology: 89E breakpoint 83-86.5 kb distal to the right breakpoint of In(3R)Cbxrv1. # T(2;4)429 - T(2;4)434 origin: X ray induced. discoverer: Gelbart. translocation cytology _______________________________ T(2;4)429.73 see T(2;4)DTD13 T(2;4)429.90 see T(2;4)DTD15 T(2;4)432.37 28A;101 T(2;4)432.64 35E;101 T(2;4)434.06 26A1-2;101A T(2;4)434.33 see T(2;4)DTD37 T(2;4)434.36 see T(2;4)DTD38 T(2;4)434.42 see T(2;4)DTD39 T(2;4)434.53 see T(2;4)DTD40 T(2;4)434.119 32A1-2;102E-F # T(2;4)a cytology: T(2;4)50B2-3;102E (Lewis). origin: X ray induced. discoverer: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1931, Genetics 16: 629-58. genetics: Homozygous lethal. Fly hyperploid for 4P2RD element rarely survives and is sterile. # T(2;4)A: Translocation (2;4) from Austin origin: X ray induced. genetics of translocation cytology ( ref | homozygote ______________________________________________________ *T(2;4)A6 / 57F2-3 2, 3 viable, sterile *T(2;4)A8 ` 26F4-27A1 2, 3 viable, fertile *T(2;4)A23 58F 3 viable, sterile *T(2;4)A27 40D1-F1 1, 2, 3 lethal *T(2;4)A29 47A4-5 2, 3 lethal *T(2;4)A30 53B2-C1 1, 2, 3 viable, fertile *T(2;4)A34 - 56A6-7 1, 2, 3 viable *T(2;4)A35 26E 3 viable *T(2;4)A40 49F3-50A1 1, 2, 3 viable, fertile *T(2;4)A43 22C 2, 3 viable, fertile *T(2;4)A45 36D 3 lethal viable, fertile *T(2;4)A52 36B 3 viable, fertile T(2;4)A53 36E1-3 1, 2, 3 viable, fertile ( Breakpoint in chromosome 4 not determined. | 1 = Burdette, 1940, Texas Univ. Publ. 4032: 157-63; 2 = Patterson, Brown, and Stone, 1940, Texas Univ. Publ. 4032: 167-89; 3 = Patterson, Stone, Bedichek, and Suche, 1934, Am. Nat. 68: 359-69. / Fly hyperploid for the 4P2RD element viable and fertile. ` Fly hyperploid for the 4P2LD element viable and fertile. - Either acts as or carries a dominant suppressor of Pu (Oliver, 1943, Anat. Rec. 87: 461). 4P2LD element not recoverable in hyperploid; therefore translocation probably more complex than given. # T(2;4)astv: Translocation (2;4) asteroid-variegated cytology: T(2;4)21E2-3;101. origin: X ray induced. discoverer: E.B. Lewis, 1940. references: 1945, Genetics 30: 137-166. genetics: Variegates for S, ast, and ci. Homozygous lethal. Fly with 2P4D element in place of one chromosome 2 survives and has extremely rough eyes. 2P4D is deficient for l(2)gl and net and presumably for al, ex, and ds. Fly hyperploid for complementary 4P2LD also survives. # T(2;4)b cytology: T(2;4)25E;102C15-D1 (Schultz and Lewis). Metaphase chromosome 4 twice normal size. origin: X ray induced. discoverer: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1931, Genetics 16: 629-58. genetics: ci not affected. Homozygous viable and fertile. Fly hyperploid for 4P2LD element survives; short and thick with flattened abdomen, bulging eyes, and curved wings; both sexes sterile. Duplicated for M(2)25A and dp but not cl, ey, or sv (Morgan, 1946, DIS 20: 88). # T(2;4)BIII17 cytology: T(2;4)40-41;101F. references: Yamamoto, 1987, DIS 66: 192-93. #*T(2;4)bwR25: Translocation (2;4) brown-Rearranged cytology: T(2;4)59D;101E. origin: X-ray-induced derivative of bw. discoverer: Slatis. references: 1955, Genetics 40: 5-23. genetics: Associated with bwR25. #*T(2;4)c cytology: Metaphase chromosome 4 about twice normal size. origin: X ray induced. discoverer: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1961, Genetics 16: 629-58. genetics: Homozygote nearly lethal; wings do not expand; fly dies early. Break in 2L between dp and b, close to dp. Male hyperploid for 4P2LD element poorly viable and sterile. No variegation for ci+ (Stern). # T(2;4)C: Translocation (2;4) Crossover suppressor origin: X ray induced. discoverer: Roberts. synonym: T(2;4)2 - T(2;4)90. references: 1972, Genetics 71: 401-15. Xover translocation cytology reduced in _____________________________________ *T(2;4)C2 60A;101 2R *T(2;4)C4 53E;101 2R *T(2;4)C7 57E;101 2R *T(2;4)C8 48C;101 2R *T(2;4)C9 33C;101 2L *T(2;4)C13 53E;101 2R *T(2;4)C14 55F;101 2R *T(2;4)C15 29B;101 2L *T(2;4)C18 34B;101 2L *T(2;4)C19 26C;101 2L *T(2;4)C22 33A;101 2L *T(2;4)C24 35B;101 2L *T(2;4)C25 30B;101 2L *T(2;4)C29 34E;101 2L *T(2;4)C31 30E;101 2L *T(2;4)C32 22A;101 2L *T(2;4)C33 30B;101 2L *T(2;4)C37 35F;101 2L *T(2;4)C39 60A;101 2R *T(2;4)C58 49A;101 2R *T(2;4)C81 60E;101 2R *T(2;4)C84 24F;101 2L *T(2;4)C90 32A;101 2L # T(2;4)CA36 cytology: T(2;4)48C1-2;102A-B. origin: / ray induced. discoverer: Ashburner. references: Gubb, Shelton, Roote, McGill, and Ashburner, 1984, Chromosoma 91: 54-64. other information: Associated with Df(2L)TE35BC-29. # T(2;4)ci: Translocation (2;4) cubitus interruptus origin: X ray induced. synonym: RX(ci). translocation cytology ref ( genetics | ______________________________________________________ T(2;4)ci2 44C3;102C3 2 1 (females); 2 (males) T(2;4)ci3 52E1;101 2 1 T(2;4)ci6 47D3;102D3 2 2 T(2;4)ci7 see T(2;3;4)ci7 T(2;4)ci9 38B2;101 2 1 T(2;4)ci16 45E1;102D3 2 2 T(2;4)ci30 40-41;101 2 1 T(2;4)ci33 48C-D;101F 2 1 T(2;4)ci36 47A1;102C1 1, 2 2 T(2;4)ci42 40-41;101 2 1 T(2;4)ci44 40-41;101 2 1 T(2;4)ci45 58D;102D-E 1, 2 2 T(2;4)ci53 47B5;101 2 1 ( 1 = Altorfer, 1967, Genetics 55: 755-67; 2 = Stern and Kodani, 1955, Genetics 40: 343-73. | 1 = T(2;4)ci/ci flies show more extreme L4 vein interrup- tions than ci/ci flies; 2 = T(2;4)ci/ci flies show less extreme L4 vein interruptions than ci/ci flies. # T(2;4)ci+: Translocation (2;4) cubitus interruptus-wild type origin: X ray induced. synonym: RX(+). references: Stern and Kodani, 1955, Genetics 40: 343-73. genetics: T(2;4)ci+/ci flies show L4 vein interruptions, whereas ci+/ci flies are wild type. translocation cytology _____________________________________________ T(2;4)ci+6 59D;101 T(2;4)ci+10 31F1;102B1 (complex) T(2;4)ci+11 47C;102B1 T(2;4)ci+18 57F1;101F T(2;4)ci+20 55A;101 T(2;4)ci+21 60E1;101F # T(2;4)d cytology: T(2;4)55E-F (Lewis, 1956, DIS 30: 130); breakpoint in chromosome 4 not determined. origin: X ray induced. discoverer: Dobzhansky, 1929. references: 1930, Biol. Zentr. 50: 671-85. 1931, Genetics 16: 629-58. genetics: Homozygote nearly lethal; fly is short lived and has inflated wings. No viable aneuploid product; therefore, prob- ably more complex than indicated. # T(2;4)dpp71: Translocation (2;4) decapentaplegic cytology: T(2;4)22F1-2;101. origin: / ray induced. discoverer: Segal. references: Gelbart. genetics: d-III mutant. # T(2;4)dpp73 cytology: T(2;4)22F1-2;57A;101F. new order: 21A - 22F1|101F - 101A; 60F - 57A|22F2 - 57A|101F - 102F. origin: / ray induced. discoverer: Segal. references: Gelbart. genetics: d-III mutant. # T(2;4)DTD: Translocation (2;4) Disrupter of Transvection at Decapentaplegic origin: X ray induced; 15 induced in dpp4, 22 in Dp(1;2)w+70h, dppho2, 37-40 in dppho2, and 103 and 112 in dppho2 TE23C- D[w+]. genetics: Disrupts transvection at dpp. translocation cytology ref ( ______________________________________ T(2;4)DTD13 24A1-2;101A-D 2 T(2;4)DTD15 22F3-4;102F 2 T(2;4)DTD22 35E1-2;101 3 T(2;4)DTD22.12 25D-E;102D-E 1 T(2;4)DTD37 28D;101A 2 T(2;4)DTD38 29B;32A;101A 2 T(2;4)DTD39 24C;102B 2 T(2;4)DTD40 25C;102B 2 T(2;4)DTD103 35D-E;102D-E 3 T(2;4)DTD112 23C-D;102E-F 3 ( 1 = Gelbart. 2 = Gelbart, 1982, Proc. Nat. Acad. Sci. USA 79: 2636-40; 3 = Smolik-Utlaut and Gelbart, 1987, Genetics 116: 285-98. # T(2;4)GT6 cytology: T(2;4)34F3;101-102. origin: / rays. discoverer: Durrant. genetics: Mutant for wb - l(2)34Fc. # T(2;4)K references: Yamamoto, 1987, DIS 66: 192-93. translocation cytology comments __________________________________________________ T(2;4)K10 57F3-6;101F T(2;4)K12 49B;101F *T(2;4)K13 25A3-4;101F T(2;4)K22 56F12-15;101F eye color brownish T(2;4)K44 T(2;4)K53 53C;101F T(2;4)K55 27E;101F T(2;4)K86 42A;101F homozygous viable T(2;4)K89 52F7-9;101F homozygous viable T(2;4)K92 47E;101F T(2;4)K109 50C1-2;101F T(2;4)K419 35F;101F # T(2;4)ltm3: Translocation (2;4) light-mottled 3 cytology: T(2;3)40;60D;102F (Craymer). synonym: In(2LR)ltm3. references: Hessler, 1957, Genetics 43: 495-503. genetics: Variegated for lt. # T(2;4)shvS9: Translocation (2;4) shortvein of Segal cytology: T(2;4)22F1-2;101. origin: / ray induced. references: Segal and Gelbart, 1985, Genetics 109: 119-43. genetics: Associated with shv. Lethal over shv and other lethal dpp alleles. # T(2;4)shvS14 cytology: T(2;4)22F1-2;101-102. origin: / ray induced. references: Segal and Gelbart, 1985, Genetics 109: 119-43. genetics: Associated with shv. Lethal over shv and other lethal dpp alleles. # T(2;4)TE35A-11 cytology: T(2;4)35B;101F. origin: / ray induced in TE35A. discoverer: Durrant. synonym: T(2;4)TE146Z. genetics: Variegates for w+. # T(2;4)TE35A-50 cytology: T(2;4)35B1-2;101-102. origin: / ray induced in TE35A. discoverer: Roote. synonym: T(2;4)TE146Z. genetics: Red-eyed on z w background. # T(2;4)TE35A-101 cytology: T(2;4)35B;101-102. origin: / ray induced. synonym: T(2;4)TE146Z. # T(2;4)TE35A-214 cytology: T(2;4)35A-B;102C. origin: / ray induced in TE35A. discoverer: Samkange. synonym: T(2;4)TE146Z. # T(2;4)V24: Translocation (2;4) Valencia cytology: T(2;4)60A-B;102D-E. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. genetics: Homozygous lethal. # T(2;4)Y origin: X ray induced. references: Yamamoto, 1987, DIS 66: 192-93. translocation cytology comments _________________________________________________________ T(2;4)Y2 35D3-4;101F *T(2;4)Y7 50C14-D1;102C-D wing margin depleted *T(2;4)Y22 41;101F T(2;4)Y34 36C-D;101F T(2;4)Y40 56B-C;101F T(2;4)Y47 31D-E;101F *T(2;4)Y64 35C;101F T(2;4)Y76 40-41;101F homozygous viable T(2;4)Y86 21E1-2;101F T(2;4)Y92 57B4-6;101F *T(2;4)Y100 21D;101F T(2;4)Y106 55A;101F homozygous viable T(2;4)Y109 40-41;59B;101F *T(2;4)Y141 40-41;101F T(2;4)Y142 52E;102C homozygous viable T(2;4)Y164 33A;101F T(2;4)Y185 52D;101F T(2;4)Y209 36C-D;101F homozygous viable T(2;4)Y220 56F6-8;101F T(2;4)Y231 52F;102D T(2;4)Y241 54D-E;101F T(2;4)Y296 T(2;4)Y308 49F10-15;101F *T(2;4)Y316 *T(2;4)Y318 40-41;101F T(2;4)Y325 34E-F;101F homozygous viable T(2;4)Y344 59F;101F T(2;4)Y375 60F5;101F T(2;4)Y376 33C;101F T(2;4)Y423-A 21B3-5;101F T(2;4)Y465 52D9;101F T(2;4)Y476 29D;101F T(2;4)Y492 30A7-9;56F8-9;101F T(2;4)Y496 22A1-2;101F T(2;4)Y517 54F;101F