# Df(2)M-33a: see Df(2R)M60E # Df(2L)061b cytology: Df(2L)38F7;39A6. origin: X ray induced. references: Siegel, 1981, Genetics 98: 505-27. # Df(2L)1: see Df(2L)TW1 # Df(2L)2: see Df(2L)TW2 # Df(2L)3: see Df(2L)TW3 # Df(2L)9: see Df(2L)TW9 # Df(2L)12: see Df(2L)TW12 # Df(2L)30A;C cytology: Df(2L)30A;30C (Laverty). references: Schupbach and Wieschaus, 1989, Genetics 121: 101- 17. genetics: Deficient for mat(2)cellQC13, mat(2)cellRH36, rem. # Df(2L)50: see Df(2L)TW50 # Df(2L)64j cytology: Df(2L)34D1-2;35B9 - C1. origin: X ray induced. discoverer: E.H. Grell, 1964. references: Grell, Jacobson, and Murphy, 1968, Annals N.Y. Acad. Sci. 151: 441-55. Nash, 1970, Genetics 64: 471-79. Woodruff and Ashburner, 1979, Genetics 92: 117-32. Gubb, Shelton, Roote, McGill, and Ashburner, 1984, Chromosoma 91: 54-64. Gubb, Roote, Harrington, McGill, Durrant, Shelton, and Ash- burner, 1985, Chromosoma 92: 116-23. Lasko and Ashburner, 1988, Nature (London) 335: 611-17. genetics: Deficient for l(2)34Db-ck but not M(2)30A, vasa or M(2)36F. Suppresses H. molecular biology: Left breakpoint 13.5 - 17.6 kb distal to the 0 point of the 35B-C walk of Lasko and Ashburner ("+" values to right, "-" values to left). # Df(2L)65: see Df(2L)TW65 # Df(2L)68: see Df(2L)TW68 # Df(2L)75c: see In(2L)75c # Df(2L)81: see Df(2L)L138D # Df(2L)84: see Df(2L)TW84 # Df(2L)119: see Df(2L)TW119 # Df(2L)130: see Df(2L)TW130 # Df(2L)137: see Df(2L)TW137 # Df(2L)150: see Df(2L)TW150 # Df(2L)158: see Df(2L)TW158 # Df(2L)161: see Df(2L)TW161 # Df(2L)201: see Df(2L)TW201 # Df(2L)202: see Df(2L)TW202 # Df(2L)203: see Df(2L)TW203 # Df(2L)282 cytology: Df(2L)25F2-3;25F4-26A1. # Df(2L)330: see Df(2L)TW330 # Df(2L)429.9: see T(2;3)429.9 # Df(2L)2802 cytology: Df(2L)25F2-3;25F4-26A1. origin: Induced by ethyl methanesulfonate. references: Kotarski, Pickert, and MacIntyre, Genetics 105: 371-86. genetics: Includes break of T(Y;2)G105. Deficient for l(2)25Fb and l(2)25Fd. # Df(2L)50075a: see Df(2L)Gpdh75 # Df(2L)50078a: see Df(2L)Gpdh78 # Df(2L)A: Deficiency (2L) Aaron origin: X ray induced; selected as ADH null on 1-penten-3-ol. discoverer: Aaron. deficiency cytology ref ( genetics _______________________________________________________________________ Df(2L)A47 34E1;35B2 1, 2, 4 wb--osp- Df(2L)A48 35B2-3;35D5-7 1, 2, 3, 4, 6 osp--lace- Df(2L)A63 / not visible 2, 3, 4 osp--Adh- Df(2L)A72 35B2-3;35B7-8 1, 2, 3, 5, 6 osp--l(2)35Cb- *Df(2L)A76 ` 1 Adh- *Df(2L)A167 ` 1 Adh- Df(2L)A178 / - 35B1-2;35B1-2 2, 3, 4, 5 noc--Adh- Df(2L)A215 35A3;35B7-8 1, 2 wb--rd- Df(2L)A217 34F5;35B3 1, 2 l(2)34Fd--Adh- Df(2L)A220 35B1-2;35B9 2 osp--l(2)35Cb- Df(2L)A245 35A4;35B2 2, 3 l(2)35Ba--Adh- Df(2L)A246 34F4;35D3-4 1, 2 wb--l(2)35Dg- Df(2L)A260 35B1-2;35B1-2 2, 3, 4 l(2)35Ba--Adh- Df(2L)A263 34E5-F1;35C3-9 2 l(2)34Fa--l(2)35Cd- Df(2L)A264 35B1-3;35B8-9 2, 5 osp--l(2)35Cb- Df(2L)A266 35B2-3;35B2-3 2 l(2)35Ba--Adh- Df(2L)A267 | 35B2-3;35B10-C1 2, 3 noc--vasa- Df(2L)A376 34E3;35C4-5 1, 2, 3 rk--dgl- Df(2L)A377 34F1-4;35D5-7 1, 2 wb--l(2)35Dd- Df(2L)A379 n - 35B1-3;35B1-3 + 2 noc--Adh- In(2LR)35B1-3; 40-41;57A8-10 *Df(2L)A385 ` 1 Df(2L)A400 i 35A1-4;35B10 1, 2, 3 pu--l(2)35Cb- Df(2L)A445 - not visible 2 noc--Adh- Df(2L)A446 see Tp(2;2)A446 ( 1 = Aaron, 1979, Mutat. Res. 63: 127-37; 2 = Ashburner, Aaron, and Tsubota, 1982, Genetics 102: 421-35; 3 = Ash- burner, Detwiler, Tsubota, and Woodruff, 1983, Genetics 104: 405-31; 4 = Gubb, Roote, Harrington, McGill, Durrant, Shelton, and Ashburner, 1985, Chromosoma 92: 116-23; 5 = Gubb, Roote, McGill, Shelton, and Ashburner, 1986, Genetics 112: 551-75; 6 = Gubb, Shelton, Roote, McGill, and Ashburner, 1984, Chromosoma 91: 54-64. | Right breakpoint mapped to the DNA at about 2.5 kb in the 35B-C walk of Lasko and Ashburner, 1988, Nature (London) 335: 611-17 ("+" values to right, "-" values to left). / Df(2L)A63 induced simultaneously with, but separable from, T(2;3)CA1 and T(2;3)CA2; Df(2L)A178 induced simultaneously with, but separable from, T(2;3)CA3. ` Lethal with Df(2L)A47 and Df(2L)A48. - Semilethal with noc. Males and females homozygous viable and fertile with strong noc and osp phenotypes. Lethal with Df(2L)b75 but viable and rk with Df(2L)b-L. Another reference: Simpson, 1983, Genetics 105: 615-32. n new order: 21 - 35B1-3|57A8-10 - 40-41|35B1-3 - 40-41|57A8-10 - 60. - Males and females homozygous viable and fertile. i Induced simultaneously with, but separable from, T(2;3;4)CA4. # Df(2L)A1: see Df(2L)pr-A1 # Df(2L)A16: see Df(2L)pr-A16 # Df(2L)a17 cytology: Df(2L)35C;36A. discoverer: Roth. references: Wustmann, Szidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. # Df(2L)A20: see Df(2L)pr-A20 # Df(2L)a25 cytology: Df(2L)35C;36A. discoverer: Roth. references: Wustmann, Sidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. # Df(2L)A244 cytology: Not visible cytologically but believed, on the basis of complementation data, to be a deficiency in 2L. origin: X ray induced. references: Siegel, 1981, Genetics 98: 505-27. # Df(2L)Adh1: see Df(2L)nNxF1 # Df(2L)Adh2: see Df(2L)nNxF2 # Df(2L)ade2 origin: Induced by hybrid dysgenesis. references: Tiong, Keizer, Nash, Bleskan, and Patterson, 1989, Biochem. Genet. 27: 333-48. genetics: Deficient for ade2. deficiency cytology ________________________________ Df(2L)ade2-1 Df(2L)25F;26B5-6 Df(2L)ade2-2 Df(2L)25F2-3;26DE Df(2L)ade2-3 Df(2L)26A;26B5-6 # Df(2L)Adh78 cytology: Df(2L)35B1;35D5-7. origin: Spontaneous in dysgenic strain T-007; selected as ADH null on 1-penten-3-ol. discoverer: Bencze. synonym: Df(2L)l78l3. references: Ashburner, Tsubota, and Woodruff, 1982, Genetics 102: 401-20. genetics: Deficient for l(2)35Ba-l(2)35Dg. # Df(2L)AdhnBR41 origin: Induced by ENU. discoverer: Lee. genetics: Deficient for l(2)34Fa-Adh. # Df(2L)al: Deficiency (2L) aristaless cytology: Df(2L)21B8-C1;21C8-D1. origin: X ray induced. discoverer: E. B. Lewis, 1940. references: 1945, Genetics 30: 147-51. Korochkina and Golubovsky, 1978, DIS 53: 197-200. Nusslein-Volhard, Wieschaus and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. genetics: Deficient for al, ex, ush and ds but not for lgl, net, or S. Homozygotes lethal, heterozygotes Minute. Hetero- zygotes with In(2LR)al8 survive poorly; escapers have reduced aristae, broad thoraces, arched wings, incomplete veins, and large eyes (Koroshkina and Golubovsky, 1978). # Df(2L)ARR1 cytology: Df(2L)35A3-4;35B9-C1. new order: 21 - 35A3-4|YL|y+ ac+|YS|35B9-C1 - 60. origin: X-ray-induced reconstitution of chromosome 2 from YP2D of T(Y;2)A80 and 2PYD of T(Y;2)R15. references: Woodruff and Ashburner, 1979, Genetics 92: 117-32. Gubb, Shelton, Roote, McGill, and Ashburner, 1984, Chromosoma 91: 54-64. genetics: Deficient for el-Su(H); includes Adh. Carries y+ac+ from T(Y;2)R15. # Df(2L)ast: Deficiency (2L) asteroid origin: / ray induced. references: Roberts, Brock, Rudden, and Evans-Roberts, 1985, Genetics 109: 145-56. genetics: Deficient for ast. deficiency cytology ___________________________________ Df(2L)ast1 21C7-8;23A1-2 Df(2L)ast2 21D1-2;22B2-3 Df(2L)ast3 21D1-2;21E1-2 Df(2L)ast4 21D1-2;21E1-2 Df(2L)ast5 21E1-2;21F3-22A1 Df(2L)ast6 21E1-2;21E2-3 Df(2L)ast10 ( 21D2-3;22A1-2 ( From complementation data. # In(2L)b: Inversion (2L) black inversion cytology origin ref ( genetics _________________________________________________________________ In(2L)b79d5 34D4;35B10 neutrons 1 lethal In(2L)b80c2 34C7;34D6-7 / ray 2 b In(2L)b81f3 34D2-4;35B10 neutrons 1 b; homozygous viable In(2L)b81l7 34D2-4;40F / ray 1 lethal In(2L)b82c44 34D4;40F neutrons 1 b; homozygous viable but sterile In(2L)b83b2 34D4;35B10 / ray 1 lethal In(2L)b85f2 33A1-2;35E3-4 + neutrons 1 lethal Df(2L)34D2-4; 34E6-F1 ( 1 = Alexandrov and Alexandrova, 1986, DIS 63: 159-61; 2 = Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. # Df(2L)B5: see Df(2L)pr-B5 # Df(2L)B10-1: see T(Y;2;3)B10-1 # Df(2L)B80: see T(Y;2)B80 # Df(2L)B119 cytology: {Df(2L)39D-E} (not cytologically detectable). origin: / ray induced. references: Siegel, 1981, Genetics 98: 505-27. # Df(2L)B209: see T(Y;2)B209 # Df(2L)C cytology: Deficient for most of the 2L heterochromatin. (40;40). origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes. synonym: Df(2L)PR31. references: Hilliker and Holm, 1975, Genetics 81: 705-21. genetics: Deficient for lt. # Df(2L)C' cytology: Deficient for much of the 2L heterochromatin and duplicated for much of the 2R heterochromatin. origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes. synonym: Df(2L)PR31. references: Hilliker and Holm, 1975, Genetics 81: 705-21. Hilliker, 1976, Genetics 83: 765-82. genetics: Deficient for 28 EMS-induced lethal alleles in seven complementation groups (Hilliker, 1976); duplicated for rl+ with an rl+ locus on each side of the centromere (Hilliker, 1981, DIS 56: 72-74). # Df(2L)C2: see Df(2L)L138D-C2 # Df(2L)C15: see Df(2L)L138D-C15 # Df(2L)C75RL: see In(2L)75cLC158.1R #*Df(2L)C263: Deficiency (2L) Crossover suppressor cytology: Df(2L)25F;26F. origin: Associated with In(2L)C263. # Df(2L)cl: Deficiency (2L) clot origin: X ray induced. genetics: Deficient for cl and surrounding lethal complementa- tion groups from l(2)25Eb to l(2)25Eg (Kotarski et al., 1983). deficiency cytology ref ( genetics _____________________________________________________________________ Df(2L)cl1 25D2-4;25F2-4 1, 3, 5, 6 tkv--E(var)- Df(2L)cl2 25D2-4;25F2-4 1, 3, 5, 6 tkv--E(var)- Df(2L)cl7 | 25D5-6;26A7 1, 2, 4, 6, 7 l(2)25De- Df(2L)cl-h1 / 25D4-5;25F1-2 5, 6 tkv--mid - Df(2L)cl-h2 / 25D6;25E4-5 5, 6 l(2)25De--l(2)26Aa- Df(2L)cl-h3 / 25D2-3;26B2-5 6 tkv- Df(2L)cl-h4 / 25D6;25F3-4 5, 6 l(2)25Ea--l(2)25Ef - ( 1 = Ashburner, Faithfull, Littlewood, Richards, Smith, Vel- issariou, and Woodruff, 1980, DIS 55: 193-95; 2 = Knipple and MacIntyre, 1984, Mol. Gen. Genet. 198: 75-83; 3 = Kotarski, Pickert, and MacIntyre, 1983, Genetics 105: 371-86; 4 = Racine, Langley, and Voelker, 1980, Environ. Mutagen. 2: 167-77; 5 = Semeshin and Szidonya, 1985, DIS 61: 148-54; 6 = Szidonya and Reuter, 1988, DIS 67: 77-79 and 1988, Genet. Res. 51: 197-208; 7 = Velis- sariou and Ashburner, 1980, Chromosoma 77: 13-27. | Enhances variegation of In(1)wm4 and In(1)y3P (Locke, Kotar- ski, and Tartof, 1988, Genetics 120: 181-98). / Isolated over Dp(2;2)B3 = Dp(2;2)23E2-3;26E2-F1. # Df(2L)CyLtR: see In(2L)CyLtR #*Df(2L)d: Deficiency (2L) dachs origin: Spontaneous in d stock. discoverer: Bridges, 15j6. synonym: dl: dachs-lethal. references: Bridges and Morgan, 1919, Carnegie Inst. Washington Publ. No. 278: 277. genetics: Homozygous lethal. Gives decreased crossing over in d-b region. # Df(2L)D cytology: Deficient for more than one-half of the proximal 2L heterochromatin. origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes. references: Hilliker and Holm, 1975, Genetics 81: 705-21. Hilliker, 1976, Genetics 83: 765-82. genetics: Deficient for four EMS-induced semilethal loci proxi- mal to lt. other information: Six such deficiencies recovered. # Df(2L)D' cytology: Deficient for more than one-quarter of the proximal 2L heterochromatin. origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes. references: Hilliker and Holm, 1975, Genetics 81: 705-21. Hilliker, 1976, Genetics 83: 765-82 genetics: Deficient for two EMS-induced lethal loci proximal to lt. Adults very small and late in hatching. other information: Eleven such deficiencies recovered. # Df(2L)D6: see T(Y;2)D6 # Df(2L)dl2034: see Df(2L)H20 # Df(2L)dl-H20: see Df(2L)H20 # Df(2L)do1 cytology: Df(2L)35B1-2;35D2. origin: Diepoxyoctane induced. discoverer: Detwiler. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. Ashburner, Tsubota, and Woodruff, 1982, Genetics 102: 401-20. genetics: Deficient for l(2)34Fd-sna. Includes el, noc, Adh, osp, and rd. # Df(2L)dp: Deficiency (2L) dumpy deficiency cytology origin ref ( genetics | ____________________________________________________________________ Df(2L)dp 25A3-4;25B spont / 1 dp- Df(2L)dp79b 22A2-3;22D5-E1 Df(2L)dp-h19 ` 24F1-2;24F6-7 X ray 2, 3 l(2)24Eb--dp- Df(2L)dp-h24 ` not visible X ray 3 M(2)25A--dp- Df(2L)dp-h25 ` 24E4;25B2 X ray 2, 3 dw24F--l(2)25Ac- Df(2L)dp-h28 ` 24D8;24F6-7 X ray 2, 3 l(2)24Ea--dp- ( 1 = Lutkin and Baker, 1979, Mutat. Res. 61: 221-27; 2 = Semeshin and Szidonya, 1985, DIS 61: 148-54. 3 = Szidonya and Reuter, 1988, DIS 67: 77-79 and 1988, Genet. Res. 51: 197-208; | Includes complementation groups localized in the deleted regions by Szidonya (unpubl.). / In mei-W68 male. ` Isolated over Dp(2;2)B3 = Dp(2;2)23E2-3;26E2-F1. # Df(2L)dp-cl: Deficiency (2L) dumpy-clot origin: X ray induced. references: Szidonya and Reuter, 1988a, DIS 67: 77-79. 1988b, Genet. Res. 51: 197-208. genetics: Deficient for dp-cl; includes haplo-insufficient genes. deficiency ( cytology _________________________________ Df(2L)dp-cl-h1 24F7-25A1;26A2-3 Df(2L)dp-cl-h2 24E4-F1;26B9-C1 Df(2L)dp-cl-h3 24F7-25A1;25E2-4 ( Isolated over Dp(2;2)B3 = Dp(2;2)23E2-3;26E2-F1. # In(2L)dpp: Inversion (2L) decapentaplegic genetics: Mutant for dpp. inversion cytology origin discov. ( ref | class _________________________________________________________________________ In(2L)dpp1 22E2-3;22F2-3 spont 9 1, 4 III In(2L)dpp2 22F1-2;28B X ray 5 1, 4 IV In(2L)dpp6 22F1-3;24F2-6 X ray 8 1, 3, 4 III In(2L)dpp8 22A1-2;22F1-2 X ray 8 1, 3, 4 III In(2L)dpp10 22E4-F1;23E2-4 X ray 8 1, 3, 4 III In(2L)dpp12 22E2-3;22F2-3 X ray 8 1, 3, 4 V In(2L)dpp17 22F1-3;27E X ray 8 1, 4 V In(2L)dpp36 ` 22F1-2;35E X ray 2 1, 3, 4 III? In(2L)dpp42 22F1-3;22F3-4 / ray 3 1 V In(2L)dpp50 22F2-3;27C / ray 3 1 I/II In(2L)dpp60 21E;22F / ray 6 1 III In(2L)dpp63 22F;39C-D / ray 6 1 V In(2L)dpp65 / 22F;34C;40 / ray 6 1 1 In(2L)dpp66 / 21E;22F1-2 + / ray 7 1 II Dp(3;2)21E-22F; 78F;80F In(2L)dpp67 21F;22F / ray 7 1 I In(2L)dpp86 / 22F;26C;35D-E / ray 1 1 EL *In(2L)dppho40 - 21D4-E1;22E2-3 X ray 4 1, 2, 4 I ( 1 = Blackman; 2 = Gelbart; 3 = Irish; 4 = E.B. Lewis; 5 = Loos; 6 = L. Posakony; 7 = Segal; 8 = Spencer; 9 = Tung. | 1 = Gelbart; 2 = Lewis, 1945, Genetics 30: 137-66; 3 = Segal and Gelbart, 1985, Genetics 109: 119-43; 4 = Spencer, Hoffmann, and Gelbart, 1982, Cell 28: 451-61. / New order: In(2L)dpp65 = 21A - 22F|34C - 22F|40 - 34C|40 - 60F. In(2L)dpp66 = 21A - 21E|78F - 80F|22F - 21E|22F - 60F. In(2L)dpp86 = 21A - 22F|26C - 22F|35D-E - 26C|35E - 60F (breakpoints tentative). ` Synonym: In(2L)dppd36 . (Irish and Gelbart, 1987, Genes Dev. 1: 868-79. - Synonym: *In(2L)ho40 . Mutant for ho but not S or ast. Homozygous viable. # Df(2L)dpp21: see T(2;3)dpp21 # Df(2L)DS origin: Induced by triethylenemelamine. references: Sinclair, Moore, and Grigliatti, 1980, Genetics 94: s96. Moore, Sinclair, and Grigliatti, 1981, Genetics 105: 327-44. deficiency cytology genetics _______________________________________ Df(2L)DS5 39A1-2;39E7-F1 pr--His- Df(2L)DS6 38F5;39E7-F1 crc--His- Df(2L)DS8 39A6-7;39D2-3 crc- Df(2L)DS9 39A1-2;39B2-3 crc+ His+ # Df(2L)DTD2: see Tp(2;1)DTD2 # Df(2L)DTD33: see Tp(2;3)DTD33 # Df(2L)DTD48 cytology: Df(2L)22E2-4;22F4-23A1. origin: X ray induced. references: Spencer, Hoffmann, and Gelbart, 1982, Cell 28: 451-61. genetics: Deficient for the entire dpp locus. # Df(2L)E: see T(2;3)E # Df(2L)E53 cytology: Not visibly deficient. origin: Induced by ethyl methanesulfonate. references: T.R.F. Wright, 1983. genetics: Deficient for l(2)36Fc and msl-1, but not for l(2)36Fb, l(2)36Fd, or l(2)36Fe. Lethal over Df(2L)TW3, Df(2L)E71, Df(2L)M36F-S6, and Df(2L)M36F-S5; viable over Df(2L)TW119. # Df(2L)E55 cytology: Df(2L)37D2-E1;37F5-38A1. origin: Induced by ethyl methanesulfonate. references: Wright, Hodgetts, and Sherald, 1976, Genetics 84: 267-85. Brittnacher and Ganetzky, 1983, Genetics 103: 659-73. Nusslein-Volhard, Wieschaus and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. genetics: Deficient for ref(2)P and spi. Lethal over Df(2L)TW330, Df(2L)VA15, Df(2L)VA20, Df(2L)VA22, Df(2L)VA23, Df(2L)VA25, Df(2L)TW9, Df(2L)TW12, l(2)37Da, l(2)37Db, l(2)37Fa, l(2)37Fb, l(2)37Fc, and l(2)37Fd. Viable, but shows non-transparent wing phenotype over Df(2L)TW150, Df(2L)TW84, and Df(2L)OD16. # Df(2L)E66: Deficiency (2L) Enhancer of variegation cytology: Df(2L)25F2-3;26A1-B1. origin: P-element induced mutagenesis. references: Locke, Kotarski, and Tartof, 1988, Genetics 120: 181-98. genetics: Enhances position-effect variegation of In(1)wm4. Recessive lethal. # Df(2L)E71 cytology: Df(2L)36F2-6;37C6-D1. origin: Induced by ethyl methanesulfonate. references: Wright, Hodgetts. and Sherald, 1976, Genetics 84: 267-85. Belote and Lucchesi, 1980, Genetics 96: 165-86. Wright, Beermann, Marsh, Bishop, Steward, Black, Tomsett, and Wright, 1981, Chromosoma 83: 45-58. genetics: Deficient for msl-1 - fs(2)TW1 (Wright, 1983) but not for dl or l(2)37Da. Lethal over Df(2L)M36F, Df(2L)E53, l(2)36Fc, l(2)36Fd, l(2)36Fe, and Df(2L)SDrv77. # Df(2L)E110 cytology: Df(2L)25F3-26A1;26D3-11. origin: P-element induced mutagenesis. references: Locke, Kotarski, and Tartof, 1988, Genetics 120: 181-98. genetics: Enhances position-effect variegation of In(1)wm4. Recessive lethal. # Df(2L)E(SD): Deficiency (2L) Enhancer of Segregation Distorter origin: / ray induced in SD-5 chromosome. references: Ganetzky, 1977, Genetics 86: 321-55. genetics: Deficient for l(2)40Fa - l(2)40Ff. Partial revertant of Sd. deficiency cytology synonym male fecundity ____________________________________________________________ Df(2L)E(SD)1 ( 40A-B;40E Df(2L)SDRev-1 intermediate Df(2L)E(SD)3 | 40A-B;40F Df(2L)SDRev-3 low Df(2L)E(SD)36 40A-B;40F Df(2L)SDRev-36 low ( Involved in translocation of 3R tip to base of 2R [T(2;3)E(SD)1]. | Carries In(2L)E(SD) = In(2L)29E;30A. # Df(2L)ed1: Deficiency (2L) echinoid cytology: Df(2L)24A3-4;24D3-4. discoverer: Szidonya. synonym: Df(2L)ed-Sz1. references: Reuter and Szidonya, 1983, Chromosoma 88: 277-85. Szidonya and Reuter, 1988a, DIS 67: 77-79. 1988b, Genet. Res. 51: 197-208. genetics: Includes ed but not M(2)24D or M(2)24F. # Df(2L)ed2 cytology: Df(2L)24A3-4;24D3-4. discoverer: Szidonya. synonym: Df(2L)ed-Sz2. references: Reuter and Szidonya, 1983, Chromosoma 88: 277-85. genetics: Includes ed but not M(2)24D or M(2)24F. # Df(2L)ed-dp: Deficiency (2L) echinoid to dumpy cytology: Df(2L)24C3-5;25A2-3. origin: X ray induced. references: Szidonya and Reuter, 1988a, DIS 67: 77-79. 1988b, Genet. Res. 51: 197-208. genetics: Deficient for ed-dp; includes haplo-insufficient genes. Isolated over Dp(2;2)B3 = Dp(2;2)23E2-3;26E2-F1. # Df(2L)el: Deficiency (2L) elbow deficiency cytology origin ref ( genetics ______________________________________________________________________ Df(2L)el15 35B1-2;35C5 / ray 5 l(2)34Fc--l(2)35Cb- Df(2L)el16 not visible / ray 5 el--noc- Df(2L)el17 34F1-2;35A4 / ray 5 wb--Adh- Df(2L)el18 see In(2L)el18 Df(2L)el20 34F4;35C5 EMS 5 wb--l(2)35Da- Df(2L)el28 / ray el--Su(H)- Df(2L)el77 35A1-3;35B3 / ray 3, 6 wb--Adh- Df(2L)el80f1 34E3;35D7 / ray 1, 2, 4 rk--lace- Df(2L)el80i1 34E1-2;35C2-3 / ray 1 l(2)34Eb--l(2)35Cb- Df(2L)el81i1 34F5;35B1-2 / ray 1 wb--Adh- Df(2L)el82f1 34E1-2;35C3-5 EMS 1 l(2)34Eb--l(2)35Ce- ( 1 = Angel; 2 = Ashburner, Detwiler, Tsubota, and Woodruff, 1983, Genetics 104: 405-31; 3 = Ashburner, Faithfull, Lit- tlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95; 4 = Ashburner and Harrington, 1984, Chromo- soma 89: 329-37; 5 = G. Johnson; 6 = Woodruff and Ash- burner, 1979, Genetics 92: 117-32. # Df(2L)esc10 cytology: Df(2L)33A8-B1;33B2-3 (G. Richards). origin: / ray induced. references: Struhl, 1981, Nature 293: 36-41. Frei, Baumgartner, Edstrom, and Noll, 1985, EMBO J. 4: 979- 87. Frei, Schuh, Baumgartner, Burri, Noll, Jurgens, Seifert, Nauber, and Jackle, 1988, EMBO J. 7: 197-204. genetics: Deficient for esc but not for sal. Homozygotes viable and extreme esc when mother esc+/esc-, but lethal in first larval instar with homoeotic transformation of segments when mother esc-/esc-. Heterozygotes with esc2, esc4, esc5, esc6, esc8, or esc9 show same extreme phenotypes as homozy- gotes. molecular biology: Embryos deficient for esc show indiscrim- inate expression of segment-specific homeotic genes (Struhl and Akam, 1985, EMBO J. 4: 3259-64). Distal breakpoint mapped to the DNA at about -310 to -290 kb and proximal break- point mapped at about +70 kb ("-" values to right, "+" values to left) in the F walk of Frei et al., 1985. # Df(2L)esc-P2-0 cytology: Df(2L)33A1-2;33B1-2. origin: Hybrid dysgenesis. discoverer: Struhl. references: Jurgens, 1988, EMBO J. 7: 189-96. Frei, Schuh, Baumgartner, Burri, Noll, Jurgens, Seifert, Nauber, and Jackle, 1988, EMBO J. 7: 197-204. genetics: Deficient for sal and esc. molecular biology: Distal breakpoint mapped to the DNA at about -476 to -442 kb (Frei et al., 1985). # Df(2L)esc-P3-0 cytology: Df(2L)33A1-2;33E. origin: Hybrid dysgenesis. discoverer: Struhl. references: Jurgens, 1988, EMBO J. 7: 189-96. Frei, Schuh, Baumgartner, Burri, Noll, Jurgens, Seifert, Nauber, and Jackle, 1988, EMBO J. 7: 197-204. genetics: Deficient for sal and esc. # Df(2L)F cytology: Deficient for heterochromatin between lt and the secondary constriction. origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes. references: Hilliker and Holm, 1975, Genetics 81: 705-21. Hilliker, 1976, Genetics 83: 765-82. genetics: M and lt+ phenotypes. Deficient for lethal loci l(2)40Fa and l(2)40Fd (Hilliker, 1976). other information: Two such deficiencies recovered. # Df(2L)FB15: see Df(2L)L138D # Df(2L)fn: Deficiency (2L) formaldehyde induced origin: Formaldehyde induced. Selected as ADH null on 1- penten-3-ol. discoverer: Sofer. deficiency cytology ref ( genetics ________________________________________________________________________ Df(2L)fn1 34F4-35A1;35D5-7 3, 4, 7, 8 wb--lace- Df(2L)fn2 35A3;35B2 3, 4, 7, 8 el--Adh- Df(2L)fn3 | 35B1;35B3-4 3, 4, 5, 6, 7, 8 l(2)35Ba--l(2)35Bb- Df(2L)fn5 34F5;35C3 7 wb--l(2)35Cb- Df(2L)fn7 34E1-2;35B3-5 2, 3, 5, 6, 7, 8 j--Adh- Df(2L)fn12 34D3;35B10 7 {rk--ck-} Df(2L)fn15 35B1-2;35B7-C5 7 el--ck- Df(2L)fn26 34E3;35D8-E1 3, 7 j--l(2)35Ea- Df(2L)fn27 | 35B1;35D1-2 2, 3, 4, 5, 7 noc--lace- Df(2L)fn30 / 34C6-7;35B9-C1 7 l(2)34Db--vasa- Df(2L)fn31 34D3;35B3-5 2, 6, 7 l(2)34Db--l(2)35Bf- Df(2L)fn36 35A3;35B4 7 wb--Adh- Df(2L)fn52 | not visible 1 osp- Adh- ( 1 = Ashburner; 2 = Ashburner, 1982, Genetics 101: 447-59; 3 = Ashburner, Detwiler, Tsubota, and Woodruff, 1983, Genet- ics 104: 405-31; 4 = Ashburner, Tsubota, and Woodruff, 1982, Genetics 102: 401-20; 5 = Gubb, Roote, Harrington, McGill, Durrant, Shelton, and Ashburner, 1985, Chromosoma 92: 116-23; 6 = Gubb, Shelton, Roote, McGill, and Ash- burner, 1984, Chromosoma 91: 54-64; 7 = O'Donnell, Mandell, Krauss, and Sofer, 1977, Genetics 86: 553-66; 8 = Woodruff and Ashburner, 1979, Genetics 92: 117-33. | See deficiency map under l(2)35 for molecular coordinates of left breakpoints. / Right breakpoint around 12.5 kb in 35C walk of Lasko and Ashburner (1988, Nature 335: 611-17). # Df(2L)G cytology: Df(2L)36B5-6;40F. origin: Aneuploid segregant from T(2;Y)G/+. # Df(2L)GdhA: see Df(2L)GpdhA # Df(2L)GM: see Df(2L)Sco-1 # Df(2L)Got2: Deficiency (2L) Glutamate oxaloacetic transaminase cytology: Df(2L)22A;22B5-8. origin: Segmental aneuploid from T(Y;2)J69 and T(Y;2)H56. references: Racine, Langley and Voelker, 1980, Environ. Mutagen. 2: 167-77. Chase and Kankel, 1987, J. Neurobiol. 18: 15-41. genetics: Deficient for Got2. # Df(2L)Gpdh75: Deficiency (2L) Glycerol phosphate dehydrogenase cytology: Df(2L)25F2-3;25F4-26A1. origin: / ray induced. discoverer: Voelker. synonym: Df(2L)50075a. references: Racine, Langley, and Voelker, 1980, Environ. Mutagen. 2: 167-77. Kotarski, Pickert, and MacIntyre, 1983, Genetics 105: 371-86. genetics: Deficient for Gpdh. # Df(2L)Gpdh78 cytology: Not visibly deficient. origin: X ray induced. discoverer: Voelker. synonym: Df(2L)50078a. references: Racine, Langley, and Voelker, 1980, Environ. Mutagen. 2: 167-77. Kotarski, Pickert, and MacIntyre, 1983, Genetics 105: 371-86. genetics: Deficient for l(2)25Fc - Gpdh. Lethal with Df(2L)GpdhA and Df(2L)cl7. # Df(2L)Gpdh101 cytology: Df(2L)25E1-2;26A2-5. references: Cook, Shaffer, Bewley, MacIntyre, and Wright. genetics: Deficient for Gpdh. # Df(2L)GpdhA cytology: Df(2L)25D7-E1;26A8-9 (Kotarski et al., 1983). origin: X ray induced. synonym: Df(2L)GdhA. references: Grell, 1967, Science 158: 1319-20. 1968, Genetics 60: 184-85. O'Brien and MacIntyre, 1972, Genetics 71: 127-38. Racine, Langley, and Voelker, 1980, Environ. Mutagen. 2: 167-77. Kotarski, Pickert, and MacIntyre, 1983, Genetics 105: 371-86. Knipple and MacIntyre, 1984, Mol. Gen. Genet. 198: 75-83. genetics: Deficient for cl-l(2)26Ae (Kotarski et al., 1983). Enhances variegation of In(1)wm4 and In(1)y3P (Locke, Kotar- ski, and Tartof, 1988, Genetics 120: 181-98. # Df(2L)GT4 cytology: Df(2L)34F3;35B2. origin: / rays. discoverer: Durrant. genetics: Deficient for l(2)34Fa--noc-. # Df(2L)GT5 origin: / rays. discoverer: Durrant. genetics: Deficient for b-noc. #*Df(2L)H: see Tp(2;Y)H # Df(2L)H20 cytology: Df(2L)36A8-9;36E3-4. origin: X ray induced. discoverer: Nusslein-Volhard. synonym: Df(2L)dl2034; Df(2L)dl-H20. references: Simpson, 1983, Genetics 105: 615-32. Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. Steward and Nusslein-Volhard, 1986, Genetics 113: 665-78. genetics: Deficient for l(2)36Aa through ninaD, but not for M(2)36F. Lethal over Df(2L)TW119, Df(2L)M36F-S5, Df(2L)TW137, Df(2L)T317, Df(2L)TW201, Df(2L)203, Df(2L)330, and Df(2L)VA18. # Df(2L)H68 cytology: Df(2L)36B-C1;37A1-B1 (Wieschaus). origin: X ray induced. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. genetics: Deficient for dl, l(2)36Ba - l(2)37Ac but not Mhc. Lethal over Df(2L)H20, Df(2L)T317, Df(2L)TW119, Df(2L)TW137, Df(2L)M36F-S5, Df(2L)VA18, Df(2L)TW201, and Df(2L)50. # Df(2L)H151 cytology: Df(2L)25F;26A. references: Kotarski, Pickert, and MacIntyre, 1983, Genetics 105: 371-86. # Df(2L)hk18: Deficiency (2L) hook cytology: Df(2L)36E4-6;37B9-C1. origin: X ray induced in SD-72 chromosome. references: Brittnacher and Ganetzky, 1983, Genetics 103: 659-73. genetics: Deficient for l,(2)36Fb, Tft, and hk, but not M(2)36F. Lethal over Df(2L)M36F-S5, Df(2L)M36F-S6, Df(2L)TW158, Df(2L)TW130, and l(2)36Fb-Dox. molecular biology: Proximal breakpoint between -52.15 and -50.55 kb (see deficiency map under l(2)37 for coordinates). # Df(2L)hk39 cytology: Df(2L)36F6-37A1;37D1-2. origin: X ray induced in SD-Roma chromosome. references: Brittnacher and Ganetzky, 1983, Genetics 103: 659-73. genetics: Deficient for Tft and hk but not l(2)37Db. Lethal over Df(2L)Sd57 and Df(2L)Sd77. # Df(2L)hk-UC1 origin: X ray induced in Canton-S. discoverer: Gibbs and Marsh. genetics: Deficient for l(2)31Ba - Dox-A2 but not for l(2)37Bg. molecular biology: Right breakpoint at -56.75 to -54.95 to the left of Ddc (-0.06 to +3.76). # Df(2L)hk-UC2 origin: From 15 generations of repeated backcrossing of Canton-S males to M strain females homozygous for nub b rdo hk pr cn. discoverer: Gibbs and Marsh. references: Eveleth and Marsh, 1986, Nucleic Acid Res. 4: 6169-83. genetics: Deficient for hk-l(2)37Cb - l(2)37Cc but not for l(2)37Cd. molecular biology: Right breakpoint at +8.15 to +10.95 to the right of Ddc (-0.06 to +3.76). # Df(2L)J: Deficiency (2L) Jammed origin: X ray induced as J revertants. synonym: Df(2L)J-der; Df(2L)J-rv. deficiency cytology ref ( genetics _____________________________________________________ Df(2L)J2 | 31B;32A 1, 2, 5 J--da- Df(2L)J4 | 31A-B;31F-32A 1, 2, 4 M(2)30A--da- Df(2L)J27 | 31B-E;32A 4, 5 J--da- Df(2L)J39 31A-B;32D-E 2, 4, 5 M(2)30A--abo- Df(2L)J77 3 J--l(2)54- Df(2L)J106 3 J--l(2)54- Df(2L)J233 3 J--l(2)54- ( 1 = Mange and Sandler, 1973, Genetics 73: 73-86; 2 = Sandler, 1975, Israel J. Med. Sci. 11: 1124-34; 3 = Salas and Lengyel, 1984, DIS 60: 243-44; 4 = Sandler, 1977, Genetics 86: 567-82; 5 = Voelker, Ohnishi, and Lang- ley, 1978, Biochem. Genet. 17: 769-83. | Lethal over da. # Df(2L)JK12 cytology: Df(2L)37D2-E1;38A8-C1 (Kennison). origin: / ray induced. discoverer: Kennison. genetics: pr-l(2)37Dc-Bl+; lethal in combination with T(Y;2)H174 = T(Y;2)YS;37D and Df(2L)TW158 = Df(2L)37B2- 8;37E2-F4. # Df(2L)L cytology: Df(2L)38B;40. origin: Segmental deficiency comprising the YP2D element of T(Y;2)P7 = T(Y;2)h9-10;38b and the 2PYD element of T(Y;2)B190 = T(Y;2)40. synonym: T(Y;2)P57LB190R. references: Khesin and Leibovitch, 1978, Mol. Gen. Genet. 162: 323-28. Chernyshev, Leibovitch, and Khesin, 1980, Mol. Gen. Genet. 178: 663-68. genetics: Deficient for His. Variegated w position effect in Dp(1;3)wvco weakened in Df(2L)L/+ flies. # Df(2L)L138D cytology: Df(2L)39A;39D-E, with indeterminate quantities of Y heterochromatin intercalated between the chromosome-2 break- points. origin: /-ray-induced reconstitutions of chromosome 2 from the YP2D element of T(Y;2)L138 and the 2PYD element of T(Y;2)B209, T(Y;2)B251, or T(Y;2)H54. Deficient for most but not all of the tandemly repeated Histone genes. discoverer: J. Siegel. references: 1981, Genetics 98: 505-29. genetics: Deficient for His. deficiency 2PYD component ____________________________________________ Df(2L)L138D-81 ( T(Y;2)H54 Df(2L)L138D-C2 T(Y;2)B209 Df(2L)L138D-C15 T(Y;2)B209 Df(2L)L138D-FB15 | T(Y;2)B251 Df(2L)L138D-X1 T(Y;2)B209 Df(2L)L138D-X14 T(Y;2)B209 Df(2L)L138D-XR T(Y;2)B209 ( Large segment of Hoechst-33258-bright, Y-derived material intercalated between second-chromosome breakpoints; neither bb+ nor any Y fertility factor included. | Produces M phenotype in heterozygotes. Presumably deficient for M(2)39F and therefore extends further to right than other Df(2L)L138D's. #*In(2L)ltm: Inversion (2L) light-mottled origin: X ray induced. discoverer: Hessler, 1957. references: 1958, Genetics 43: 395-403. genetics: Variegated for lt. inversion cytology ____________________________ *In(2L)ltm2 22F-23A;40B-F *In(2L)ltm20 32C;40B-F *In(2L)ltm26 27C;40B-F # Df(2L)M9: see In(2LR)M9 # Df(2L)M11: see Df(2L)M24F11 # Df(2L)M15: see Tp(2;Y)G-M15 # Df(2L)M18: see Df(2L)M36F18 # Df(2L)M24F: Deficiency (2L) Minute genetics: M phenotype. genetics deficiency cytology origin syn ref ( (cont) _______________________________________________________________________ Df(2L)M24F11 | 24D3-4; X ray M11 6, 8, 9 ang+ed--dp- 25A2-3 l(2)25Ad+ Df(2L)M24F-B |/ 24D8-E1; spont M-zB 1, 2, 3, ang+l(2)24EFa- 24F7-25A1 5, 6, 7, -dp-tkv+ 9 Df(2L)M24F-C 24D2-5; spont M-zC 4, 5 ed--dp- 25A2-3 l(2)cg+ ( 1 = Curry, 1939, DIS 12: 46; 2 = Duttagupta and Roy, 1984, DIS 60: 92; 3 = Duttagupta, Kar, and Roy, 1984, DIS 60: 93; 4 = Morgan, Bridges, and Schultz, 1938, Year-book- Carnegie Inst. Washington 37: 307; 5 = Morgan, Schultz, Bridges, and Curry, 1939, Year-book-Carnegie Inst. Washing- ton 38: 276-77; 6 = Reuter and Szidonya, 1983, Chromosoma 88: 277-85; 7 = Roy, Manna, and Duttagupta, 1984, J. Biosci. 6: 87-95; 8 = Semeshin and Szidonya, 1985, DIS 61: 148-61; 9 = Szidonya and Reuter, 1988, DIS 67: 77. | Suppresses position-effect variegation in In(1)wm4h. / Enhances bwV1 (Duttagupta et al., 1984). # Df(2L)M36F genetics: M phenotype. discov genetics deficiency cytology origin ( syn ref | (cont) ______________________________________________________________________ Df(2L)M36F18 36B3-8; M18 1 l(2)36Ba-- 36D1-E1 l(2)36Da- Df(2L)M36F-S5 / 36D1-E1; 1 M(2)HS5 2, 3 l(2)36Da- 36F1-37A1 -rdo-dl+ Df(2L)M36F-S6 ` 36E6-F1; 2 M(2)mS6 2, 3 l(2)36Fb- 36F7-9 -l(2)36Fe- ( 1 = In stock labelled M(2)HS5; 2 = X ray induced. | 1 = Mohler and Wieschaus; 2 = Schultz, 1933; 3 = Wright, Hodgetts, and Sherald, 1976, Genetics 84: 267-85. / Lethal over Df(2L)M36F-S6 (claimed by Schultz to complement this deficiency, but found by Wright not to do so). Also lethal over Df(2L)TW119, Df(2L)H20; Df(2L)TW50, Df(2L)TW137, Df(2L)E71, Df(2L)TW3, Df(2L)VA16, and Df(2L)hk18 (Wright). ` Lethal over Df(2L)M36F-S5, Df(2L)TW50, Df(2L)hk18, Df(2L)E71, Df(2L)TW3, and Df(2L)E53 (Wright). # Df(2L)M-B: see Df(2L)M24F-B # Df(2L)M-C: see Df(2L)M24F-C # Df(2L)M-HS5: see Df(2L)M36F-S5 # Df(2L)M-mS6: see Df(2L)M36F-S6 # Df(2L)M-zB: see Df(2L)M24F-B # Df(2L)M-zC: see Df(2L)M24F-C # Df(2L)Mdh: Deficiency (2L) Malate dehydrogenase cytology: Df(2L)30D-F;31F. origin: X ray induced. synonym: Df(2L)Mdh-2J. references: E. H. Grell, 1969, Genetics 61: s23. Sandler, 1977, Genetics 86: 567-82. genetics: J revertant. Deficient for M(2)30A-da. # Df(2L)N22-3 cytology: Df(2L)30A1-2;30D1-2. discoverer: Schupbach. references: Wustmann, Szidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. # Df(2L)N22-5 cytology: Df(2L)29D1-2;30C4-D1. discoverer: Schupbach. references: Wustmann, Szidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. # Df(2L)n7813 cytology: Df(2L)35B1;35D5-7. origin: Hybrid dysgenesis. discoverer: Bencze. genetics: Deficient for l(2)35Ba - l(2)35Dg-. # Df(2L)net18: see In(2LR)net18 # Df(2L)net deficiency cytology ref ( genetics ____________________________________________________ Df(2L)net62 | 21A;21B4-5 1, 3 net- l(2)gl- Df(2L)net-PM47C 21A1;21B6-7 2 net- Df(2L)net-PMC 21A1;21B6-7 2 net- kis- Df(2L)net-PMF 21A1;21B7-8 2 net- kis- ( 1 = Golubovsky, Kulakov, and Korochkina, 1978, Genetika 14: 294-305; 2 = Kennison; 3 = Korochkina and Golubovsky, 1978, DIS 53: 197-200. | X ray induced. # Df(2L)nNxF1 cytology: Df(2L)35B3;35B10 (Ashburner). origin: X ray induced. discoverer: Maroni. synonym: Df(2L)Adh1. genetics: Deficient for osp-l(2)35Cb. molecular biology: Left breakpoint mapped to the DNA (Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689- 706). # Df(2L)nNxF2 cytology: Df(2L)35B3;35B10 (Ashburner). origin: X ray induced. discoverer: Maroni. synonym: Df(2L)Adh2. genetics: Deficient for osp-l(2)35Cb. molecular biology: Left breakpoint mapped to the DNA (Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689- 706). # Df(2L)noc: Deficiency (2L) no-ocelli origin: / ray induced. references: Ashburner. deficiency cytology discoverer genetics ________________________________________________________________ Df(2L)noc10 34F1-2;35B1-2 Harrington l(2)34Fa--Adh- Df(2L)noc11 34E3;35A2 Harrington l(2)34Fa--l(2)35Cd- Df(2L)noc13 35A1-2;35B2 Harrington wb--Adh- Df(2L)noc20 ( 34F1-2;35B2 Roote l(2)34Fa--Adh- ( Induced in CyO, AdhnB. Adh deficient by molecular criteria (Karp). Df(2L)noc20/osp- flies have extreme Curly wings. Proximal DNA breakpoint between +11.8 and +13.7 kb (Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689-706). # Df(2L)NST origin: X ray induced in Canton-S males. discoverer: Gibbs and Marsh. references: Pentz and Wright, 1986, Genetics 112: 843-59. Marsh, Erfle, and Leeds, 1986, Genetics 114: 453-67. genetics: Deficient for l(2)37Bd - l(2)37Cg but not for l(2)37Da. molecular biology: Left breakpoint at -37.8 to -33.8 kb, approximately 30 kb distal to Ddc. # Df(2L)OD origin: Induced by diepoxybutane. deficiency discoverer ( genetics ___________________________________________________________ Df(2L)OD9 2 rdo+ hk--Ddc- ref(2)P+ Df(2L)OD12 2 ref(2)P+ l(2)37Fa- Df(2L)OD15 | 2, 3 hk--l(2)37Be- amd+ Df(2L)OD16 / 2 ref(2)P+ l(2)37Fd--l(2)37Fg- Df(2L)OD21 2 ref(2)P+ l(2)37Fc- Df(2L)OD-P5 1 ref(2)P- l(2)37Ea- l(2)37Fa- l(2)37Fb- ( 1 = Contamine, Peritjean, and Ashburner, 1989, Genetics 123: 525-33; 2 = Gay and Contamine; 3 = Wright. | Proximal DNA breakpoint between -64.65 and -65.25 kb (see deficiency map under l(2)37 for coordinates). / Only part of 38A deleted. Shows non-transparent wings when heterozygous with Df(2L)E55. # Df(2L)odd: Deficiency (2L) odd skipped cytology: Df(2L)21A;24B. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. genetics: Deficient for odd. # Df(2L)osp: Deficiency (2L) outspread origin: / ray induced. discoverer: Detwiler. references: Ashburner, Tsubota, and Woodruff, 1982, Genetics 102: 401-20. Ashburner, Detwiler, Tsubota, and Woodruff, 1983, Genetics 104: 405-31. deficiency cytology genetics _____________________________________________________ Df(2L)osp18 (| 35B1-2;35C4-5 osp--dgl- Df(2L)osp29 |/ 35B1-3;35E6 osp- l(2)35Bb-- l(2)35Eb- Df(2L)osp38 35A1-2;35C4-5 wb--l(2)35Cd- Df(2L)osp141 ` 34F5;35B5 l(2)34Fa--Adh- Df(2L)osp144 |- not evident noc--osp- Df(2L)osp204 | see Tp(3;2)osp204 noc--osp- ( Also see Simpson, 1983, Genetics 105: 615-32. | Left and/or right breakpoints mapped to the DNA (Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689-706). / Heterozygotes with Sco viable and without enhanced Sco phenotype. ` Induced simultaneously with T(2;3)CA7 and T(2;3)CA8. - Deleted for about 50 kb of DNA within both the osp and noc loci (S. McGill). Gubb, Roote, Harrington, McGill, Durrant, Shelton, and Ash- burner, 1985, Chromosoma 92: 116-23. # Df(2L)~~1a1 cytology: Df(2L)34D3;35B4 (Ashburner). origin: Hybrid dysgenesis; selected as ADH null. discoverer: Craymer. genetics: Deficient for l(2)34Db-l(2)35Bf; includes Adh. # Df(2L)PA4 cytology: Df(2L)35B1-3 + Df(2L)35D1;36A1-2. origin: / ray induced in Sco chromosome; selected as ADH null. discoverer: Angel. references: Ashburner, Detwiler, Tsubota, and Woodruff, 1983, Genetics 104: 405-31. Simpson, 1983, Genetics 105: 615-32. Ashburner and Harrington, 1984, Chromosoma 89: 329-37. genetics: Deficient for noc-Adh and sna-l(2)35Ec. Revertant for Sco. # Df(2L)PM references: Caggese, Caizzi, Bozzetti, Barsanti, and Ritossa, 1988, Biochem. Genet. 26: 571-84. deficiency cytology genetics _____________________________________ Df(2L)PM1 21A1;21B3-5 net- Gsi+ Df(2L)PM4 21A1;21B1-2 net- Gsi+ Df(2L)PM6 21A1;21B2-3 net- Gsi+ Df(2L)PM44 21A1;21B2-4 net- Gsi+ Df(2L)PM45 21A1;21B4-6 net- Gsi- Df(2L)PM47C 21A1;21B6-7 net- Gsi- Df(2L)PM51 21A1;21B3-5 net- Gsi+ Df(2L)PM59 21A1;21B3-5 net- Gsi+ Df(2L)PM82 21A1;21B2-4 net- Gsi+ Df(2L)PM91 21A1;21B4-6 net- Gsi- Df(2L)PMC 21A1;21B4-6 net- Gsi- Df(2L)PMF 21A1;21B7-8 net- Gsi- Df(2L)PMG 21A1;21B4-6 net- Gsi- # Df(2L)pr: Deficiency (2L) purple origin: X ray induced. synonym: pr may be omitted as in Df(2L)A1, Df(2L)B5, etc.; Df(2L)pr21 also called Df(2L)SD-7pr21. deficiency cytology ref ( genetics _______________________________________________________________ Df(2L)pr2b 38B5-C1;38D2-E1 pr- Df(2L)pr8b 38A2-5;39A2-B1 pr- Df(2L)pr21 37E3-F1;38C6-10 2, 3 pr- Df(2L)pr26 37D5-6;38C8-10 2, 3 ref(2)P--pr- Df(2L)pr28 37D3-E1;38C6-9 pr- Df(2L)pr40 38A2-5;38A6-D1 pr- Df(2L)pr47 38B1-2;38C1-2 2 pr- Df(2L)pr49 38B3-6;38C6-10 2 pr- Df(2L)pr65 38A3-5;38D3-5 2 pr- Df(2L)pr67 38A5-8;39C-E 2 pr--l(2)crc- Df(2L)pr69 38B1-2;38C5-6 2 pr- Df(2L)pr76 37D;38E 1 pr- Df(2L)pr-A1 4 pr- Df(2L)pr-A2 4 pr- Df(2L)pr-A3 4 pr- Df(2L)pr-A4 4 pr- Df(2L)pr-A5 4 pr- Df(2L)pr-A6 4 pr- Df(2L)pr-A7 4 pr- Df(2L)pr-A8 36F8-11;38B6-C1 4 Tft--pr- Df(2L)pr-A9 4 pr- Df(2L)pr-A14 37D2-7;39A4-7 3, 4, 7 Sd--pr- Df(2L)pr-A16 37B2-12;38D2-5 3, 4, 7 hk--pr- Df(2L)pr-A20 38A3-4;38B6-C1 4 pr- Df(2L)pr-B5 38A7-8;39A4-C4 4 pr- Df(2L)pr-B10 38A7-8;39A4-C4 4 pr- Df(2L)pr-B11 38A7-8;39A4-C4 4 pr- Df(2L)pr-B12 38A7-8;39A4-C4 4 pr- Df(2L)pr-B14 38A7-8;39A4-C4 4 pr- Df(2L)pr-F59 | 37D;38F 5 ref(2)P--pr- Df(2L)pr-F65 | 5 hk--l(2)crc- Df(2L)pr-F99 | 5 pr- Df(2L)pr-F144 | 5 ref(2)P--l(2)crc- Df(2L)pr-F257 | 5 ref(2)P--l(2)crc- Df(2L)pr-F280 | 5 ref(2)P--l(2)crc- Df(2L)pr-F286 | 5 hk--l(2)crc- Df(2L)pr-R 37D1;38C1 6 pr- ( 1 = Ashburner, Faithfull, Littlewood, Richards, Smith, Vel- issariou, and Woodruff, 1980, DIS 55: 193-195; 2 = Brittnacher and Ganetzky, 1983, Genetics 103: 659-73; 3 = Gay and Contamine; 4 = Ganetzky, 1977, Genetics 86: 321-55; 5 = Nakamura, 1973, Thesis, Paris-Sud; 6 = Roberts, 1971, DIS 46: 122; 7 = T.R.F. Wright. | Derived from Dp(2;Y)G. # Df(2L)PR7F cytology: In 2L heterochromatin just distal to the centromere. discoverer: Hilliker. references: Brittnacher and Ganetzky, 1984, Genetics 107: 423-34. # Df(2L)prd1.25: Deficiency (2L) paired cytology: Df(2L)33B6-7;33E1-2 + T(Y;2)21;40. discoverer: Nusslein-Volhard. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. Nusslein-Volhard, Kluding, and Jurgens, 1985, Cold Spring Har- bor Symp. Quant. Biol. 50: 145-54. genetics: Deficient for prd. # Df(2L)prd1.7 location: Df(2L)33B2-3;34A1-2. discoverer: Nusslein-Volhard. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. Nusslein-Volhard, Kluding, and Jurgens, 1985, Cold Spring Har- bor Symp. Quant. Biol. 50: 145-54. genetics: Deficient for prd. molecular biology: Distal breakpoint mapped to the DNA (Frei, Baumgartner, Edstrom, and Noll, 1985, EMBO J. 4: 979-87). # Df(2L)prd2.27: see Tp(2;3)prd2.27 # Df(2L)prd5.12: see Tp(2;Y)prd5.12 # Df(2L)Prl: Deficiency (2L) Proxless cytology: Df(2L)32F1-3;33F1-2 (Ashburner). discoverer: B.S. Baker. references: Jurgens, 1988, EMBO J. 7: 189-96. Frei, Schuh, Baumgartner, Burri, Noll, Jurgens, Seifert, Nauber, and Jackle, 1988, EMBO J. 7: 197-204. genetics: Associated with Prl. Deficient for prd, sal (Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82), and nub but not b (Ash- burner). molecular biology: Distal breakpoint mapped to the DNA at about -430 to -400 kb (Frei et al., 1988). # Df(2L)prx origin: X ray induced. discoverer: Simpson. deficiency cytology genetics _______________________________________________ Df(2L)prx3 35D3;35D4 ( sna--l(2)35Dd- Df(2L)prx13 35D1;35D4 l(2)35Ce--l(2)35Dg- Df(2L)prx18 not visible Df(2L)prx19 35C1;35D1-2 l(2)35Cb--l(2)35Dd- Df(2L)prx24 35B3-35E1-2 l(2)35Bb--l(2)35Dg- Df(2L)prx31 35D1;35D4 rd--l(2)35Dg- ( Probably not detectable. # Df(2L)rd9: Deficiency (2L) reduced cytology: Df(2L)35A4;35B3. origin: / ray induced. discoverer: Thompson. genetics: Deficient for noc-Adh. # Df(2L)RMD: Deficiency (2L) Roy Manna Duttagupta cytology: Not visible. origin: X ray induced. references: Roy, Manna, and Duttagupta, 1984, J. Biosci. 6: 87-95. deficiency synonym genetics ( ______________________________________________ Df(2L)RMD42 l(2)42 l(2)24EFa--l(2)24EFd- Df(2L)RMD113 l(2)113 l(2)24EFc--l(2)24EFd- Df(2L)RMD149 l(2)149 l(2)24EFb--l(2)24EFd- Df(2L)RMD202 l(2)202 l(2)24EFa--l(2)24EFc- Df(2L)RMD239 l(2)239 l(2)24EFb--l(2)24EFc- Df(2L)RMD261 l(2)261 l(2)24EFa--l(2)24EFc- Df(2L)RMD269 l(2)269 l(2)24EFa--l(2)24EFg- M24F-dw24F-dp- ( Order of loci unknown. # Df(2L)S: Deficiency (2L) Star origin: X ray induced. discoverer: E.B. Lewis, 1940. references: 1945, Genetics 30: 147-51. deficiency cytology genetics _________________________________________ *Df(2L)S1 21C3-4;22A2-3 ds--ast- Df(2L)S2 21C6-D1;22A6-B1 ds--shr- Df(2L)S3 ( 21D2-3;21F2-22A1 S--ast- *Df(2L)S4 21C3-4;22B2-3 ds--shr- *Df(2L)S5 21C2-3;22A3-4 ex--ast- *Df(2L)S7 21C3-4;21F2-22A1 ds--ast- ( Uncovers ninaA. # Df(2L)S56f: see In(2LR)S56f # Df(2L)S1 (of Simpson): see Df(2L)SS1 #*Df(2L)S-der: Deficiency (2L) Star derived cytology: Df(2L)21D4-E1;21E2-3. new order: Y|21D4 - 21A; 60 - 21E3|101. origin: Synthetic; a combination of YP2D from T(Y;2)21E = T(Y;2)21D4-E1 and 2P4D from T(2;4)astv = T(2;4)21E2-3;101. discoverer: E. B. Lewis. references: 1945, Genetics 30: 137-66. genetics: Deficient for S and ast. Homozygous lethal. # Df(2L)sc19: Deficiency (2L) scute19 origin: X ray induced loss of y+ from Tp(1;2)sc19. references: Semeshin and Szidonya, 1985, DIS 61: 148-54. Szidonya and Reuter, 1988a, DIS 67: 77-79. 1988b, Genet. Res. 51: 197-208. deficiency cytology genetics ( ______________________________________________________ Df(2L)sc19-1 24D5-6;25C8 ed--l(2)25- Df(2L)sc19-3 24E3;25A6-7 dw24F--l(2)25Aa- Df(2L)sc19-4 25A5;25E4-5 slf--mid- Df(2L)sc19-5 25A5;25D6 slf--l(2)25Dd- Df(2L)sc19-6 24F1-2;25C5 l(2)24Ec--l(2)25Ce- Df(2L)sc19-7 24D2-4;25C2-3 ed--l(2)25Cc- Df(2L)sc19-8 24C2-8;25C2-8 ed--l(2)25- Df(2L)sc19-9 24D4-5;25F4-26A1 Df(2L)sc19-10 25A4-5;25B9-C1 slf--l(2)25Be- Df(2L)sc19-11 24D2-4;25B2-4 ed--l(2)25Ac- Df(2L)sc19-12 24A4-5;26A6-B1 slf--l(2)26Aa- Df(2L)sc19-13 24E2-4;25B2-5 dw24F--l(2)25Ba- ( Includes complementation groups localized in the deleted regions by Szidonya (unpublished). # In(2L)Scorv: Inversion (2L) Scutoid - revertant origin: X ray induced reversions of Sco in Tp(2;2)Sco. 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. inversion cytology genetics ____________________________________________________________ In(2L)Scorv2 35D1-2;36D3 includes noc-l(2)35Cb; homozygous lethal In(2L)Scorv4 ( six breaks noc--l(2)35Cb- *In(2L)Scorv5 | 35D1-2;38A3-8 In(2L)Scorv8 34C1-2;35D1-2 homozygous lethal as pharate adults; lethal with Sco In(2L)Scorv11 / 24C3-9;35D1-2 homozygous semi- lethal as pharate adults; escapers extreme Sco In(2L)Scorv17 / 25D3-7;35D1-2 homozygous lethal In(2L)Scorv21 35D1-2;36E1-2 homozygous semi- viable and Sco In(2L)Scorv24 34B1-2;35D1-2 homozygous lethal In(2L)Scorv26 ` 35D1-2;40 semilethal with snaHG31 ( Deletion of 35B1-35D inferred from genetic evidence. new order: 21 - 28F1|33A2 - 35A4|28F5 - 32F4| 37A2 - 38F6|35D2 - 36F11|39A2 - 60. Tentative according to Ashburner and Harrington, 1984. synonym: Df(2L)Sco-rv4. Left break mapped to the DNA (McGill, Chia, Karp, and Ashburner, 1988, Genetics 119: 641-61). | Induced with T(Y;2)CA13 and In(2LR)CA14. / Right break mapped to the DNA (McGill, Chia, Karp, and Ash- burner, 1988, Genetics 119: 647-61). ` Heterochromatic break in 40 assumed on basis of inability to recover autosynaptic derivatives. # Df(2L)Sco1-DV7 cytology: Resembles In(2LR)Scorv1 (Ashburner). origin: / ray induced in In(2LR)Scorv1. discoverer: G. Johnson. genetics: Deficient for sna - l(2)35De. # Df(2L)Sd: Deficiency (2L) Segregation distorter origin: X ray induced. deficiency cytology chromosomal ref ( genetics origin _________________________________________________________________ Df(2L)Sd2 37D1-2;38D2-E1 SD-Roma 1 Sd--ms(2)-; Df(2L)Sd14 37D1-2;38C1-2 SD-Roma 1 Sd--pr- Df(2L)Sd37 37D2-7;38A6-B2 SD-5 1, 2, Sd--ref(2)P- 3, 4 pr+ Df(2L)Sd57 | 37D1-2;38C1-2 SD-Roma 1, 4 l(2)37Cf--pr- Df(2L)Sd68 / 37B3-7;38E3-5 SD-Mad 1 hk--ms(2)38C- Df(2L)Sd77 ` 37D1-2;38C1-2 SD-Mad 1, 4 fs(2)TW1--pr- ( 1 = Brittnacher and Ganetzky, 1983, Genetics 103: 659-73; 2 = Ganetzky, 1977, Genetics 86: 321-55; 3 = Gay and Con- tamine; 4 = T.R.F. Wright. | Distal breakpoint +38.55 - +40.55 kb [for coordinates see deficiency map under l(2)37]. / Deficiency able to generate cad gene transcripts (Macdonald and Struhl, 1986, Nature 324: 537-45). ` Distal breakpoint +47.05 - +52.55 kb [for coordinates see deficiency map under l(2)37]. # Df(2L)SD-7pr21: see Df(2L)pr21 # Df(2L)SD-Mad-d77: see Df(2L)Sd77 # Df(2L)SD-R-m57: see Df(2L)Sd57 # Df(2L)sna-S1: see Df(2L)SS1 # Df(2L)spd: Deficiency (2L) spade cytology: Df(2L)27D-E;28C. discoverer: E.H. Grell. genetics: Deficient for spd. # Df(2L)SS1 cytology: Not visibly deficient. discoverer: Simpson. origin: X ray induced. synonym: Df(2L)sna-S1; Df(2L)S1 (of Simpson). references: Grau, Carteret, and Simpson, 1984, Genetics 108: 347-60. genetics: Deficient for rd - l(2)35Dg (Ashburner). # Df(2L)Su(Pc): Deficiency (2L) Suppressor of Polycomb cytology: Df(2L)37D2-E1;38A8-C1. origin: / ray induced. discoverer: Kennison. references: Kennison and Russell, 1987, Genetics 116: 75-86. genetics: Dominant suppressor of Pc. # Df(2L)Sw-L: Deficiency (2L) Swedish-L cytology: Tip of 2L contains deficiency. origin: Naturally occurring condition in some Swedish strains. discoverer: Gustafson, 1937. genetics: No phenotypic effect. # Df(2L)T317 cytology: Breakpoints unknown; associated with a T(2;4) (Ste- ward and Nusslein-Volhard). references: Steward and Nusslein-Volhard, 1986, Genetics 113: 665-78. genetics: Deficient for dl, l(2)36Bd-ninaD but not M(2)36F. Lethal over Df(2L)H20, Df(2L)H68, Df(2L)TW119, Df(2L)TW137, Df(2L)M36F-S5, Df(2L)VA18, and Df(2L)201. # Df(2L)TE21A cytology: Df(2L)21A;21B4-6; extra bands that fail to pair with normal homologue inserted (Kennison). origin: / ray induced in TE21A. discoverer: Ising. synonym: Df(2L)TE75. references: Ising and Block, 1980, Cold Spring Harbor Symp. Quant. Biol. 45: 527-44. genetics: w+rst+ inserted in 21B with loss of terminal bands of 2L [l(2)gl-net-l(2)-al+]; proximal to breakpoint of In(2L)shv54 = In(2L)21B6-C1;22F1-2. # In(2L)TE35A: Inversion (2L) Transposing Element origin: / ray induced. synonym: In(2L)TE146Z. inversion cytology discov ( ref | genetics _______________________________________________________________________ In(2L)TE35A-1 35B;39A-B 1 1 In(2L)TE35A-3 35B1;40 1 In(2L)TE35A-8 35B1-2;35C4 2 1 In(2L)TE35A-9 35B1-2;40 1 1 variegates for w+ In(2L)TE35A-11 35B1-2;40 2 1 variegates for w+ In(2L)TE35A-13 35B1-2;40 + Df 1 1, 2 pu--l(2)35Dg- In(2L)TE35A-16 35B1-2;40 2 In(2L)TE35A-27 35B1-2;38C1-2 2 1 In(2L)TE35A-53 35B1-2;40 4 1 In(2L)TE35A-55 35B1-2;36C3-11 4 1 In(2L)TE35A-56 35B1-2;40 4 1 In(2L)TE35A-63 35B1-2;40 In(2L)TE35A-210 28B12-D1-2;35B 3 1 In(2L)TE35A-220 35B;39D 3 1 In(2L)TE35A-225 35B;40 3 1 In(2L)TE35A-227 40;72B-C + 1 In(2L)35B;40 + In(3R)81;88B ( 1 = Durrant; 2 = Roote; 3 = Samkange; 4 = Wilkins. | 1 = Ashburner; 2 = Gubb, Roote, Harrington, Durrant, Shel- ton, and Ashburner, 1985, Chromosoma 92: 116-23. # Df(2L)TE35BC origin: / ray induced in TE35BC. synonym: Df(2L)TE36. genetics: Deficient for w and rst except for Df(2L)TE35BC-23, Df(2L)TE35BC-28, and Df(2L)TE35BC-31, which have remnants of the bands in TE35BC and carry rst+. deficiency cytology discov ref ( genetics _________________________________________________________________________ Df(2L)TE35BC-1 35C1;35D1 Gubb 1, 2, 3 Su(H)--ck-;vasa+ Df(2L)TE35BC-3 35C1;35D2 Gubb 1, 3 ck--lace- Df(2L)TE35BC-4 35B4;35C3 Gubb 1, 3 l(2)35Bb--dgl- Df(2L)TE35BC-6 34D3-6;35C1 Gubb 3 l(2)34Db--l(2)35Cb- Df(2L)TE35BC-7 | 35B3; Gubb 3 noc--ck-;vasa+ 35B9-10 Df(2L)TE35BC-8 35B1-2; Gubb 3 el--l(2)35Dg- 35E1-2 Df(2L)TE35BC-23 34D1-2; Shelton 3 l(2)34Db--ck- 35B10-C1 Df(2L)TE35BC-24 34B4-6; Shelton 3 l(2)35Bg--l(2)35Ea- 35E1-2 Df(2L)TE35BC-28 35B2;35B7 Shelton 3 l(2)35Bb--ck- Df(2L)TE35BC-29 / 35A3;35C1 Shelton 3 wb--vasa- Df(2L)TE35BC-31 34F5;35B10 Shelton 3 wb--ck- Df(2L)TE35BC-34 35B4;35D4 Shelton 3 l(2)35Bb--l(2)35Dd- Df(2L)TE35BC-35 35B2;35D4 Shelton 3 l(2)35Bb--lace- ( 1 = Ashburner, 1982, Genetics 101: 447-59; 2 = Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91; 3 = Gubb, Shelton, Roote, McGill, and Ashburner, 1984, Chro- mosoma 91: 54-64. | Molecular biology: Left breakpoint mapped to the DNA at -70 kb (Chia, Karp, McGill, and Ashburner, 1985, J. Mol. Biol. 186: 689-706). / Left breakpoint mapped to the DNA between -3 and -2 kb (Lasko and Ashburner, 1988, Nature 335: 611-17). # Df(2L)TE36A origin: / ray induced in TE36A. synonym: Df(2L)TE116. references: Lasko and Ashburner, 1988, Nature (London) 335: 611-17. deficiency cytology genetics molecular biology ( ________________________________________________________________________ Df(2L)TE35D-4 35C1-2;? l(2)35Cb- +15.5 to +18.5 kb Df(2L)TE35D-16 35B9-C1;? vas- to l(2)35Cb- -5.1 to -3.7 kb (circa) Df(2L)TE35D-18 35B9-C1;? vas- to l(2)35Cb- -5.1 to -3.8 kb (circa) ( DNA coordinates for the distal breakpoints of the deficien- cies (0 point is the EcoRI site immediately proximal to the starting point of the walk; "+" values to right, "-" values to left). #*Df(2L)TE37C-1 cytology: Df(2L)37C2-5;38F5-39A1 (broken within the transposition). origin: / ray induced in TE37C. synonym: Df(2L)TE42-1. references: Marsh and Wright, 1979, Genetics 92: s74-75. Wright, Beerman, Marsh, Bishop, Steward, Black, Tomsett, and Wright, 1981, Chromosoma 83: 45-58. genetics: w+ but not rst+ deleted. Deficient for l(2)37Cf-Bl. # Df(2L)TE38A-1 cytology: Df(2L)38A6-7;38B6-C1. origin: / ray induced in TE38A. synonym: Df(2L)TE48-1. discoverer: Robertson. references: T.R.F. Wright. genetics: Deficient for pr and TE38A. Lethal over Df(2L)TW150, but viable over Df(2L)TW130. # Df(2L)TE38A-2 cytology: Df(2L)37F6-38A1;40. origin: / ray induced in TE38A of Ising. synonym: Df(2L)TE48-2. discoverer: T.R.F. Wright. genetics: Deficient for pr, M(2)39F, and TE38A of Ising. Lethal over Df(2L)TW150, but viable over Df(2L)TW130. # Df(2L)TE42: see Df(2L)TE37C #*Df(2L)TE48: see Df(2L)TE38A # Df(2L)TE146: see Df(2L)TE35A # Df(2L)tkv2: Deficiency (2L) thick veins cytology: Df(2L)25D2-5;25D6-E1. origin: X ray induced. discoverer: Szidonya. synonym: Df(2L)tkv-Sz2. references: Reuter and Szidonya, 1983, Chromosoma 88: 277-85. Szidonya and Reuter, 1988a, DIS 67: 77-79. 1988b, Genet. Res. 51: 197-208. genetics: Deficient for tkv-l(2)25De but not for l(2)25Ea. # Df(2L)tkv3 cytology: Df(2L)25A2-3;25D5-E1. origin: X ray induced. discoverer: Szidonya. synonym: Df(2L)tkv-Sz3. references: Reuter and Szidonya, 1983, Chromosoma 88: 277-85. Szidonya and Reuter, 1988a, DIS 67: 77-79. 1988b, Genet. Res. 51: 197-208. genetics: Deficient for slf-tkv. Females sterile; males sem- isterile. # Df(2L)TW: Deficiency (2L) Ted Wright origin: Df(2L)TW1-Df(2L)TW161 are X ray induced, Df(2L)TW201- Df(2L)TW203 are / ray induced, Df(2L)TW330 formaldehyde or ethyl methanesulfonate induced. synonym: Df(2L)1-Df(2L)330. deficiency cytology ref ( genetics _______________________________________________________________________ Df(2L)TW1 | 38A7-B1;39C2-3 5, 8, 10 pr--Bl- crc+ Df(2L)TW2 37D2-E1;38E6-9 3, 8, 10 ref(2)P--Bl- crc+ Df(2L)TW3 / 36F7-37A1;37B2-8 1, 7, 8, 10 Tft--Roi- hk+ Df(2L)TW9 37E2-F4;38A6-B1 3, 8, 10 Bl+ ref(2)P--pr- Df(2L)TW12 37E2-F4;39D1-2 5, 8, 10 ref(2)P+ pr--crc- Df(2L)TW50 ` 36E4-F1;38A6-7 1, 8, 10 rdo+ M(2)36F- -ref(2)P- pr+ Df(2L)TW65 37F5-38A1;39E2-F1 3, 4, 5, 8, 10 pr--His- Df(2L)TW68 not confirmed 10 bD and strong M Df(2L)TW84 37F5-38A1;39D3-E1 3, 4, 5, 8, 10 ref(2)P+ pr--His- (partial) Df(2L)TW119 ` 8, 10 dl--rdo- M(2)36F+ Df(2L)TW130 - 37B9-C1;37D1-2 2, 9, 10 hk--fs(2)TW1- Df(2L)TW137 ` 36C2-4;37B9-C1 1, 8, 10 dl--msl-1- hk+ Df(2L)TW150 37F5-38A1;38B2-C1 3, 8, 10 ref(2)P+ l(2)37Fd- -l(2)A113- Df(2L)TW158 37B2-8;37E2-F4 1, 3, 6, 8, 10 msl-1+ hk- -l(2)37Ea- ref(2)P+ Df(2L)TW161 38A6-B1;40A4-B1 3, 4, 5, 10 pr--His-; moderate M Df(2L)TW201 36E-F;37A 8 l(2)36Da+ rdo- -Tft- hk+ Df(2L)TW202 ` 36F2-5;37A 8 rdo+ M(2)36F- -Tft- hk+ Df(2L)TW203 n 36E4-F1;37B9-C1 8, 9 l(2)36Da+ rdo- -hk- Df(2L)TW330 ` 36E4-F1;37D1-2 8 l(2)36Da+ rdo- -fs(2)TW1- ( 1 = Belote and Lucchesi, 1980, Genetics 96: 165-86; 2 = Brittnacher and Ganetzky, 1983, Genetics 103: 659-73; 3 = Gay and Contamine; 4 = Moore, Procunier, Cross, and Gri- gliatti, 1979, Nature 282: 312-14; 5 = Moore, Sinclair, and Grigliatti, 1983, Genetics 105: 327-44; 6 = Struhl, 1981, Nature 293: 36-41; 7 = Voelker and Langley, 1978, DIS 53: 185; 8 = T.R.F. Wright; 9 = Wright, Beerman, Marsh, Bishop, Steward, Black, Tomsett, and Wright, 1981, Chromo- soma 83: 45-58; 10 = Wright, Hodgetts, and Sherald, 1976, Genetics 84: 267-85. | Associated with T(2;3)40;65 (Garcia-Bellido, Moscoso del Prado, and Botas, 1983, Mol. Gen. Genet. 192: 253-63). / Associated with, but separable from, T(2;3)53A;99 and In(3L)64C-F;71C (Garcia-Bellido et al., 1983). ` Molecular biology: Distal DNA breakpoints given (Steward, McNally, and Schedl, 1984, Nature 311: 262-65). - Phenotype hk over Df(2L)TW203. Molecular biology: Deletes the entire 100 kb of DNA which carries Ddc and includes the coding region for the genes l(2)37Ba--l(2)37Cf (Gilbert, Hirsh, and Wright, 1984, Genetics 106: 679-94). esc not included in this deficiency (Struhl, 1981). n Induced Tft revertant. Phenotype rdo over Df(2L)TW119, hk over Df(2L)TW130 or Df(2L)VA23. Molecular biology: Proxi- mal breakpoint distal to -59 kb (Ddc coordinates from Gil- bert, Hirsh, and Wright, 1984). # Df(2L)V44: Deficiency (2L) Valencia cytology: Df(2L)29E5;29E6. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-78. # Df(2L)V106 cytology: Df(2L)37B;37B. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. # Df(2L)VA origin: / ray induced [Df(2L)VA1-Df(2L)VA14, Df(2L)VA18]; / ray or ethyl methanesulfonate induced [Df(2L)VA15-Df(2L)VA17, Df(2L)VA19, Df(2L)VA22]; diepoxybutane induced [Df(2L)VA20, Df(2L)VA21, Df(2L)VA23, Df(2L)VA24] or resulting from hybrid dysgenesis with Harwich P [Df(2L)VA25]. mol. deficiency cytology ref ( genetics biol | ________________________________________________________________________ Df(2L)VA1 8 pr-; lethal over Df(2L)TE37C-1 Df(2L)VA2 8 pr-; lethal over Df(2L)TE37C-1 Df(2L)VA3 8 pr-; lethal over Df(2L)TE37C-1 Df(2L)VA4 8 pr-; lethal over Df(2L)TE37C-1 Df(2L)VA5 8 pr-; lethal over Df(2L)TE37C-1 Df(2L)VA6 / 37D2-E1; 3, 9 pr- 38F2-39A1 Df(2L)VA7 9 pr-; lethal over Df(2L)TE37C-1 Df(2L)VA8 37D2-3; 3, 9 pr- 38F5-39A1 Df(2L)VA10 6, 8 pr-; lethal over Df(2L)TE37C-1 Df(2L)VA11 6, 8 pr-; lethal over DF(2L)TE37C-1 Df(2L)VA12 37C2-5; 7, 8, 10 Ddc+ l(2)37Cf-- pr- 1 38B2-C1 Df(2L)VA13 37C2-5; 1, 8, 10 Ddc+ l(2)37Cf-- pr- 2 38C2-D1 Df(2L)VA14 3, 7, 8 hk-- l(2)37Cf- l(2L)37Db+ Df(2L)VA15 2, 8 hk-- l(2)37Db- Df(2L)VA16 3, 4, 8 M(2)36F+ hk-- fs(2)TW1- l(2)37Db+ Df(2L)VA17 37B9-C1; 5, 8, 10 amd+ Ddc-- fs(2)TW1- 3 37F5-38A1 Df(2L)VA18 36C4-D1; 5, 8 dl+ l(2)36Da-- Ddc- 4 37C2-5 l(2)37Ca+ Df(2L)VA19 37C2-D1; 8 l(2)37Cf- 5 38A6-B1 Df(2L)VA20 37B2-8; 3, 4, 8 hk-- fs(2)TW1- 37D2-E1 Df(2L)VA21 36D1-F1; 4, 8 dl+ l(2)36Da-- l(2)37Cg- 6 37C2-D1 fs(2)TW1+ Df(2L)VA22 {36E4-F1; 8 l(2)36Da+ rdo-- l(2)37Cf- 37D2-E1} l(2)37Db+ Df(2L)VA23 ` 37B9-C1; 4, 8 hk-- l(2)37Db- 37D2-E1 Df(2L)VA24 4, 8 hk-- l(2)37Ea- Df(2L)VA25 - 4, 8 M(2)36F+ hk-- fs(2)TW1- ( 1 = Bishop; 2 = Black; 3 = Brittnacher and Ganetzky, 1983, Genetics 103: 659-73; 4 = Cecil; 5 = Cecil and Wade; 6 = Steward; 7 = Tomsett; 8 = T.R.F Wright; 9 = T.R.F. Wright and E.Y. Wright; 10= Wright, Beerman, Marsh, Bishop, Steward, Black, Tomsett, and Wright, 1981, Chromosoma 83: 45-58. | Ddc DNA coordinates from Gilbert, Hirsh, and Wright, 1984, Genetics 106: 679-84: 1 = Distal breakpoint between +25.5 and +28.1 kb; 2 = Distal breakpoint between +30.8 and +35 kb; 3 = Distal breakpoint within the Ddc gene between +1.4 and 2.4 kb removing the first 5' exon; 4 = Proximal break- point between +5.1 and +5.6 kb; 5 = Distal breakpoint between +30 and +32 kb (E.S. Pentz); 6 = Proximal breakpoint between +27 and +30 kb (E.S. Pentz). / Viable over Df(2L)VA25 but with wings held down and out. ` Viable over Df(2L)TW203 but shows hk phenotype. - Wings held outstretched when over l(2)37Db and held down and outward when over Df(2L)VA6. # Df(2L)VV5 cytology: Df(2L)22A3;22E4. origin: X ray induced. discoverer: Velissariou. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. # Df(2L)VV9 cytology: Df(2L)30B3;30C9. origin: / ray induced. discoverer: Velissariou. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. # Df(2L)W cytology: Df(2L)35A2-3;35B3-5. origin: Spontaneous in natural population (Greece). synonym: l(2)AR8. references: Woodruff and Ashburner, 1979, Genetics 92: 117-32. genetics: Deficient for l(2)34Fa-Adh. # Df(2L)X1: see Df(2L)L138D # Df(2L)X14: see Df(2L)L138D # Df(2L)XR: see Df(2L)L138D # Df(2R)017 cytology: Df(2R)56F5;56F15. origin: Induced by ethyl methanesulfonate. references: Duttagupta and Shellenbarger, 1980, Development and Neurobiology of Drosophila (Siddiqi, Babu, Hall, and Hall, eds.). Plenum Press, New York and London, pp. 25-33. genetics: Includes l(2)56Fd, l(2)56Fe, l(2)56Ff, and l(2)56Fg. # Df(2R)2J: see Df(2R)A'' # Df(2R)6C: see Df(2R)A'' # Df(2R)7B: see Df(2R)Pcl7B # Df(2R)10G: see Df(2R)A'' # Df(2R)11B: see Df(2R)Pcl11B # Df(2R)14C: see Df(2R)A'' # Df(2R)42 cytology: Df(2R)42C3-8;42D2-3. origin: Probably X ray induced. Found on chromosome with vgS. discoverer: Bridges, 36b. references: Morgan, Bridges, and Schultz, 1938, Year Book - Carnegie Inst. Washington 37: 304-9. genetics: Deficient for no tested loci. Homozygous lethal. # Df(2R)43A cytology: Df(2R)43A2;43B1. # Df(2R)44CE cytology: Df(2R)44C;44E1-4. discoverer: Yannopoulos. references: Hooper and Scott, 1989, Cell 59: 751-65. genetics: Deficient for tuf. # Df(2R)173 cytology: Not visible. origin: Induced by ethyl methanesulfonate. references: Duttagupta and Shellenbarger, 1980, Development and Neurobiology of Drosophila (Siddiqi, Babu, Hall, and Hall, eds.). Plenum Press, New York and London, pp. 25-33. genetics: Includes l(2)56Fa, l(2)56Fb, and M(2)56F. # Df(2R)193A cytology: Df(2R)44C;44C. # Df(2R)A cytology: Deficient for about half of the 2R heterochromatin including rl (Hilliker, 1976). origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes (Hilliker and Holm, 1975). references: Hilliker and Holm, 1975, Genetics 81: 705-21. Hilliker, 1976, Genetics 83: 765-82. genetics: Deficient for rl. Complements Df(2R)M41A4 and Df(2R)M41A8 but not Df(2R)M41A10 (Hilliker, 1976). other information: Thirty-three such deficiencies recovered. # Df(2R)A' cytology: Deficient for most of the 2R heterochromatin includ- ing rl. Extends distal to Df(2R)A and Df(2R)A'' (Hilliker, 1976). origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes (Hilliker and Holm, 1975). references: Hilliker and Holm, 1975, Genetics 81: 705-21. Hilliker, 1976, Genetics 83: 765-82. genetics: Deficient for rl and M(2)41A. Lethal over Df(2R)M41A4, Df(2R)M41A8, and Df(2R)M41A10 (Hilliker, 1976). # Df(2R)A'' cytology: Df(2R)41 (heterochromatin). Deficient for about two- thirds of the 2R heterochromatin including rl. Extends distal to Df(2R)A (Hilliker, 1976). origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes (Hilliker and Holm, 1975). references: Hilliker, 1976, Genetics 83: 765-82. Ganetzky, 1977, Genetics 86: 321-55. genetics: Deficient for rl. Complements Df(2R)M41A4 and Df(2R)M41A8 but not Df(2R)M41A10 (Hilliker, 1976). #*Df(2R)a-ba2: Deficiency (2R) arc-broad angular cytology: Df(2R)58D5-6;58D7-8. origin: Spontaneous. discoverer: Goldschmidt. references: 1945, Univ. Calif. (Berkeley) Publ. Zool. 49: 363-73, 388-89. genetics: Associated with aba2. # Df(2R)AA21: see In(2R)AA21 # Df(2R)B cytology: Deficient for less than half of the 2R heterochroma- tin not including rl (Hilliker, 1976). origin: /-ray-induced reconstitution of chromosome 2 by detach- ment of compound second chromosomes (Hilliker and Holm, 1975). references: Hilliker and Holm, 1975, Genetics 81: 705-21. Hilliker, 1976, Genetics 83: 765-82. genetics: Not deficient for rl. Complements Df(2R)M41A4 and Df(2R)M41A8 but not Df(2R)M41A10. # Df(2R)Ba cytology: Df(2R)60E3;60E6 origin: / ray induced. discoverer: Moscoso del Prado. synonym: Art2, BaMP. references: Sunkel and Whittle, 1987, Wilhelm Roux's Arch. Dev. Biol. 196: 124-32. Cohen, Bronner, Kuttner, Jurgens, and Jackle, 1989, Nature 338: 432-34. Cohen and Jurgens, 1989, EMBO J. 8: 2045-55. genetics: Deficient for Ba; entire putative transcription unit deleted. Heterozygote shows partial transformation of aristae to tarsal segments. Dominant phenotype suppressed in either Pcl10 or Df(2R)en28 heterozygotes. Df(2R)Ba/+ shows almost complete suppression of the extra-sex combs phenotypes of Pc4/+, PcT7/+, Pcl10/+, Pcl11/+, AntpScx/+, Msc/+, and MscT3/+. molecular biology: Deleted for the region from approximately coordinate 90 kb through 180 kb and beyond on the molecular map of Cohen et al. # Df(2R)Ba4: Deficiency (2R) Brista cytology: Df(2R)60D1-2;60F5. origin: EMS-induced. references: Sunkel, 1983, Ph.D. Thesis, University of Sussex. genetics: Deficient from sp to 2R tip. Heterozygotes have missing legs, and abnormal eye facets. Lethal over Ba. # Df(2R)Ba-MP (J. Kennison) cytology: Df(2R)60E3-4;60E5-6. origin: X ray induced. discoverer: Moscoso del Prado. synonym: ScnpA1; Art2; DllMP. genetics: Recessive lethal. Heterozygotes show partial transformation of arista to tarsal segments. molecular biology: Deletion removes the entire Ba coding region [Cohen, Bronner, Kuttner, Jurgens, and Jackle, 1989, Nature (London), 338: 432-34]. # Df(2R)BP7 cytology: Df(2R)57E;58A1. origin: Constructed from T(2;3)P49 = T(2;3)57D;81F and T(2;3)BTD73 = T(2;3)58A1;81F. references: Schejter, and Shilo, 1989, Cell 56: 1093-1104. genetics: Does not complement lethal mutations of Egfr. # Df(2R)bwALCyR: see In(2R)bwALCyR # Df(2R)bwVDe1LCyR: see In(2R)bwVDe1LCyR # Df(2R)bwVDe2LCyR: see In(2R)bwVDe2LCyR # Df(2R)bw5: Deficiency (2R) brown cytology: Df(2R)59D10-E1;59E4-F1. origin: Spontaneous. discoverer: Mohr, 31k28. references: Wright, 1970, Advances in Genetics 15: 262-85. genetics: Deficient for bw. Homozygous lethal in embryo (Tsai, 1955, Genetics 40: 601). # Df(2R)bw-D23 cytology: Df(2R)59D4-5;60A1-2 (Richards). origin: X ray induced. synonym: Df(2R)bwDrv23; Df(2R)bwD+R23. references: Simpson, 1983, Genetics 105: 615-32. genetics: Deficient for bw but not for twi. # Df(2R)bw-D31 cytology: Df(3R)59B6-8;60A8-16 (Richards). origin: X ray induced. synonym: Df(2R)bwDrv31;Df(2R)bwD+R31. references: Simpson, 1983, Genetics 105: 615-32. genetics: Deficient for bw and twi. # Df(2R)bw-GY cytology: Df(2R)59B;59E. origin: Recovered as apparent recombinant from a test cross of a dysgenic-type male that was heterozygous for a maternally derived dp b cn bw second chromosome and paternally derived autosome extracted from a natural population and capable of promoting male recombination. An MRF (Male Recombination Fac- tor) chromosome, MRF23.5, was utilized. The duplication was recovered from a male heterozygous for MRF23.5. references: Yannopoulos, Stamatis, Zacharopoulou, and Pelecanos, 1981, Mutat. Res. 83: 383-93. genetics: Deficient for bw. # Df(2R)bw-K cytology: Df(2R)59D2-5;59E1-3. origin: Spontaneous. references: Koliantz, 1971, DIS 46: 52. genetics: Deficient for bw. #*Df(2R)bw-R40: Deficiency (2R) brown-Rearranged cytology: Df(2R)59C5-6;59E2-3. origin: X ray induced. discoverer: Slatis. references: 1955, Genetics 40: 5-23. # Df(2R)bw-S46 cytology: Df(3R)59D8-11;60A7 (Richards). origin: X ray induced. references: Simpson, 1983, Genetics 105: 615-32. genetics: Deficient for bw but not twi. # Df(2R)C113 cytology: Df(2R)41A;41A. references: Tano, 1966, Jpn. J. Genet. 41: 299-308. genetics: Deficient for l(2)41Ae. Complemented by M(2)41A and M(2)39F but not by Df(2R)rl10A. # Df(2R)CA53 cytology: Df(2R)43E6;44B5-9. origin: / ray induced. discoverer: Durrant. genetics: Deficient for cn. Ocelli small in heterozygotes. # Df(2R)CA58 cytology: Df(3R)43A3;43F6. origin: / ray induced. discoverer: Ashburner. # Df(2R)CC2 cytology: Df(2R)57C3;57C6. origin: / ray induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Deficient for l(2)57Cb-Pu. # Df(2R)cn: Deficiency (2R) cinnabar origin: Most deficiencies recovered as apparent cn double recombinants from test crosses of dysgenic-type males that were heterozygous for a maternally derived dp b cn bw second chromosome and paternally derived autosomes extracted from natural populations and capable of promoting male recombina- tion. Rearranged derivatives occurred both singly and in clusters. Two MRF (Male Recombination Factor) chromosomes, MRF23.5 and MRF31.1, were utilized. Most deficiencies of MRF origin were recovered from males heterozygous for MRF23.5; 1b and 2b recovered from males heterozygous for MRF31.1. deficiency cytology origin ref ( __________________________________________________ Df(2R)cn1 42E;44A MRF 3 Df(2R)cn1b 43D;44B 1 Df(2R)cn2 42E;43F MRF 3 Df(2R)cn2b 42B;43E 1 Df(2R)cn3 42E;44B MRF 3 Df(2R)cn4 43D;44C MRF 3 Df(2R)cn5 43E;43E MRF 3 Df(2R)cn6 43D;43E MRF 3 Df(2R)cn7 43D;44C + MRF 3 In(2R)47C;54B Df(2R)cn8 43C;44B MRF 3 Df(2R)cn9 42E;44C MRF 3 Df(2R)cn10 43C;44C + MRF 3 In(2R)44A;54B Df(2R)cn11 43E;43E MRF 3 Df(2R)cn12 43E;43F MRF 3 Df(2R)cn13 43D;43E + MRF 3 In(2R)50F;54B Df(2R)cn14 43E + In(3R)37C;59C MRF 3 Df(2R)cn15 42E;43F MRF 3 Df(2R)cn16 42E;43E MRF 3 Df(2R)cn17 43C;44B + MRF 3 T(2;3)57C;69E Df(2R)cn18 43E;44B + MRF 3 In(2R)43B;54A Df(2R)cn19 43E;43F + MRF 3 In(2R)57C;59C Df(2R)cn20 43D;44C MRF 3 Df(2R)cn21 43E;43F MRF 3 Df(2R)cn81 43D1-7;44A3-7 / ray 2 Df(2R)cn83c 43C5-D1;44B6-C1 1 Df(2R)cn87a 42B4-C1;43F-44A1 1 Df(2R)cn87e 42B4-C1;43F-44A1 1 Df(2R)cn88b 42A;42E 1 Df(2R)cn-h1 43B1-C1;43E6-15 1 Df(2R)cn-h2 43D2-43E3;43E15-F1 1 Df(2R)cn-h3 43C1-D1;43E15-F1 1 ( 1 = Ashburner; 2 = Gubb 81i1; 3 = Yannopoulos, Stamatis, Zacharopoulou, and Pelecanos, 1981, Mutat. Res. 83: 383-93. # Df(2R)Cy-sf: Deficiency (2R) Curly-safranin origin: X ray induced. references: Davis and MacIntyre, 1988, Genetics 120: 755-66. genetics: Deficient for sf. # Df(2R)CyLbwVDe1R: see In(2R)CyLbwVDe1R # Df(2R)CyLbwVDe2R: see In(2R)CyLbwVDe2R # Df(2R)D17 cytology: Df(2R)57B5;58B1-2. discoverer: O'Donnell. references: Schupbach and Wieschaus, 1986, Wilhelm Roux's Arch. Dev. Biol. 195: 302-17. O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Deficient for tud (Schupbach and Wieschaus, 1980), and Pu (O'Donnell et al., 1989). # Df(2R)Egfr: Deficiency (2R) Epidermal growth factor references: Price, Clifford, and Schupbach, 1989, Cell 56: 1085-92. deficiency cytology origin synonym genetics ____________________________________________________________________ Df(2R)Egfr3 57E1;57F11 EMS flb3F18 mat(2)N--Egfr- Df(2R)Egfr5 57D2-8;58D1 / ray Df(2R)top5D mat(2)N--Egfr- Df(2R)Egfr18 57E4-11;57F1 / ray Df(2R)top18A Egfr- # Df(2R)en: Deficiency (2R) engrailed genetics: Deficient for en. Enhance Pc (Sato, Russell, and Denell, 1983, Genetics 105: 357-70). deficiency cytology origin ( discoverer | ref / _________________________________________________________________________ Df(2R)en28 complex; see 1 2 1, 2, 3, 7 In(2R)en28 Df(2R)en30 ` 48A3-4;48C6-8 1 2 1, 2, 3, 5, 7 Df(2R)en-A - 47D3;48A5-6 2 1 2, 3, 4 Df(2R)en-B - 47E3;48B2 2 1 2, 4 Df(2R)en-SFX31 48A1;48B5-7 2 3 5, 6 ( 1 = / rays; 2 = X rays; | 1 = Ashburner; 2 = Eberlein and Russell; 3 = Kornberg. / 1 = Eberlein, 1982, Genetics 100: s21-22; 2 = Eberlein and Russell, 1983, Dev. Biol. 100: 227-37; 3 = Epper and S'nchez, 1983, Dev. Biol. 100: 387-98; 4 = Gubb, 1985, Wilhelm Roux's Arch. Dev. Biol. 194: 236-46; 5 = Kuner, Nakanishi, Ali, Drees, Gustavson, Theis, Kauvar, Kornberg, and O'Farrell, 1985, Cell 42: 309-16; 6 = Kornberg, 1981, Proc. Nat. Acad. Sci. USA 78: 1095-99; 7 = Russell and Eberlein, 1979, Genetics 92: s109. ` Homozygous viable. Left breakpoint between DNA coordinates 13 and 20 kb (Kuner et al., 1985). Claimed to be a viable allele by Kuner et al. despite claimed deficiency and failure to test homozygote by Eberlein and Russell. (Kuner et al., 1985). - Also deficient for shn and sha (Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82). Homozygous lethal extends from coordinate -95 to +115 (Kuner et al., 1985). # Df(2R)ES1 cytology: Distal break at 60F1-2. references: Cote, Preiss, Haller, Schuh, Kienlin, Seifert and Jackle, 1987, EMBO J. 6: 2793-801. genetics: Deficiency for zip-gsb. molecular biology: 60F1-2 break at +54 kb. # Df(2R)eve: Deficiency (2R) even-skipped cytology: Df(2R)46C3-4;46C9-11. discoverer: Nusslein-Volhard. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. Nusslein-Volhard, Kluding, and Jurgens, 1985, Cold Spring Har- bor Symp. Quant. Biol. 50: 145-54. genetics: Deficient for eve. # Df(2R)exu cytology: Df(2R)57A2;57B1. genetics: Deficient for exu. # Df(2R)F4-1 cytology: Df(2R)57A3;57B1-2. genetics: Deficient for exu. # Df(2R)F36 cytology: Df(2R)57B16-17;57C6-7 (Schupbach and Wieschaus, 1986). origin: / ray induced. synonym: Df(2R)Pu-rF36. references: Mackay, Reynolds, and O'Donnell, 1985, Genetics 111: 885-904. Schupbach and Wieschaus, 1986, Wilhelm Roux's Arch. Dev. Biol. 195: 302-17. genetics: Deficient for l(2)57Ba-Pu. GTP cyclohydrolase activity lost in eye but present elsewhere. # Df(2R)gsb: Deficiency (2R) gooseberry cytology: Df(2R)60E9-10;60F1-2. genetics: Deficient for gsb. # Df(2R)IIX62 cytology: Df(2R)60E9-10;60F1-2. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. Cote, Preiss, Haller, Schuh, Kienlin, Seifert, and Jackle, 1987, EMBO J. 6: 2793-2801. genetics: Deficient for gsb and zip. Df(2R)gsb/Df(2R)SB1 embryos express gsb but not zip (Cote et al., 1987). molecular biology: Proximal breakpoint at -55 to -49 kb and distal breakpoint at +40 to +42.5 kb (Cote et al., 1987), with the proximal breakpoint of Df(2R)SB1 approximately at 0. # Df(2R)Jp7 cytology: Df(2R)52F;53A. discoverer: Saxton. references: McDonald and Goldstein, 1990, Cell 61: 991-1000. genetics: Deficient for Kin. # Df(2R)K11 cytology: Df(2R)57C3-4:57D7-8. origin: / ray induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Deficient for Pu. # Df(2R)KL origin: X ray. references: Davis and MacIntyre, 1988, Genetics 120: 755-66. genetics: Deficient for c. deficiency cytology ___________________________ Df(2R)KL9 52D3;52D7-9 Df(2R)KL32 52C5-D1;52E2-5 Df(2R)KL69 52D2-3;52D9-E1 Df(2R)KL99 52B5-C1;52E2-5 # Df(2R)Kr: Deficiency (2R) Kruppel genetics: Deficient for Kr. deficiency synonym cytology origin ref ( ______________________________________________________ Df(2R)Kr1 60F2;60F5 spont 2, 3, 4 Df(2R)Kr4 KrB80 60F2;60F5 X ray 3, 4 Df(2R)Kr6 Kr6A69 60F3;60F5 EMS 3, 4 Df(2R)Kr10 | KrSBl 60E10;60F5 X ray 3 Df(2R)Kr14 KrL14 60F2;60F5 EMS 1, 3 ( 1 = Jurgens, Kluding, Nusslein-Volhard, and Wieschaus, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95; 2 = Nusslein- Volhard and Wieschaus, 1980, Nature 287: 795-801; 3 = Preiss, Rosenberg, Kienlin, Seifert, and Jackle, 1985, Nature 313: 27-32; 4 = Wieschaus, Nusslein-Volhard, and Kluding, 1984, Dev. Biol. 104: 172-86. | Recovered as reversion of If. The deficient region is replaced by transposed bands probably derived from chromo- some 4. # Df(2R)l(2)30 cytology: Df(2R)52D6-7;52A12-B1. origin: Induced by ethyl methanesulfonate. discoverer: Doane. references: Davis and MacIntyre, 1988, Genetics 120: 755-66. genetics: Homozygous lethal. # Df(2R)L4: Deficiency (2R) Lobe cytology: Df(2R)51A2;52A12-B1. origin: X ray induced. synonym: Df(2R)Lrv4;Df(2R)L+R4. references: Baker and Ridge, 1980, Genetics 94: 383-423. genetics: Deficient for L. No complementation of tra-2 for male sterility (Belote and Baker, 1983, Dev. Biol. 95: 512- 17). # Df(2R)L7 cytology: Df(2R)50D;51B5-C2. origin: X ray induced. synonym: Df(2R)Lrv7;Df(2R)L+R7. references: Baker and Ridge, 1980, Genetics 94: 383-423. genetics: Deficient for L. No complementation of tra-2. # Df(2R)L48 cytology: Df(2R)51A1;51B4 (MacIntyre). references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. genetics: Deficient for Asx and L. # Df(2R)M41A: Deficiency (2R) Minute 41A origin: X ray induced. genetics: Homozygous lethal. deficiency cytology synonym ref ( genetics _________________________________________________________________________ Df(2R)M41A salivaries M(2)S2 2, 3, 4 M(2)41A--tk- appear normal Df(2R)M41A4 salivaries M(2)S24 1, 2, 3, l(2)41Ae--ap-; appear 4, 5 includes Dip-A normal Df(2R)M41A8 salivaries M(2)S28 1, 2, l(2)41Ae- appear 3, 5 -stw- ap+ normal Df(2R)M41A10 41A;mitotic M(2)S210 1, 3, l(2)41Aa- 2R 3/4 4, 5 -l(2)41Ah- normal size stw+ Df(2R)M41A50j M(2)S250j 5 rl+ l(2)41Ae- stw+ *Df(2R)M41A-D 41A;41C; *M(2)S2D see *T(Y;2;3)D *Df(2R)M41A-vg11 | M(2)S2vg11 2, 3 rl--msf- ( 1 = Hilliker and Holm, 1975, Genetics 81: 705-21; 2 = Mor- gan, Bridges, and Schultz, 1938, Year Book - Carnegie Inst. Washington 37: 306; 3 = Morgan, Schultz, Bridges, and Curry, 1939, Year Book - Carnegie Inst. Washington 38: 273-77; 4 = Morgan, Schultz, and Curry, 1940, Year Book - Carnegie Inst. Washington 39: 251-55; 5 = Tano, 1966, Jpn. J. Genet. 41: 299-308; 6 = Voelker and Langley, 1978, Genetica 49: 233-36. | Arose simultaneously with vg11. #*Df(2R)M58F cytology: Df(2R)57F11-58A1;58F8-59A1. origin: Spontaneous. discoverer: Bridges, 23g15. synonym: *Df(2R)M-l. references: Morgan, Bridges, and Sturtevant, 1925, Bibliog. Genet. 2: 231. Bridges, 1937, Cytologia (Tokyo), Fujii Jub., Vol. 2: 745-55. genetics: Deficient for px, l(2)Su(H), M(2)58F, and probably a. Homozygote dies in egg stage; eggs recognizable by thin chorion (Li, 1927, Genetics 12: 1-58). # Df(2R)M60E cytology: Df(2R)60E2-3;60E11-12. origin: X ray induced. discoverer: Schultz, 33a7. synonym: Df(2)M-33a; Df(2R)M-c33a; M(2)115. references: Bridges, 1937, Cytologia (Tokyo), Fujii Jub., Vol. 2: 745-55. genetics: Deficient for M(2)60E. Homozygous lethal. Fairly strong M with good viability in combination with Binsn and In(2LR)bwV32g (Campos-Ortega and Waitz, 1978, Wilhelm Roux' Arch. Entwicklungsmech. Org. 184: 155-70). # Df(2R)MP1 cytology: Df(2R)57C1-2;57D1-2. origin: / ray induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. #*Df(2R)Np: Deficiency (2R) Notopleural cytology: Df(2R)44F1-2;45E1-2 (Bridges). origin: Spontaneous. discoverer: Nichols-Skoog, 33b20. references: Bridges, Skoog, and Li, 1936, Genetics 21: 788-95 (fig.). Li, 1936, Peking Nat. Hist. Bull. 11: 39-48. genetics: Not deficient for cn, blo, or en. Df(2R)Np/T(2;3)dp lethal. # Df(2R)Ore-R: Deficiency (2R) Oregon-R cytology: Df(2R)60F2-3;60F5. origin: Naturally occurring in Oregon-R stock but not in Oregon-R-C stock (Roberts, 1974, Genetics 77: s54-55). discoverer: Bridges, 36l5. genetics: No detectable phenotypic effect in homozygote. # Df(2R)P: Deficiency (2R) Pale cytology: Df(2R)58E3-F1;60D14-E2. origin: Aneuploid segregant from Tp(2;3)P/+. # Df(2R)P32 cytology: Df(2R)43A3;43A6 (Sinclair). references: Schupbach, and Wieschaus, 1989, Genetics 121: 101-17. genetics: Uncovers tor, scra, mat(2)cellRE43. # Df(2R)PC4 cytology: Df(2R)55A;55F (Jurgens). references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. Schupbach and Wieschaus, 1986, Wilhelm Roux's Arch. Dev. Biol. 195: 302-17. genetics: Deficient for thr, stau, Pcl (Jurgens, 1985, Nature 316: 153-55); also for Bc, Dox1, fj, and wt (Deng and Rizki, 1988, Proc. Int. Congr. Genet., 16th, p. 192). # Df(2R)PC18 cytology: Df(2R)57B16-17;57C6-7. origin: / ray induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Deficient for l(2)57Ba-Pu. # Df(2R)PC29 cytology: Df(2R)55C1-2;56B1-2. # Df(2R)PC66 cytology: Df(2R)55D2-E1;55E3-4. # Df(2R)Pcl: Deficiency (2R) Polycomblike genetics: Deficient for Pcl. When heterozygous with wild type, flies carrying the Pcl deficiency show transformation of second and third legs to first legs. deficiency cytology discoverer synonym ref ( ___________________________________________________________________ Df(2R)Pcl7B | 54E8-F1;55B9-C1 E. B. Lewis Df(2R)7B 1 Df(2R)Pcl11B | 54F6-55A1;55C1-3 E.B. Lewis Df(2R)11B 1,2 Df(2R)Pcl-W5 55A-B;55C J. Williams 2 ( 1 = Duncan, 1982, Genetics 102: 49-70; 2 = Sato, Russell, and Denell, 1983, Genetics 105: 357-70. | Enhances Pcl3. / Also deficient for Bc, Dox1, and fj (Deng and Rizki, 1988, Proc. Int. Congr. Genet., 16th, p. 192). ` Also deficient for fj and wt (Deng and Rizki, 1988). # Df(2R)PF1 cytology: Df(2R)57C5;57D1. origin: DEB induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Deficient for Pu. # Df(2R)pk: Deficiency (2R) prickle origin: X ray induced. discoverer: Gubb. deficiency cytology ref ( genetics _________________________________________________ Df(2R)pk78b pwn--sple- Df(2R)pk78d pwn--sple- Df(2R)pk78k 42E3;43C3 1, 2 pk--so- cn+ Df(2R)pk78n 2 pwn--sple- Df(2R)pk78r 43A1;43C7 2 pwn--sple- Df(2R)pk78s 42C1-7; 1, 2 pk--cn- 43F5-8 + In(2R)42C1-7; 59F5-8 Df(2R)pk78w pwn--sple- ( 1 = Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91; 2 = Gubb and Garcia-Bellido, 1982, J. Embryol. Exp. Morphol. 68: 37-57. # Df(2R)PK1 cytology: Df(2R)57C5;57F6. origin: DEB induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Deficient for Pu-Egfr. # Df(2R)PI12 cytology: Df(2R)57C4;57D8-9. origin: DEB induced. references: O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. McLean, Boswell, and O'Donnell, 1990, Genetics 126: 1007-19. genetics: Deficient for Pu-l(2)57Db. # Df(2R)Pl13 cytology: Df(2R)57B13-14;57D8-9 (O'Donnell). references: Schupbach, and Wieschaus, 1989, Genetics 121: 101-17. genetics: Uncovers tud. # Df(2R)PL3 cytology: Df(2R)57B18-20;57D8-9. origin: DEB induced. discoverer: O'Donnell. references: Schupbach and Wieschaus, 1986, Wilhelm Roux's Arch. Dev. Biol. 195: 302-17. O'Donnell, Boswell, Reynolds, and Mackay, 1989, Genetics 121: 273-80. genetics: Deficient for tud and Pu. # Df(2R)Pu-D17 cytology: Df(2R)57B4;58B. # Df(2R)PurF36: see Df(2R)F36 # Df(2R)Px: Deficiency (2R) Plexate deficiency cytology origin discov ( ref | comments ______________________________________________________________________ Df(2R)Px1 60B8-10; spont 1 1 Fo+ sp--ba- 60D1-2 Df(2R)Px2 60C5-6; X ray 3 1 sp+ ba--Pin- 60D9-10 Kr+ Df(2R)Px4 [see 4 2 Px--ba-; In(2LR)Px4] vesicles *Df(2R)Px5 spont in 4 4 sp+ bs--ba-; In(2LR)bwV1 vesicles; veins more regular than in Px1 *Df(2R)Px-Bsl / X ray 2 3 thick veins; blisters ( 1 = Bridges, 22f6; 2 = Oliver, 29b1; 3 = Schultz, 32l1; 4 = Thompson, 56f, 57. | 1 = Bridges, 1937, Cytologia, Fujii Jub. Vol. 2: 745-55; 2 = Burdick, 1956, DIS 30: 69; 3 = Oliver, 1939, DIS 11: 47; 4 = Thompson, 1963, DIS 38: 28. / Probably a Px deficiency (Bridges). Synonym: B5l. # Df(2R)R7 cytology: Complex. origin: / ray induced. references: Lasko and Pardue, 1988, Genetics 120: 495-502. genetics: Deficient for l(2)49Da - l(2)49Ea. # Df(2R)rl: Deficiency (2R) rolled deficiency cytology origin ( ref | genetics ___________________________________________________________ Df(2R)rl1 41A 2 2 rl- stw+ Df(2R)rl1G 41A 1 1, 2 l(2)41Ab--rl- Df(2R)rl2J 41A+ 1 1, 2 rl--uex- Df(2R)rl4J 41A 1 1, 2 l(2)41Ab--rl- Df(2R)rl5B 41A 1 1, 2 l(2)41Ab--rl- Df(2R)rl6C 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- Df(2R)rl9B 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- Df(2R)rl10a 41A ? 3 rl- stw+ Df(2R)rl10b / 41A ? rl--stw- Df(2R)rl10G 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- Df(2R)rl12E 41A 1 1, 2 l(2)41Ab--rl- Df(2R)rl13D 41A 1 1, 2 l(2)41Ab--rl- Df(2R)rl14C 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- Df(2R)rl18C 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- Df(2R)rl-B 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- Df(2R)rl-D 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- Df(2R)rl-F 41A 1 1, 2 l(2)41Ab--rl- Df(2R)rl-I 41A+ 1 1, 2 l(2)41Ab-- l(2)41Ae- ( 1 = Recovered as a detachment product of C(2L)RM, SH3/C(2R)RM, VK1, bw (Hilliker and Holm, 1975, Genetics 81: 705-21); 2 = Induced in a cn bw chromosome (Sharp et al., 1985). | 1 = Hilliker, 1976, Genetics 83: 765-82; 2 = Sharp, Hil- liker, and Holm, 1985, Genetics 110: 671-88; 3 = Tano, 1966, Jpn. J. Genet. 41: 299-308. / Stock listed (1982, DIS 57) but no references. # Df(2R)Rsp: Deficiency (3R) Responder cytology: Deficient for 2R heterochromatin. origin: X-ray-induced losses of sensitivity to distortion by SD. synonym: Df(2R)Rspins. references: Ganetzky, 1977, Genetics 86: 321-55. genetics: Insensitive to distortion by SD; lethal in combina- tion with Df(2R)M-S2-10; deficient for rl and lethals as tabu- lated below: deficiency deficient for ___________________________ Df(2R)Rsp1 Rsp--rl- Df(2R)Rsp11 Rsp--rl- Df(2R)Rsp31 Rsp--uex- # Df(2R)SB1 cytology: Df(2R)60F1;60F5. origin: X ray induced. references: Nusslein-Volhard, Wieschaus, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 267-82. Preiss, Rosenberg, Kienlin, Seifert, and Jackle, 1985, Nature 313: 27-32. Cote, Preiss, Haller, Schuh, Kienlin, Seifert, and Jackle, 1987, EMBO J. 6: 2793-2801. Baumgartner, Bopp, Burri, and Noll, 1987, Genes and Develop- ment 1: 1247-67. genetics: Deficient for gsb and Kr but not zip. Df(2R)gsb/Df(2R)SB1 embryos express gsb but not zip (Cote et al., 1987). molecular biology: Deletion for entire cloned Kr region; proxi- mal breakpoint at 0 to +3.5 kb on the molecular map (Cote et al., 1987). # Df(2L)sf-49 cytology: Df(2L)51B3-4;51C7-E2. # Df(2R)sple: Deficiency (2R) spiny legs cytology: Df(2R)42E3;43C3. origin: X ray induced. references: Gubb and Garcia-Bellido, 1982, J. Embryol. Exp. Morphol. 68: 37-57. genetics: Deficient for pk, pwn, and sple. # Df(2R)ST1 cytology: Df(2R)43B3-4;43E18. origin: / ray induced. discoverer: Tsubota. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. genetics: Deficient for pk, so, cos2 and cn, the heterozygotes showing small ocelli (Ashburner). # Df(2R)Sw: Deficiency (2R) Swedish cytology: Df(2R)60F3-4;60F5. origin: Natural condition of Swedish-b. discoverer: Catcheside, 36l20. genetics: No phenotypic effect. # Df(2R)TE19: see Df(2R)TE51D # Df(2R)TE51D origin: X ray induced in TE51D of Ising. discoverer: R. MacIntyre. synonym: Df(2R)TE19. genetics: w- rst-. deficiency cytology _________________________________ Df(2R)TE51D-11 51E3-4;52A6-10 Df(2R)TE51D-17 51D9-E1;51E5 Df(2R)TE51D-18 51E3;52C9-D1 Df(2R)TE51D-58 51D9-E1;52A13-B1 # Df(2R)trix: Deficiency (3R) transformer intersex cytology: Df(2R)51A2-4;51B6. discoverer: B.S. Baker. references: Breen and Duncan, 1986, Dev. Biol. 118: 442-56. Belote and Baker, 1987, Proc. Nat. Acad. Sci. USA 84: 8026- 30. genetics: Deficient for Asx and tra2. Homozygous trix larvae show abdominal setal-belt phenotype in thorax. # Df(2R)twi: Deficiency (2R) twist cytology: Df(2R)59C3-4;59D1-2 (Richards). origin: X ray induced. synonym: Df(1)twi-S60. references: Simpson, 1983, Genetics 105: 615-32. genetics: Deficient for twi. # Df(2R)V13: Deficiency (2R) Valencia cytology: Df(2R)49D-E;50B + T(2;3)60D;96F. origin: X ray induced with T(2;3)V13. references: Valencia, 1970, DIS 45: 37-38. # Df(2R)V30 cytology: Df(2R)41B;41C. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. # Df(2R)vg: Deficiency (2R) vestigial deficiency cytology origin ref ( genetics | ___________________________________________________________________________ Df(2R)vg33 49D;50A / ray 2 l(2)49Da- -l(2)49Fm-; vg/Df = vg Df(2R)vg52 49C-D;50B-C / ray Lasko vg/Df = vg Df(2R)vg56 49D;49F / ray 2, 5 vg--l(2)49Fa-; vg/Df = vg Df(2R)vg57 / ray Lasko vg/Df = vg Df(2R)vg62 49B8-D1;49E1-F2 / ray 2 l(2)49Da- -l(2)49Ea- Df(2R)vg79a 49D1;49E2 + neutrons 1, 2 In(2LR)34B2-C1; 49B12-C3 Df(2R)vg79b3 49C4;49E2 + / ray 1, 2 T(2;3)49C2-3;94A2-3 Df(2R)vg79d2 49C2-D2;49D7-E1 neutrons 1 vg- Df(2R)vg79d8 49C4-D1;49D7-E1 neutrons 1, 2 l(2)49Da- -l(2)49Ea- Df(2R)vg80l1 49D2-3;49E7-F1 neutrons 1 vg- Df(2R)vg81 / ray 2 l(2)49Da- -l(2)49Ea- Df(2R)vg83b 49B2-3;49E7-F1 / ray 1 vg- Df(2R)vg83c31 49C3-D2; / ray 1 vg- 49F15-50A1 Df(2R)vg83f15 49C3-D1;49E7-F1 / ray 1 l(2)49Da- -l(2)49Ea- Df(2R)vg83f36 49C3-D1;49E7-F1 / ray 1 vg- Df(2R)vg83f58 49B12-C1;49D7-E1 / ray 1 vg- Df(2R)vg83l2a 49D2-3;49D7-E1 neutrons 1 vg- Df(2R)vg83l-N 49C3-D1;50B9-C1 neutrons 1 vg- Df(2R)vg84f65 49B11-C1;49D7-F1 X ray 1 vg- Df(2R)vg84h49 49B2-5;49F10-11 X ray 1 vg- Df(2R)vg85f1 49B11-C1;49E7-F1 / ray 1 Df(2R)vg85f2 49B11-C1;49E7-F1 / ray 1 Df(2R)vg104 49C4;49F13 / ray 2 l(2)49Da- -l(2)Fk- Df(2R)vg106 / ray 2 l(2)49Da- -l(2)49Fj- Df(2R)vg107 / ray 2 l(2)49Da- -l(2)49Ea- Df(2R)vg120 / / ray 2 l(2)49Da- -l(2)49Ea- Df(2R)vg124 / / ray 2 l(2)49Da- -l(2)49Ea- Df(2R)vg133 / ray 2 l(2)49Da- -l(2)49Dc- Df(2R)vg135 48C-D;49D / ray 2 l(2)49Da- -l(2)49Dc- Df(2R)vg136 breakpoints not / ray 2, 5 vg- cytologically -l(2)49Ea- detectable Df(2R)vg-B ` 49D3-4; spont 2, 3, 5 l(2)49Da- 49F15-50A3 -l(2)49Fo- Df(2R)vg-C 49B2-3;49E7-F1 X ray 2, 3 sca--l(2)49Dc- Df(2R)vg-D ` - 49C1-2;49E4-5 spont 2, 3 sca--l(2)49Ea- *Df(2R)vg-l 49C2-D1;50A2-3 3 sca--l(2)49Dc- Df(2R)vg-P2 HD 2 l(2)49Da- -l(2)49Fm- Df(2R)vgR7 l(2)49Da- -l(2)49Ea- Df(2R)vg-S 49B12-C1; X ray 3, 4 sca--l(2)49Dc- 49F15-50A1 ( 1 = Alexandrov and Alexandrova, 1987, DIS 66: 185-87; 2 = Lasko and Pardue, 1988, Genetics 120: 495-502; 3 = Mor- gan, Bridges, and Schultz, 1938, Year Book-Carnegie Inst. Washington 37: 304-06; 4 = Muller, 1930, J. Genet. 22: 299-334. 5 = Williams and Bell, 1988, EMBO J. 7: 1355-63. | Homozygous lethal. / Heterozygous females have reduced fertility. ` Enhances BicD in heterozygotes (Mohler and Wieschaus, 1986, Genetics 112: 803-22). - Df(2R)vgD/+ flies show dominant flightlessness (Cripps, and Sparrow, 1989, Dev. Genet. 10: 98-105) and loss of bristles on legs and anterior dorsal thorax (Morgan, et al., 1938). # Df(2R)VV4L cytology: Df(2R)43B1;43B2. origin: X ray induced with Df(2R)VV4R. discoverer: Velissariou. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. # Df(2R)VV4R cytology: Df(2R)44F1;45A1-2. origin: X ray induced with Df(2R)VV4L. discoverer: Velissariou. references: Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. # Df(2R)WMG cytology: Df(2)52A4-B1;52D7-E1. discoverer: Gelbart. references: Chase and Kankel, 1987, J. Neurobiol. 18: 15-41. Davis and MacIntyre, 1988, Genetics 120: 755-66. # Df(2R)XTE-11 cytology: Df(2R)51E3-4;52A6-10. references: Chase and Kankel, 1987, J. Neurobiol. 18: 15-41. Davis and MacIntyre, 1988, Genetics 120: 755-66. genetics: Deficient for TE51D. # Df(2R)XTE-18 cytology: Df(2R)51E3-4;52C9-D1. references: Chase and Kankel, 1987, J. Neurobiol. 18: 15-41. Davis and MacIntyre, 1988, Genetics 120: 755-66. genetics: Deficient for TE51D. # Df(2R)Y: Deficiency (2R) Ytterborn cytology: Df(2R)59B;59F. origin: X ray induced. references: Ytterborn, 1968, Hereditas 59: 49-62.