# T(3;4)85C cytology: T(3;4)85C; breakpoint in chromosome 4 not determined. discoverer: E.B. Lewis. references: Pipkin, 1959, Texas Univ. Publ. 5914: 69-88. # T(3;4)86D cytology: T(3;4)86D2-3;101F. origin: Neutron induced in bx34e e4. discoverer: E.B. Lewis. references: Grell, 1959, Genetics 44: 421-35. 1959, Genetics 44: 911-22. Grell and Day, 1970, Chromosoma 31: 434. genetics: Homozygous viable and fertile. T(3;4)86D/ci has ci effect, is enhanced by low temperature, and tends to be suppressed by extra Y chromosome. Venation of homozygote and haplo-4 is ci+. # T(3;4)88B cytology: T(3;4)88B; breakpoint in 4 not determined. origin: X ray induced in Ubx. discoverer: E.B. Lewis. references: Grell, 1959, Genetics 44: 421-35. genetics: Homozygous lethal. Has no position effect on ci. # T(3;4)89E cytology: T(3;4)89E2-3;101F. origin: X ray induced in ss bx Su(ss)2. discoverer: E.B. Lewis. references: Grell, 1959, Genetics 44: 911-22. genetics: Associated with bxd101. Homozygous lethal. T(3;4)89E/ci has a ci effect, is enhanced by low temperature, and tends to be suppressed by extra Y chromosome. # T(3;4)104: see Tp(4;3)f # T(3;4)429.10 cytology: T(3;4)99B1-2;102D + In(3R)81F;86B-C. origin: X ray induced. discoverer: Gelbart. #*T(3;4)684 cytology: T(3;4)67;101; breakpoints roughly estimated from fig- ure of Dubinin and Sidorov (1935). origin: X ray induced. discoverer: Dubinin and Sidorov. references: 1934, Biol. Zh. (Moscow) 3: 307-31. 1935, Biol. Zh. (Moscow) 4: 555-68 (fig.). genetics: Position effects on both h and ci. # T(3;4)a cytology: Chromosome 4 increased to about one-half length of 3L in metaphase figures. origin: X ray induced. discoverer: Dobzhansky, 29h. references: 1929, Biol. Zentr. 49: 408-19. 1929, Proc. Nat. Acad. Sci. USA 15: 633-38. 1930, Genetics 15: 347-99. genetics: Homozygous lethal. Break in 3L between D and th. # T(3;4)A: Translocation (3;4) from Austin origin: X ray induced. genetics of translocation cytology ref ( homozygote __________________________________________________________________ *T(3;4)A1 89A6-B1;102B 3, 5 viable and fertile (Patterson et al., 1934); lethal (CP552) T(3;4)A2 | 94A3-4;101F 1, 3, 5 viable and fertile (Brown) *T(3;4)A3 3, 5 lethal; 3R break between e and ca *T(3;4)A4 80-81;101 3, 5 lethal *T(3;4)A5 92A5-6 2, 5 lethal *T(3;4)A8 75B4-5;102D1-3 1, 2, 3, 5 viable and fertile (Brown) *T(3;4)A9 87E3-F1;102F 1, 3, 5 viable and fertile T(3;4)A12 / 73C1-2;102C 2, 3, 5, 6 poorly viable and fertile T(3;4)A13 / 67E3-4;102D-E 3, 4, 5, 6 lethal *T(3;4)A14 80;101 3, 5 *T(3;4)A20 89A;101F 3, 5 lethal *T(3;4)A22 61E-F;102B-C 3, 5 lethal; 3L broken to left of ru *T(3;4)A23 66D5-E1;101F 3, 5 lethal in male; viable in female *T(3;4)A24 99;102B-C 3, 5 viable and fertile *T(3;4)A27 82B3-C1;101A-D 1, 2, 3, 5 viable and fertile T(3;4)A28 94D3-4;102 3, 5, 6 viable and fertile (E.B. Lewis) *T(3;4)A30 | 96E5-F1;102B-C 3, 5, 6 lethal *T(3;4)A31 80;101 1, 2, 3, 5 viable and fertile *T(3;4)A34 61F;101F 3, 5 lethal; 3L broken to left of ru *T(3;4)A36 80B3-C1;102E 1, 2, 3, 5 viable and fertile (Brown) *T(3;4)A37 86E5-6;101F 3, 5 lethal *T(3;4)A39 94B4-C1;101F 2, 3, 5 lethal *T(3;4)A43 3, 5 lethal; 3R broken near sr *T(3;4)A44 ` 76;99;102D-F 3, 5 lethal *T(3;4)A45 80;101 3, 5 viable but sterile *T(3;4)A52 65D3-F2 3, 5 viable and fertile *T(3;4)A56 76E2-F3;101F 3, 5 lethal *T(3;4)A60 see *T(3;4)A3 ( 1 = Brown, 1940, Texas Univ. Publ. 4032: 11-64; 2 = Burdette, 1940, Texas Univ. Publ. 4032: 157-63; 3 = Painter, 1935, Genetics 10: 301-26; 4 = Patterson, Brown, and Stone, 1940, Texas Univ. Publ. 4032: 167-89; 5 = Patterson, Stone, Bedi- chek, and Suche, 1934, Am. Nat. 68: 359-69. 6 = Pipkin, 1959, Texas Univ. Publ. 5914: 60-88. | Fly hyperploid for 4P3RD element survives. / Fly hyperploid for 4P3LD element survives. ` New order: 61 - 76|102D - 101; 100 - 99|76 - 99|102F. # T(3;4)Antprv2: Translocation (3;4) Antennapedia-revertant cytology: T(3;4)84B1-3;102F. origin: X ray induced in AntpNs. synonym: T(3;4)AntpNs+R2. references: Duncan and Kaufman, 1975, Genetics 80: 733-52. Lewis, Kaufman, Denell, and Tallerico, 1980, Genetics 95: 367-81. genetics: Revertant of AntpNs. Lethal homozygous and when heterozygous with ANTC mutants. #*T(3;4)b cytology: Chromosome 4 increased to one-half the length of 3L in metaphase figures. origin: X ray induced. discoverer: Dobzhanksy, 28h. references: 1929, Biol. Zentr. 49: 408-19. 1929, Proc. Nat. Acad. Sci. USA 15: 633-38. 1930, Genetics 15: 347-99. genetics: Breakpoint in 3L near th. Crossing over markedly lowered near th and somewhat so at 3L tip. # T(3;4)BII8 cytology: T(3;4)77A;101F. references: Yamamoto, 1987, DIS 66: 192-93. # T(3;4)BII13 cytology: T(3;4)93E;101F. references: Yamamoto, 1987, DIS 66: 192-93. # T(3;4)BTD1: Translocation (3;4) Bithorax Tranvection Disrupter cytology: T(3;4)87A;102D origin: / ray induced. references: Smolik-Utlaut and Gelbart, Genetics 116: 285-98. # T(3;4)bxd101: Translocation (3;4) bithoraxoid cytology: T(3;4)89E;101F. origin: X ray induced. discoverer: E.B. Lewis. references: 1981, Developmental Biology Using Purified Genes (Brown and Fox, eds.). Academic Press, New York, Vol. 23, pp. 189-208. genetics: Mutant for bxd. # T(3;4)c cytology: T(3;4)86B-C;101F (Lewis, 1951, DIS 25: 108-9). origin: X ray induced. discoverer: Dobzhansky, 28h. references: 1929, Biol. Zentr. 49: 408-19. 1929, Proc. Nat. Acad. Sci. USA 15: 633-38. 1930, Genetics 15: 347-99. genetics: Homozygous viable and fertile. ci not affected. Crossing over much reduced near breakpoint in heterozygote and even more reduced in homozygote in some regions (Beadle, 1932, Proc. Nat. Acad. Sci. USA 18: 160-65). # T(3;4)C: Translocation (3;4) Crossover suppressor origin: X ray induced. discoverer: Roberts. synonym: T(3;4)1 - T(3;4)90. Xover translocation cytology ref ( reduced in _______________________________________________ *T(3;4)C1 92A;101 2 3R *T(3;4)C3 94C;101 2 3R *T(3;4)C5 69B;101 2 3L *T(3;4)C6 92B;101 2 3R *T(3;4)C10 | 100B;101 1, 2, 3 3R *T(3;4)C11 89A;101 2 3R *T(3;4)C12 66B;101 2 3L *T(3;4)C17 98A;101 2 3R *T(3;4)C23 86E;101 2 3R *T(3;4)C27 61A;101 2 3L *T(3;4)C28 93D;101 2 3R *T(3;4)C40 61F;101 2 3L *T(3;4)C44 96F;101 2 3R *T(3;4)C46 67F;101 2 3L *T(3;4)C49 100B;101 2 3R *T(3;4)C51 92D;102A 2 3R *T(3;4)C61 62E;101 2 3L *T(3;4)C80 66A;101 2 3L *T(3;4)C82 94A;101 2 3R *T(3;4)C83 97D;101C 2, 3 3R *T(3;4)C85 61F;101 2 3L *T(3;4)C87 91C;101 2 3R ( 1 = Roberts, 1972, DIS 48: 92; 2 = Roberts, 1972, Genetics 71: 401-15; 3 = Roberts, 1972, Genetics 72: 607-14. | Homozygous lethal. # T(3;4)CA28 cytology: T(3;4)83D;102C. origin: / ray induced with T(2;3)TE35BC-6. discoverer: Ashburner. # T(3;4)ci: Translocation (3;4) cubitus interruptus origin: X ray induced. synonym: RX(ci). genetics: T(3;4)ci/ci flies show more extreme vein interruption than ci/ci flies in all cases except in females of T(3;4)ci4 and T(3;4)ci17 and males of T(3;4)ci35 in which the situation is reversed. translocation cytology ref ( ____________________________________ T(3;4)ci4 80-81;101 1, 2 T(3;4)ci5 69E2;102B1 1, 2 T(3;4)ci8 69F2;101 1, 2 T(3;4)ci13 80-81;102E1 2 T(3;4)ci15 100A2;102C1 2 T(3;4)ci17 67E1;102C1 1, 2 T(3;4)ci18 86C8;102B1 2 T(3;4)ci19 97D9;101 2 T(3;4)ci22 8C1;102B1 1, 2 T(3;4)ci23 92E2;101F 1, 2 T(3;4)ci25 81F;101 1, 2 T(3;4)ci26 90B1;102D1 2 T(3;4)ci27 84B3-4;102F1 2 T(3;4)ci28 80-81;101 1, 2 T(3;4)ci29 94B2;101 1, 2 T(3;4)ci31 75A1;101 1, 2 T(3;4)ci32 2E2;102A 1, 2 T(3;4)ci34 80;101 2 T(3;4)ci35 79F;101 1, 2 T(3;4)ci37 80-81;101 2 T(3;4)ci39 80-81;102D1 2 T(3;4)ci40 | 94A1;102F2 2 T(3;4)ci41 98C-D;102C1 1, 2 T(3;4)ci43 86A1;102F 2 T(3;4)ci48 80-81;101 1, 2 T(3;4)ci52 / 76A1;101F 2 T(3;4)ci54 87F;101F 2 T(3;4)ci55 65F2;101F 2 ( 1 = Altorfer, 1967, Genetics 55: 755-67; 2 = Stern and Kodani, 1955, Genetics 40: 343-73. | Originally a T(Y;3;4) but Y component lost before testing for ci phenotype (Stern and Kodani, 1955). / Altorfer (1967) claims linkage to chromosome 3 lost later. # T(3;4)ci+: Translocation (3;4) cubitus interruptus-wild type origin: X ray induced. synonym: RX(+). references: Stern and Kodani, 1955, Genetics 40: 343-73. genetics: T(3;4)ci+/ci flies show L4 vein interruptions, whereas ci+/ci flies are wild type. translocation cytology ___________________________________ T(3;4)ci+2 ( 82D;101A-D T(3;4)ci+5 96E1;101F T(3;4)ci+8 96F6;102A T(3;4)ci+9 97C1;101F T(3;4)ci+12 ( 98F1;101 T(3;4)ci+13 65D1;102A T(3;4)ci+16 90E1;101F T(3;4)ci+19 62D3;102B1 ( Involves break between ci and the centromere (Stern, MacK- night, and Kodani, 1946, Genetics 31: 598-619). #*T(3;4)d cytology: Metaphase figures show barely detectable increase in size of chromosome 4. origin: X ray induced. discoverer: Dobzhansky, 28h. references: 1929, Biol. Zentr. 49: 408-19. 1929, Proc. Nat. Acad. Sci. USA 15: 633-38. 1930, Genetics 15: 347-99. genetics: Homozygous lethal. ci not affected (Stern). Break- point in 3R between ca and M(3)99E and in 4 to the left of M(4) and ey. Apparently, 3P4D element can substitute for a normal 3, producing Minute flies. Hyperploids for 4P3D ele- ment probably also survive. # T(3;4)Dl7P: Translocation (3;4) Delta-7 of Panshin origin: X ray induced. discoverer: Panshin. references: 1935, Dolk. Akad. Nauk SSSR 4: 85-88. genetics: Chromosome 3 broken to the right of cu. Mutant for Dl; position effect that weakens dominance of cu+. # T(3;4)e cytology: T(3;4)79E;102F (Lewis, 1956, DIS 30: 130). origin: X ray induced. discoverer: Dobzhansky, 28h. references: 1929, Biol. Zentr. 49: 408-19. 1929, Proc. Nat. Acad. Sci. USA 15: 633-38. 1930, Genetics 15: 347-99. genetics: Homozygous semilethal and female sterile. ci not affected (Stern). Crossing over normal in heterozygote except near p. # T(3;4)E(spl)rv: Translocation (3;4) Enhancer of split-reverted origin: X ray induced. genetics: Loss of function mutants. Lethal as homo- and hemiz- ygotes. Variable neural hypoplasia in deficiency heterozy- gotes. translocation cytology discoverer ref ( molecular biology | __________________________________________________________________________ T(3;4)E(spl)rv4 / 96F8-9;100F5;100B-D Bremer 1, 2, 3 proximal to -15 kb T(3;4)E(spl)rv6 ` 96F12-14;102E-F Knust, 1, 2, 3 -5 kb Ziemer T(3;4)E(spl)rv7 96F7-11;102B-C Tietz 2, 3 +2 kb to +5 kb ( 1 = Knust, Bremer, Vassin, Ziemer, Tepass, and Campos- Ortega, 1987, Dev. Biol. 122: 262-73; 2 = Knust, Tietze, and Campos-Ortega, 1987, EMBO J. 6: 4113-23; 3 = Ziemer, Andreas, Tietze, Knust, and Campos-Ortega, 1988, Genetics 119: 63-74. | Position of 3R breakpoint. Origin (coordinate 0) is the first EcoR1 site to right of the genomic fragment homologous to the cDNA clone 126 D12 used to start the E(spl) chromo- somal walk, "+" values to the right, "-" values to the left (Knust et al., 1987b). / 70% lethality with E(spl). 40-50% spl wing in heterozygotes over wild-type. ` 60% lethality with E(spl). No spl wings in heterozygotes over wild type. #*T(3;4)H: Translocation (3;4) from Howard University origin: X ray induced. discoverer: Pipkin. references: 1959, Texas Univ. Publ. 5914: 69-88. translocation cytology of 3 ______________________________________ *T(3;4)H1 80-81 *T(3;4)H3 80-81 *T(3;4)H5 ( 96E *T(3;4)H6 ( 98A *T(3;4)H7 66C ( Fly hyperploid for 4P3RD survives. # T(3;4)iab4125: Translocation (3;4) infraabdominal4 cytology: T(3;4)89E;101D. origin: X ray induced in Mcp. discoverer: R.H. Baker. references: Karch, Weiffenbach, Peifer, Bender, Duncan, Cel- niker, Crosby, and Lewis, 1985, Cell 43: 81-96. genetics: Associated with iab4. Partial revertant of Mcp. molecular biology: 89E breakpoint 81-83 kb distal to the right breakpoint of In(3R)Cbxrv1. # T(3;4)K references: Yamamoto, 1987, DIS 66: 192-93. translocation cytology comments ____________________________________________ T(3;4)K5 T(3;4)K11 homozygous viable *T(3;4)K19 T(3;4)K19 94D;101F *T(3;4)K30 T(3;4)K30 T(3;4)K31 79F;101F T(3;4)K85 64C;101F T(3;4)K87 87D;101F T(3;4)K95 T(3;4)K104 homozygous viable T(3;4)K108 T(3;4)K116 homozygous viable T(3;4)K117 homozygous viable #*T(3;4)K: Translocation (3;4) of Kirssanov origin: X ray induced. discoverer: Kirssanov. references: 1933, Biol. Zh. (Moscow) 2: 447-50. # T(3;4)l-18: Translocation (3;4) lethal origin: X ray induced. discoverer: Gloor and Green, 1957. genetics: Variegates for ci. Mutant for l(4)102ABe. # T(3;4)Mg198 Translocation (3;4) Mglinetz cytology: T(3;4)93E;101-102. origin: 32P feeding. references: Mglinetz, 1968, Genetika (Moscow) 4(8): 81-86. # T(3;4)p42: Translocation (3;4) pink cytology: T(3;4)85A;101D. origin: X ray induced. references: Kemphues, Raff, and Kaufman, 1983, Genetics 105: 345-56. genetics: Mutant for p. # T(3;4)P86: Translocation (3;4) from Pasadena cytology: T(3;4)88B-C;101 (Lewis). origin: X ray induced. discoverer: E.B. Lewis. # T(3;4)ryps1149: Translocation (3;4) rosy-purine-sensitive cytology: T(3;4)87B;101F. 87B-D thought to be inverted [In(3R)81;87B-D] so that 87D placed next to heterochromatin (Rushlow and Chovnick, 1984). origin: / ray induced in ry+11-bearing third chromosome. references: Rushlow and Chovnick, 1984, Genetics 108: 589-602. Rushlow, Bender, and Chovnick, 1984, Genetics 108: 603-15. Clark and Chovnick, 1986, Genetics 114: 819-40. genetics: Homozygous lethal. Variegates for ry with respect to XDH content of Malpighian tubules (Rushlow et al., 1984); also variegates for snk (Clark and Chovnick, 1986). Purine- sensitive in heterozygotes with ry2 or ry41 (Rushlow and Chov- nick, 1984). Has break in pic locus and is associated with pic- phenotype (Clark and Chovnick, 1986). molecular biology: 3R breakpoint between 160 and 150 kb proxi- mal to the origin of the walk, which is 6.5 kb distal to the proximal breakpoint of In(3R)Cbxrv1; approximately 15 kb distal to ry (Rushlow et al., 1984). # T(3;4)SS406 cytology: T(3;4)65B;101. origin: X ray induced. discoverer: Smith. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. # T(3;4)UbxA Translocation (3;4) Ultrabithorax cytology: T(3;4)67;69;70;84;85;87F;88F;89E;100B;102E-F. Extremely complex; breakpoints identified tentatively (E.B. Lewis). origin: X ray induced. discoverer: Schalet, 1959. synonym: In(3LR)UbxA. references: 1960, DIS 34: 53, 55. Craymer, 1980, DIS 55: 197-200. genetics: Associated with UbxA. Homozygous lethal. # T(3;4)UbxR40 cytology: T(3;4)89E;101. origin: X ray induced. discoverer: Ramey. synonym: CbxrevR17.40R. genetics: Associated with UbxR40. # T(3;4)Y references: Yamamoto, 1987, DIS 66: 192-93. translocation cytology comments _________________________________________________________ T(3;4)Y9 65B4:101F T(3;4)Y13 80-81;101F T(3;4)Y25 + In(3R) 90C:98C;101F T(3;4)Y37 80-81;101 T(3;4)Y57 75F;102C *T(3;4)Y61 92A;101F T(3;4)Y63 80-81;101F homozygous viable T(3;4)Y71 81F;101F T(3;4)Y78 100F;102C14 T(3;4)Y81 64E;101F eye deformed T(3;4)Y104 96A1-4;101F T(3;4)Y121 80-81;101 *T(3;4)Y140 96A20-25;101F T(3;4)Y144 88C;101F T(3;4)Y151 78B;101F T(3;4)Y154 72C;101F T(3;4)Y161 99E;101F T(3;4)Y168 76B1;102D T(3;4)Y175 91D;101F T(3;4)Y177 77B;101F *T(3;4)Y183 68D;101F T(3;4)Y210 67E;101F homozygous viable T(3;4)Y226 63D;101F homozygous viable T(3;4)Y249 80-81;101F T(3;4)Y252 80-81;101F homozygous viable T(3;4)Y255 94B;101F T(3;4)Y262 71F;101F homozygous viable T(3;4)Y285 96D-E;101F homozygous viable T(3;4)Y291 80-81;101F homozygous viable T(3;4)Y320 88D;101F homozygous viable T(3;4)Y391 98F11-12;101F T(3;4)Y403 67E3-4;101F T(3;4)Y425 83A:101F homozygous viable T(3;4)Y434 80-81;101F T(3;4)Y446 70D;101F T(3;4)Y449 88E4-6;101F T(3;4)Y477 75C;101F T(3;4)Y494 98B;101F T(3;4)Y495 70C;101F homozygous viable T(3;4)Y512 + In(3R) 94B-C;96E;101F