# Df(3L)1-Df(3L)10 cytology: Df(3L)80F;80F. origin: Detachment of C(3L)RM/C(3R)RM. references: Marchant and Holm, 1988, Genetics 120: 519-32. deficiency genetics ___________________________________ Df(3L)1-16 l(3)80Fa- - l(3)80Fg- Df(3L)1-166 l(3)80Fg- - l(3)80Fj- Df(3L)2-66 l(3)80Fh- - l(3)80Fj- Df(3L)3-9 l(3)80Fj- Df(3L)5-84 l(3)80Fb- - l(3)80Fj- Df(3L)8A-80 l(3)80Ff- - l(3)80Fg- Df(3L)9-52 l(3)80Fa- - l(3)80Fj- Df(3L)9-56 l(3)80Fi- - l(3)80Fj- Df(3L)10-39 l(3)80Fd- - l(3)80Fj- Df(3L)10-58 l(3)80Fc- - l(3)80Fg- # Df(3L)29A6 cytology: Df(3L)66F3;67B1. origin: Induced by DEB (isolated as lethal over Df(3L)AC1). synonym: l(3)67Ee. references: Leicht and Bonner, 1988, Genetics 119: 579-93. genetics: No 67B heat shock puff. # Df(3L)1227 cytology: Df(3L)63C1-2;63F1-2. references: Fristrom. # Df(3L)AC1: Deficiency (3L) Adelaide Carpenter cytology: Df(3L)67A2;67D11-13. origin: Uncovered among progeny of males treated with ethyl methanesulfonate. discoverer: Carpenter. references: Leicht and Bonner, 1988, Genetics 119: 579-93. genetics: Deficient for M(3)67C [=M(3)i] (Leicht and Bonner, 1988) and (Tub67C (Matthews). # Df(3L)ASC: see Df(3L)Pc # Df(3L)BK origin: X ray induced in Dp(3;3)S2. references: Leicht and Bonner, 1988, DIS 67: 54-56. deficiency cytology new order ____________________________________________________________ Df(3L)BK9 68E2-3;69A1-2 61A - 68E2-3 | 69A1-2 - 100F Df(3L)BK10 71C1-2;71F4-5 61A - 71C1-2 | 71F4-5 - 100F Df(3L)BK15 68B1-2;68C6-8 61A - 68B1-2 | 68C6-8 - 100F Df(3L)BK140 ( 67F1;68C7-8 61A - 67F1 | 68C7-8 - 100F ( Also see Regan and Fuller, 1988, Genes Dev. 2: 82-92. # Df(3L)Brd: Deficiency (3L) Bearded origin: / ray induced. discoverer: Posakony. genetics: Deficient for Brd; phenotypically wild-type over Brd+. # In(3L)Brd: Inversion (3L) Bearded origin: / ray induced deriviatives of Brd1.. discoverer: Posakony. genetics: Mutant for Brd. inversion cytology synonym comments _________________________________________________________________ In(3L)Brd2 71A;71F In(3L)Brdm0 lethal; severe eye defect; > Brd1 In(3L)Brd3 70D-E;71A In(3L)Brdm1 lethal; severe eye defect; > Brd1 # Df(3L)brm11: Deficiency (3L) brahma cytology: Df(3L)71F;72D (Kennison). origin: Induced by P-M hybrid dysgenesis. discoverer: Kennison and Tamkun, 1987. genetics: brm-th-. Lethal in combination with Df(3L)st-g24 = Df(3L)72D1-2;73A9-10 but survives in combination with Df(3L)st-e4 = Df(3L)72D5-10;73A5 and Df(3L)st-b11 = Df(3L)72D7-9;73D1-2. # Df(3L)Cat: Deficiency (3L) Catalase cytology: Df(3L)75C1-2;75F1. origin: / ray induced. synonym: Df(3L)CatDH104. references: Mackay, Hollar, and Bewley, 1986, Genetics 113: s31. Bewley, Mackay, and Cook, 1986, Genetics 113: 919-38. genetics: Deficiency heterozygotes show dosage effect for catalase activity. #*Df(3L)D: see T(Y;2;3)D # Df(3L)DTS5-3 cytology: Df(3L)72F3-4;73E2-F1 (Ashburner). origin: X-ray-induced reversion of dominant effect of l(3)73Ai selected at 29. discoverer: Faithfull. synonym: Df(3L)DTS-5R+3. genetics: Deficient for l(3)73Ai. # Df(3L)DTS5-4 cytology: Df(3L)72D3-6;73B6-C4 + T(Y;3)CA16 (broken at 90B-C). origin: X-ray-induced revertant of dominant effect of l(3)DTS- 5. discoverer: Faithfull. synonym: Df(3L)DTS-5R+4; Df(3L)stA. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91 (listed here incorrectly as Df(3L)DTS-5R+3). genetics: Deficient for l(3)73Ai, st and tra but not for as or th. # Df(3L)E origin: X ray induced. genetics: Homozygous lethal. deficiency cytology ref ( comments mol biol | _________________________________________________________________ Df(3L)E5 ?;73A9-10 1 tra+ +80 kb (prox.) Df(3L)E34 / 73A1-2;? 1, 2 tra- -36 kb (dist.) Df(3L)E36 ` ?;73B1-2 1, 2 tra- +120 kb (prox.) Df(3L)E48 ?;73A11 1 tra- +90 kb (prox.) Df(3L)E52 73A1-2;73A9-10 1 tra- -38 kb (dist.); +85 kb (prox.) ( 1 = Butler, Pirrotta, Irminger-Finger, and Nothiger, 1986, EMBO J. 5: 3607-13; 2 = Henkemeyer, Gertler, Goodman, and Hoffmann, 1987, Cell 51: 821-28. | The zero coordinate used in locating the molecular lesions is the 73A3-4 breakpoint of In(3LR)sta27, "+" values to the right, "-" values to the left (McKeown, Belote, and Baker, 1987, Cell 48: 489-99). The distal and proximal molecular breaks of the deficiencies made by Butler et al, 1986, were estimated using this zero coordinate. (BamHI site, midway between Df(3L)E5 and Df(3L)E52, was the original zero coor- dinate of Butler et al.). / Synonym: Df(3L)st-E34; includes st-l(3)73Bb but not l(3)73Bc (Henkemeyer et al., 1987). ` Synonym: Df(3L)st-E36; includes st-Abl but not l(3)73Bb (Henkemeyer et al., 1987). # Df(3L)e146c4 cytology: Df(3L)67A;67A. genetics: l(3)67Ac-l(3)67Ad. # Df(3L)emc: Deficiency (3L) extra macrochaetae cytology: Df(3L)61C5-6;61D3-4. origin: X ray induced. discoverer: Ellis. genetics: Deficient for emc; rare homozygous escapers. # Df(3L)emc-E12 cytology: Df(3L)61A;61D3. references: Alonso, and Garcia-Bellido 1988, Roux's Arch. Dev. Biol. 197: 328-38. genetics: Deficient for emc. # Df(3L)Est6: Deficiency (3L) Esterase 6 discoverer: Richmond. # Df(3L)Ez: Deficiency 3L Enhancer of zeste references: Jones and Gelbart, 1990, in press. genetics: Deficient for E(z). deficiency cytology origin synonym ___________________________________________________________ Df(3L)Ez1 67E3-4;67F1-3 / ray of E(z)1 E(z)1R2 Df(3L)Ez2 67E1-2;67E5-7 / ray of E(z)1 E(z)1R3 + In(3L)64B;67E Df(3L)Ez3 67E3-4;67E6-7 / ray of E(z)1 E(z)1R9 Df(3L)Ez4 67E1-4;68A1-2 / ray of E(z)1 E(z)1R12 Df(3L)Ez5 67D9-13;68F / ray of E(z)1 E(z)1R13 Df(3L)Ez6 67E1-2;67E3-5 / ray of E(z)60 E(z)S1R1 Df(3L)Ez7 67E1-4;67F1-3 EMS E(z)S6 # Df(3L)fz-CAL5: Deficiency (3L) frizzled cytology: Df(3L)70C2-7;70E1-3. origin: Hybrid dysgenesis induced. references: Adler, Charlton, and Vinson, 1987, Dev. Genet. 8: 99-119. genetics: Strong fz phenotype over fz; lethal over fzD21, fzM21. # Df(3L)fz-D21 cytology: Df(3L)70D3;70E3-8. origin: / ray induced. discoverer: Adler. references: Freeman, Nusslein-Volhard, and Glover, 1986, Cell 46: 457-58. Adler, Charlton, and Vinson, 1987, Dev. Genet. 8: 99-119. genetics: Deficient for fz and gnu (Freeman et al., 1986). # Df(3L)fz-GF3b cytology: Df(3L)70B;70C6. # Df(3L)fz-GS1a cytology: Df(3L)70C6-15;70E4-6. # Df(3L)fz-M21 cytology: Df(3L)70D2-3;71E4-5. origin: / ray induced. discoverer: Adler. references: Freeman, Nusslein-Volhard, and Glover, 1986, Cell 46: 457-58. Adler, Charlton, and Vinson, 1987, Dev. Genet. 8: 99-119. genetics: Deficient for fz. #*Df(3L)Gl1: Deficiency (3L) Glued cytology: Df(3L)70C;71B. origin: X ray induced. synonym: Df(2L)Glrv1; Df(3L)Gl+R1. references: Harte and Kankel, 1982, Genetics 101: 477-501. genetics: Deficient for Gl and fz. Lethal over In(3L)D, D3. # Df(3L)Gl2 cytology: Df(3L)70C;70F. origin: X ray induced. synonym: Df(3L)Glrv21; Df(3L)Gl+R2. references: Harte and Kankel, 1982, Genetics 101: 477-501. Garen, Miller, and Paco-Larson, 1984, Genetics 107: 645-55. genetics: Deficient for the entire Gl region and fz. Lethal over In(3L)D, D3. # In(3L)h: Inversion (3L) hairy inversion cytology origin ref ( genetics ________________________________________________________________________ *In(3L)h10 61A2-3;66D X ray 5 mutant for h *In(3L)h11 66D11-12;80C X ray 5 mutant for h *In(3L)h16 66D14-E1;80F X ray 2, 3, 4 homoz. semilethal; h16/h variegated In(3L)h40 66D10-15;72C hybrid 2 homoz. lethal dysgenesis In(3L)h42 | 65B1-2;66D6-10 X ray 1, 2 homoz. lethal In(3L)h44 66D5-11;80C X ray 1 mutant for h ( 1 = Howard, Ingham, and Rushlow, 1988, Genes Dev. 2: 1037-46; 2 = Ingham, Pinchin, Howard, and Ish-Horowicz, 1985, Genetics 111: 463-86; 3 = Jeffery, 1971, DIS 47: 37; 4 = Jeffery, 1979, Genetics 91: 105-25; 5 = Ward and Alexander, 1957, Genetics 42: 42-54. See references for synonyms. | Molecular biology: 66D break of In(3L)h42 and In(3L)h44 located at -5.15 to -2.5 kb and -9.35 to -6.8 kb, respectively, on the DNA map of h (Howard et al., 1988); "+" values to the right, "-" values to the left. The coordinate system places 0 at the start of transcription (Rushlow). #*Df(3L)h100.390: Deficiency (3L) hairy cytology: Df(3L)66D2-5;66D14-E1. origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42-54. genetics: Deficient for h. # Df(3L)h-i22 cytology: Df(3L)66D10-11;66E1-2. origin: X ray induced. discoverer: Belote. references: Ingham, Pinchin, Howard, and Ish-Horowicz, 1985, Genetics 111: 463-86. genetics: Deficient for h and the chorion protein genes on 3L (Cp-15, Cp-16, Cp-17, and Cp-18), and abd but not se. Homozy- gous lethal. # Df(3L)Hn: Deficiency (3L) Henna cytology: Df(3L)66A;66B. origin: X ray induced simultaneously with T(2;3)Hn = T(2;3)53E-54A;77A;94F;96A. discoverer: Van Atta, 30k. references: 1932, Am. Nat. 66: 93-95. 1932, Genetics 17: 637-59. Lewis, 1956, DIS 30: 130. genetics: Mutant or deficient for Hn. Homozygous lethal. # Df(3L)in61: Deficiency (3L) inturned cytology: Df(3L)76F;77D. references: Arajarvi and Hannah-Alava, 1969, DIS 44: 73-74. genetics: Deficient for in. # Df(3L)JK18: see Df(3L)kto2 #*Df(3L)K: Deficiency (3L) of Krivshenko cytology: Df(3L)61A;61C1-2; an apparent terminal deficiency. origin: Probably X ray induced. discoverer: Krivshenko, 56l4. synonym: Df-3LK. references: 1959, DIS 33: 95. # Df(3L)kto2: Deficiency (3L) kohtalo cytology: Df(3L)76B1-2;76D5 (Ashburner). origin: Induced by P-M hybrid dysgenesis. discoverer: Kennison, 1987. synonym: Df(3L)JK18. genetics: Deficient for kto and ash1. # Df(3L)l3 cytology: Df(3L)68A8-B1;68B4-C1. Status of 68A7 not clear. origin: Induced by ethyl methanesulfonate. references: Campbell, Hilliker, and Philips, 1986, Genetics 112: 205-15. genetics: Includes l(3)68Ba-l(3)68Be. Not deficient for Sod. # Df(3L)lxd: Deficiency (3L) low xanthine dehydrogenase references: Schott and Finnerty, 1983, Genetics 104: s62-63. Schott, Baldwin, and Finnerty, 1986, Biochem. Genet. 24: 509-27. deficiency cytology genetics ___________________________________________ Df(3L)lxd2 68A2-3;68C5-7 lxd- Df(3L)lxd6 ( 67E1-2;68C1-2 hay-- lxd- Df(3L)lxd8 68A2-3;68A5-6 lxd- Df(3L)lxd9 | 68A3-4;68B4-C1 lxd-- sod- Df(3L)lxd15 67E;68C10-15 hay-- lxd- ( See Regan and Fuller, 1988, Genes Dev. 2: 82-92. | See Campbell, Hilliker, and Phillips, 1986, Genetics 112: 205-15. # Df(3L)Ly: Deficiency (3L) Lyra cytology: Df(3L)70A2-3;70A5-6. origin: X ray induced. discoverer: Dubinin, 1929. references: Morgan, Bridges, and Schultz, 1937, Year Book - Carnegie Inst. Washington 36: 301. genetics: Associated with the mutant, Ly. Lethal in combina- tion with Df(3L)M69E. # Df(3L)Ly2 cytology: Df(3L)70A2-3;70A5-6. Same as Df(3L)Ly (Zhimulev and Feldman, 1982). origin: Spontaneous (possibly caused by male recombination inducer). references: Waddle, 1977, DIS 52: 3. Zhimulev and Feldman, 1982, DIS 58: 152. genetics: Deficient for Ly. Phenotype of Ly2 similar to Ly except that eyes tend to be rougher. #*Df(3L)M69E cytology: Probably includes bands in 70A. origin: X ray induced. discoverer: Demerec, 33j25. synonym: *Df(3L)M-h33j. references: 1935, DIS 3: 27. Coyne, 1935, DIS 4: 59. Mossige, 1938, Hereditas 24: 110-16. genetics: Deficient for M(3)69E; lethal homozygous and in com- bination with Df(3L)Ly. # *Df(3L)M-h33j: see Df(3L)M69E # Df(3L)Mg26: Deficiency (3L) Mglinetz cytology: Df(3L)66C;66D. origin: / ray induced. references: Mglinetz, 1972, Genetika (Moscow) 8: 82-92. # Df(3L)Mg27 cytology: Df(3L)61C;66D. origin: / ray induced. references: Mglinetz, 1972, Genetika (Moscow) 8: 82-92. #*Df(3L)Mz: Deficiency (3L) from Minute (2) z stock cytology: Loss of several bands from tip of 3L(61A). origin: Spontaneous. discoverer: Bridges, 36h28. references: CP627. # Df(3L)N264-6: see T(1;3)N264-6 # Df(3L)P20: Deficiency (3L) Pasadena 20 cytology: Df(3L)67F;68E3-4. origin: Recombinant from Tp(3;3)P20/+. references: Lewis, 1980, DIS 55: 207-08. genetics: Df(3L)P20/+ flies slightly Minute and seem to have reduced fertility in females. # Df(3L)Pc: Deficiency (3L) Polycomb deficiency cytology discoverer ref ( genetics _______________________________________________________________ Df(3L)Pc | 78D1-2;79A4-C1 Jurgens 1 Pc- Df(3L)Pc-MK 78A3;79E1-2 Denell 3-5 Pc- *Df(3L)Pc-T6 / 77E1;79A1 Tiong ri-Pc-M Df(3L)Pc-T7 / 78E2-3;79E5 Tiong 2 ri+Pc- *Df(3L)Pc-W2 Williams Pc- ( 1 = Haynie, 1983, Dev. Biol. 100: 399-411; 2 = Kennison and Russell, 1987, Genetics 116: 75-86; 3 = Sato and Denell, 1985, Dev. Biol. 110: 53-64; 4 = Sato, Hayes, and Denell, 1984, Dev. Genet. 4: 185-98; 5 = Sato, Russell, and Denell, 1983, Genetics 105: 357-70. | Synonym: Df(3L)ASC. / Origin: / ray induced. # Df(3L)Pst8: see Df(3L)st8P # Df(3L)Pst-B7: see Df(3L)st7P # Df(3L)R: Deficiency (3L) Rough discoverer: J. Bonner. references: Johnson and Friedman, 1983, Proc. Nat. Acad. Sci. USA 80: 2990-94. Sliter, Henrich, Tucker, and Gilbert, 1989, Genetics 123: 327-36. deficiency origin cytology genetics ______________________________________________________________ Df(3L)R 62B7;62B12 Aprt- R- Df(3L)R-E X ray 62B8-9;62B12-C1 R- - l(3)62Bi- Df(3L)R-G2 / ray 62B2-4;62B11-12 l(3)62Ba- - l(2)62Bg- Df(3L)R-G5 / ray 62A10-B1;62C4-D1 l(3)62Ba- - l(2)62Ca- Df(3L)R-G7 / ray 62B8-9;62F2-5 R- - ecd- Df(3L)R-R2 X ray 62B2-4;62D3-5 l(3)62Ba- - ecd- # Df(3L)ri79c: Deficiency (3L) radius incompletus cytology: Df(3L)77B-C;77F-78A. discoverer: Jurgens. references: Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95. genetics: Deficient for kni and ri. # Df(3L)ri-K2 cytology: Df(3L)76D;77E-F. discoverer: Gubb. references: Garcia-Bellido, Moscoso del Prado, and Botas, 1983, Mol. Gen. Genet. 192: 253-63. genetics: Deficient for ri. #*Df(3L)ru100.392: Deficiency (3L) roughoid cytology: Df(3L)61E;62A10-B1. origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42- 54. genetics: Deficient for ru. #*Df(3L)ru100.393 cytology: Df(3L)61E;62A4-6. origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42-54. genetics: Deficient for ru. #*Df(3L)ru300.234 cytology: Df(3L)61E;62A2-4. origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42-54. genetics: Deficient for ru. #*Df(3L)ru-K1: Deficiency (3L) roughoid of Krivshenko cytology: Df(3L)62A12-B1;62B2-3. origin: X ray induced. discoverer: Krivshenko, 1957. references: 1958, DIS 32: 81. genetics: Has rough and slightly reduced eyes in combination with ru but, judging from cytology, probably not deficient for ru. #*Df(3L)ru-K2 cytology: Df(3L)61F4-5;62A10-B1. origin: X ray induced. discoverer: Krivshenko, 1957. references: 1958, DIS 32: 81. genetics: Deficient for ru. # Df(3L)st: Deficiency (3L) scarlet molecular deficiency cytology origin discoverer synonym ref ( genetics biology | ____________________________________________________________________________________________________________________________________________ Df(3L)st 72D7;74A3 3, 10 st- tra- Df(3L)st2 / 73A2-3;73A5 / ray Faithfull 1, 9 st- Df(3L)st3 72E5-F1;73A3-4 / ray Faithfull 1, 9 th st- Df(3L)st4 72D7-11;73B7-C11 / ray Faithfull 1, 6, 9 st- tra- Df(3L)st6 72E1-2;73A3-4 / ray Faithfull 9 st- tra+ Df(3L)st7 73A3-4;74A3 / ray Faithfull 9 st- tra- Df(3L)st7P 73A1-2;73A7-9 X ray Bonner PstB7 8 l(3)73Aa--l(3)73Ag- tra+ +80 to +85 + In(3L)P Df(3L)st8P 72E4;73B4 X ray Bonner Pst8 l(3)73Aa--Abl- db+ + In(3L)P Df(3L)st62 73A2-3;73B3-5 X ray 100.62 6,8,12 l(3)73Aa--Abl- db+ Df(3L)st100.62 72F3-7;73B3 13 st- Df(3L)st103 73E3;74A6 X ray S. Smith SS103 2, 3 bul--tra- Df(3L)st106 72E3;73A3-4 X ray S. Smith SS106 2, 11, 12 bul--tra- *Df(3L)st171 72E4-5;74C2-3 X ray 100.171 13 st- *Df(3L)st200 72E4-5;73A10-B1 X ray 100.200 13 st- Df(3L)st-a20 73A3;73A4 X ray Belote 4, 8 l(3)73Aa+ l(3)73Ab--st- -45 to -40; l(3)73Ac+ +45 to +55 Df(3L)st-b8 72D5-11;74B2 st- Df(3L)st-b11 72D10-11;73D1-2 X ray Belote 4 l(3)73Aa--db- Df(3L)st-e4 72D5-10;73A5 X ray Belote 4, 8 l(3)73Aa--st- l(3)73Ac+ +60 *Df(3L)st-e5 72E2;73D4 + X ray Belote 4 l(3)73Aa--Abl- In(3L)72E5-F1;73A1-2 Df(3L)st-E5 ?;73A9-10 b st-tra+ +2 to 0 Df(3L)st-e10 {73A;73A} dysgenesis Green, 81e10 81e st- lethal Df(3L)st-E34 73A1-2; ? b st-tra+ +2 to 0 Df(3L)st-E36 ?; 73B1-2 b st-tra- ~ +115 Df(3L)st-E48 ?; 73A11 b st-tra- ~ -33 Df(3L)st-E52 73A1-2; 73A 9-10 b st-tra- -6 to -13 b st-tra- ~ +117; -2 to -6 Df(3L)st-f13 72C1-D1;73A3-4 X ray Belote 4, 8 l(3)73Aa--st- l(3)73Ac+ +20 to +25 Df(3L)st-g18 72E2-7;74F4-75A2 + X ray Belote 4, 5 l(3)73Aa--db- ` In(3LR)65A1-2;99A1-2 Df(3L)st-g24 72D1-2;73A9-10 X ray Belote 4, 6, 8 l(3)73Aa--tra- l(3)73Aj+ +105 *Df(3L)st-g82 72D10-11;73B1-2 X ray Belote 4 l(3)73Aa--tra- l(3)73Aj+ (see Tp(3;1)st-g82) Df(3L)st-j7 73A1-2;73B1-2 X ray Belote 4, 6, 8 l(3)73Aa--l(3)73Aj- +140 Df(3L)st-j7;RB87 73A1-2;73B1-2;87D dysgenesis 8 Df(3L)st-j11 72E2;73E1-2 X ray Belote 4 st- Df(3L)st-k2 73A2-3;73D2-3 dysgenesis Green, 81k7 81K7(2) Df(3L)st-k3 {73A;73A} dysgenesis Green, 81k19 81K19(3) st- lethal Df(3L)st-k7 72A2-73A4;74E1-2 dysgenesis Green, 81k19 81K19(7) st- Df(3L)st-k10 73A3-4;73D1-2 dysgenesis Green, 81k17 81K17(12) 5 st- lethal Df(3L)st-LM3 {73A;73A} X ray Marsh and Mock 7 bul- st--l(3)73Ai- Df(3L)st-LM19 {73A;73A} X ray Marsh and Mock 7 bul- st--l(3)73Ai- ( 1 = Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91; 2 = Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95; 3 = Baker and Ridge, 1980, Genetics 94: 383-423; 4 = Belote and McKeown; 5 = Belote and McKeown, 1985, DIS 61: 33-34; 6 = Butler, Pirotta, Irminger-Finger, and Nothiger, 1986, EMBO J. 5: 3607-13; 7 = Henkemeyer, Gertler, Goodman, and Hoffmann, 1987, Cell 51: 821-28; 8 = Marsh and Mock, 1985, DIS 61: 214; 9 = McKeown, Belote, and Baker, 1987, Cell 48: 489-99; 10 = Velissariou and Ashburner, 1981, Chromo- soma 84: 173-85; 11 = Voelker, Ohnishi, and Langley, 1978, Biochem. Genet. 17: 947-56; 12 = Walker and Ashburner, 1981, Cell 26: 269-77; 13 = Ward and Alexander, 1957, Genetics 42: 42-54. | DNA coordinates (kb) of proximal breakpoints in the walk in region 73A-B of McKeown and Belote, which originates at the left breakpoint of In(3LR)sta27 ("+" values to right, "-" values to left). Df(3L)st-E coordinates from Butler et al., 1986; coordinate 0 halfway between right breakpoints of Df(3L)st-E5 and Df(3L)st-E52; positive values to the left. / Semilethal in combination with TM3; lethal in combination with TM1 and TM6 (Ashburner). ` Heterozygote viable but weak. # Df(3L)std11: see In(3L)std11 # Df(3L)th: Deficiency (3L) thread deficiency cytology origin ( ref | genetics _____________________________________________________________ Df(3L)th1 / 71F3-5;72D6-8 1 1, 4 th- Df(3L)th2 / 70F1-3;72E3-5 1 1, 4 th- Df(3L)th45 72A5;72D6 2 2 th- Df(3L)th70i 72A2;72D6 2 3 th- Df(3L)th70kI 71C3-4;72C1-2 2 3 th- Df(3L)th70kII 71F3-4;73A3-4 2 3 th- Df(3L)th70l 72A2;72D 2 3 th- Df(3L)th102 72B1;72D12 2 2, 5 th--Pgm- *Df(3L)th105 72A2-B1;73A4-5 2 6 th--st- Df(3L)th112 71F3-5;72D12 2 2 th- Df(3L)th113 72A2;72D1-2 2 2 th- Df(3L)th117 72A1;72D5 2 2, 5 th--Pgm- ( 1 = / ray induced; 2 = X ray induced. | 1 = Ashburner, Angel, Detwiler, Faithfull, Gubb, Harrington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91; 2 = Ashburner, Faithfull, Littlewood, Richards, Smith, Velissariou, and Woodruff, 1980, DIS 55: 193-95. 3 = Korge, 1972, DIS 48: 20; 4 = Velissariou and Ashburner, 1981, Chromosoma 84: 173-85; 5 = Voelker, Ohnishi, and Langley, 1978, Biochem. Genet. 17: 769-83; 6 = Ward and Alexander, 1957, Genetics 42: 42-54. / Dominant female-sterile. # Df(3L)tra: Deficiency (3L) transformer cytology: Df(3L)73A4;74A1-2. origin: X ray induced. discoverer: B.S. Baker. references: McKeown, Belote, and Baker, 1987, Cell 48: 489-99. genetics: Deficient for l(3)73Ac through db; also includes C- abl; does not include st; broken between st+ and the next lethal complementation group to the right. molecular biology: Distal breakpoint in the vicinity of +25 to +30 kb, "+" values to the right, "-" value to the left (McKeown et al., 1987). # Df(3L)V13: see Tp(3;3)V13 # Df(3L)V127 cytology: Df(3L)71C1;71C2. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. # Df(3L)ve: Deficiency (3L) veinlet cytology: Df(3L)61E1;62A2-3. 61E and 61F not puffed. origin: X ray induced. references: Korge, 1970, Chromosoma 30: 430-64. genetics: Deficient for ve. # Df(3L)vin: Deficiency (3L) vin deficiency cytology origin ( ref | genetics _____________________________________________________________________ Df(3L)vin1 67E5-7;68E3-4 1 1, 2 rs-- vin- Df(3L)vin2 67F2-3;68D6 2 1 rs-- vin- Df(3L)vin3 68C5-6;68E3-4 1 1, 2, 3, 4 rt-- Lsp2- Df(3L)vin4 68B1-3;68F3-6 1 1, 2, 3, 6 rt-- Lsp2- Df(3L)vin5 68A2-3;69A1-3 1 1, 2, 4 Sgs3-- Lsp2- Df(3L)vin6 68C8-11;69A4-5 1 1, 2 vin-- app- Df(3L)vin7 68C8-11;69B4-5 1 1, 2 rt-- app- Df(3L)vin8 / 68C2-3;68F3-6 5 vin- Df(3L)vin9 / 68C5-6;69A5-B1 5 vin- Df(3L)vin10 ` vin- Df(3L)vin11 ` vin- Df(3L)vin66 68A2-3;68D3 1 1, 2 Sgs3-- vin- ( 1 = / ray induced; 2 = X ray induced. | 1 = Akam, Roberts, Richards, and Ashburner, 1978, Cell 13: 215-25; 2 = Crosby and Meyerowitz, 1986, Genetics 112: 785-802; 3 = Garcia-Bellido, Moscoso del Prado, and Botas, 1983, Mol. Gen. Genet. 192: 253-63; 4 = Gautam, 1983, Mol. Gen. Genet. 189: 495-500; 5 = D.B. Roberts; 6 = Schott, Baldwin, and Finnerty, 1986, Biochem. Genet. 24: 509-27. / Discoverer: Hoogwerf. ` No cytology or genetics given (Ashburner). #*Df(3L)Vn: Deficiency (3L) Vein cytology: Df(3L)64C12-D1;65D2-E1. origin: Spontaneous. discoverer: Mohr, 28j21. references: 1932, Proc. Intern. Congr. Genet., 6th., Vol 1: 199-212. 1938, Norske Videnskaps-Akad. 4: 1-7. Mohr and Mossige, 1943, Norske Videnskaps-Akad. 7: 1-51 (fig.). genetics: Deficient for jv, dv, and Me but not for abd, Hn, or se. Mutant or deficient for Vn. #*Df(3L)VV8 cytology: Df(3L)74B1-2;74F1-2. origin: / ray induced. discoverer: Velissariou. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. # Df(3L)VW1 cytology: Df(3L)69E2-F1;70C1. origin: / ray induced. discoverer: Walker. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. genetics: Minute phenotype; presumably deficient for M(3)69E. # Df(3L)VW3 cytology: Df(3L)76A3;76B2. origin: / ray induced. discoverer: Walker. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. genetics: Minute phenotype; presumably deficient for M(3)76A. # Df(3L)W: Deficiency (3L) Wrinkled origin: X ray induced. synonym: Df(3L)Wrv; Df(3L)W+R. genetics: Deficient for W. deficiency cytology discoverer ref ( __________________________________________________ Df(3L)W4 | 75B8-11;75C5-7 Segraves 2, 3 *Df(3L)W7 74D3-5;75C3-7 Faithfull 1 Df(3L)W10 / 75A6-7;75C1-2 Segraves 2, 3 ( 1 = Ashburner, Faithfull, Littlewood, Richards, Smith, Vel- issariou and Woodruff, 1980, DIS 55: 193-95; 2 = Segraves and Hogness, 1984, Genetics 107: s96-97. 3 = Seagraves and Hogness, 1990, Genes Dev. 4: 204-19. | Proximal to 75B puff. / Includes 75B puff and E75 gene (Segraves and Hogness, 1984). # Df(3L)X37 genetics: Deficient for Src1. # Df(3R)+1 cytology: Df(3R)92A11-B2;92C3-D1. genetics: Deficient for l(3)SG65. # Df(3R)1c77: see Df(3R)Tpl2 # Df(3R)3g74: see Df(3R)Tpl1 # Df(3R)4-7 cytology: Df(3R)81F;81F. genetics: Deficient for l(3)81Fa-l(3)81Fb. # Df(3R)4SCB cytology: Df(3R)84A6-B1;84B2-3. discoverer: G. Jurgens. references: Struhl, 1981, Nature 292: 635-38. Garber, Kuroiwa, and Gehring, 1983, EMBO J. 2: 2027-36. Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95. genetics: Deficient for Scr, ftz, and Antp. Homozygous lethal (Howard and Ingham, 1986, Cell 44: 949-57). molecular biology: Deletes sequences to left of a point 100 kb to the left of the proximal breakpoint of In(3R)Hu (Garber et al., 1984). # Df(3R)5B-RXP cytology: Df(3R)97A;98A1-2. discoverer: Anderson. # Df(3R)5f77: see Df(3R)Tpl3 # Df(3R)9A99 cytology: Df(3R)83F2-84A1;84B1-2. Defines maximum leftward extent of Antp. discoverer: G. Jurgens. references: Garber, Kuroiwa, and Gehring, 1983, EMBO J. 2: 2027-36. Kuroiwa, Hafen, and Gehring, 1984, Cell 37: 825-31. Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95. genetics: Deficient for Scr and ftz. Complements all Antp alleles tested. molecular biology: Proximal breakpoint between coordinates +170 and +180 on DNA map of region 84B1-2 (Garber et al., 1983). # Df(3R)10-65 cytology: Df(3R)81F;81F. genetics: Deficient for l(3)81Fa-l(3)81Fb. # Df(3R)10d77-7: see Df(3R)Tpl4 # Df(3R)25g77: see Df(3R)Tpl5 # Df(3R)26b77: see Df(3R)Tpl6 # Df(3R)28b77: see Df(3R)Tpl7 # Df(3R)28f77: see Df(3R)Tpl8 # Df(3R)29c76: see Df(3R)Tpl9 # Df(3R)30c76: see Df(3R)Tpl10 #*Df(3R)89EF cytology: Df(3R)89D7-E1;90A2-3. origin: Synthetic. Made by combining the 4P3RD element of one T(3;4) with the 3RP4D element of another. discoverer: Dubovsky and Kelstein. references: 1936, Eksperim. Med. No. 11: 65-84. Kelstein, 1938, Biol. Zh. (Moscow) 7: 1145-69. Pipkin, 1959, Texas Univ. Publ. 5914: 69-88. genetics: One of a series of deficiencies for the middle of 3R synthesized and carefully studied by Dubovsky and Kelstein. Deficient for abdominal components of BXC. Heterozygous male has rotated genitalia which may be feminized both in structure and color, has sex combs. Heterozygous female sterile. # Df(3R)109 references: Casanova, Sanchez-Herrero, and Morata, 1986, Cell 47: 627-36. genetics: Deficient for Ubx and iab2 but not iab5-7. # Df(3R)148.5: see Df(3R)Cha-M1 # Df(3R)159.22 cytology: Df(3R)87E3-4;87E6-8. origin: Induced by diepoxybutane. references: Nagoshi and Gelbart, 1987, Genetics 117: 487-502. genetics: Deficient for l(3)87Ee-l(3)87Ef. molecular biology: Distal breakpoint 3-8 kb proximal to the distal breakpoint of Df(3R)Ace-HD1 at 72.5 - 77.8 kb (DNA walk of Bender, Spierer and Hogness, 1983, J. Mol. Biol. 168: 17- 33). # Df(3R)229: see Df(3R)E-229 # Df(3R)293 cytology: Df(3R)87E;88A. references: Parkhurst, Harrison, Remington, Spana, Kelley, Coyne, and Corcas, 1988, Genes Dev. 2: 1205-15. # Df(3R)A41 cytology: Df(3R)84B1-2;84D1-2. origin: X ray induced. discoverer: Abbott, 1985. references: Cavener, Otteson, and Kaufman, 1986, Genetics 114: 111-23. Cavener, Corbett, Cox, and Whetten, 1986, EMBO J. 5: 2939-48. Whetten, Organ, Krasney, Cox-Foster, and Cavener, 1988, Genet- ics 120: 475-84. genetics: Deficient for Antp but not for ftz. molecular biology: Left breakpoint at about +140 kb on the molecular map of Cavener et al., (1986). # Df(3R)A113 cytology: Df(3R)100A-B;100F. references: Van Vactor, Krantz, Reinke, and Zipursky, 1988, Cell 52: 281-90. # Df(3R)Ace-HD1: Deficiency (3R) Acetylcholinesterase cytology: Df(3R)87E3-4;87E5-6. origin: Hybrid dysgenesis. references: Nagoshi and Gelbart, 1987, Genetics 117: 487-502. genetics: Deficient for Ace-l(3)87Ee; does not fully remove Ace activity, but behaves as recessive Ace lethal. molecular biology: Proximal breakpoint between +49 and +50.5 kb; distal breakpoint between +72.5 and +77.8 kb (DNA walk of Bender, Spierer, and Hogness, 1983, J. Mol. Biol. 168: 17- 33). # Df(3R)Aldoxn1: Deficiency (1) Aldehyde oxidase cytology: Df(3R)89A1-2. origin: Spontaneous. references: Langhout and van Breugel, 1985, DIS 61: 181. genetics: Deficient for Aldox. # Df(3R)Antp73b+RX1: see Df(3R)Antp-X1 # Df(3R)Antp73b+RX2: see Df(3R)Antp-X2 # Df(3R)Antp73b+RX3: see Df(3R)Antp-X1 # Df(3R)Antp73b+RX4: see Df(3R)Antp-X2 # Df(3R)Antp+R1P: see Df(3R)Antp1P # Df(3R)AntpNs+R17: see Df(3R)Antp17 # Df(3R)AntpNs+RC7: see Df(3R)Antp7 # Df(3R)AntpBLdsxDrv3R: see In(3R)AntpBLdsxDrv3R # Df(3R)AntprA60: see Df(3R)Antp2 # Df(3R)AntprA75: see Df(3R)Antp6 # Df(3R)Antp1P: Deficiency (3R) Antennapedia cytology: Df(3R)84B3;84D1-2 + In(3R)84B3;85C2-3. origin: Deficient recombinant between In(3R)Antprv1P (also a transposition) and a normal sequence. discoverer: Green. synonym: Df(3R)Antp+R1P. references: Lewis, Kaufman, and Denell, 1980, DIS 55: 85-87. Lewis, Kaufman, Denell, and Tallerico, 1980, Genetics 95: 367-81. genetics: Deficient for the distal portion of the 84B1-2 doub- let and reverted for Antp; deficient for roe (Lewis et al., 1980). # Df(3R)Antp2 cytology: Df(3R)84B2;84D3. synonym: Df(3R)AntprA60. origin: X ray induced. references: Abbott and Kaufman, 1986, Genetics 114: 919-42. genetics: Not Antp over wild-type. Complements Antp23 and Antp1. # Df(3R)Ant6 cytology: Df(3R)84B2;84C6. synonym: Df(3R)AntprA75. origin: X ray induced. references: Abbott and Kaufman, 1986, Genetics 114: 919-42. genetics: Not Antp over wild type. Complements Antp23 and Antp1. # Df(3R)Antp7 cytology: Df(3R)84B1-2;84D. origin: Induced by ethyl methanesulfonate in AntpNS. discoverer: Struhl. synonym: Df(3R)AntpNs+RC7 (Struhl, 1981; Garber et al., 1983). references: Struhl, 1981, Nature 292: 635-38. Garber, Kuroiwa, and Gehring, 1983, EMBO J. 2: 2027-36. genetics: Deficient for Antp but not for ftz or Scr (Struhl 1981; Riley, Carroll, and Scott, 1987, Genes and Development 1: 716-30). molecular biology: Proximal breakpoint 154 kb to the left of the proximal breakpoint of In(3R)Hu (Garber et al., 1983). # Df(3R)Antp17 cytology: Df(3R)84A6;84D13-14 (Baker); 84B1;84D11-12 (Lewis et al., 1980). origin: X ray induced in AntpNS. synonym: Df(3R)AntpNs+R17 (Duncan and Kaufman, 1975). references: Duncan and Kaufman, 1975, Genetics 80: 733-52. Lewis, Kaufman, and Denell, 1980, DIS 55: 85-87. Lewis, Kaufman, Denell, and Tallerico, 1980, Genetics 95: 367-81. Wakimoto, Lewis, and Kaufman, 1980, DIS 55: 140-41. Seeger, Haffley, and Kaufman, 1988, Cell 55: 589-600. genetics: Deficient for Scr-roe; includes Est-C (Ohnishi and Voelker, 1982, DIS 58: 120). Associated with dominant reduced-sex-comb phenotype. Fails to complement the recessive lethalities of ScrMsc, Antp, and Scx. Embryonic lethal with Df(3R)Scx. Male heterozygotes semisterile (Kaufman). molecular biology: Distal (84D13-14) breakpoint located at -31 kb (Baker and Wolfner; 0 point = Hind III site in (Tub84D, "+" values to the right, "-" values to the left). # Df(3R)Antp72: see In(3R)Antprv72 # Df(3R)Antp-Scx: see Df(3R)Scx2 # Df(3R)Antp-X1 cytology: Df(3R)83F4-84A1;84B1-2 + Df(3R)84B6-C1;84C5-6; defi- ciencies for two noncontiguous segments juxtaposed by In(3R)Antp73b = In(3R)84B1-2;84C5-6. new order: 61-83F4|84B6-84B2|84C6-100. origin: X-ray-induced in In(3R)Antp73b. synonym: Df(3R)Antp73b+RX1 (Cavener et al., 1986); Df(3R)Antp73b+RX3 (Hazelrigg and Kaufman, 1983). references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. Cavener, Otteson, and Kaufman, 1986, Genetics 114: 111-23. Cavener, Corbett, Cox, and Whetten, 1986, EMBO J. 5: 2939-48. genetics: Deficient for Antp; shows reduced-sex-comb phenotype. Marked with Ki. molecular biology: Distal breakpoint at about +156 kb in the molecular map of Cavener et al., 1986 (ref. #2). other information: Isolated independently of Df(3R)Antp-X2 (Hazelrigg and Kaufman, 1983). # Df(3R)Antp-X2 cytology: Df(3R)83F4-84A1;84B1-2 + Df(3R)84B6-C1;84C5-6; defi- ciencies for two noncontiguous segments juxtaposed by In(3R)Antp73b = In(3R)84B1-2;84C5-6. new order: 61-83F4|84B6-84B2|84C6-100. origin: X-ray-induced in In(3R)Antp73b. synonym: Df(3R)Antp73b+RX2 (Cavener et al., 1986); Df(3R)Antp73b+RX4 (Hazelrigg and Kaufman, 1983). references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. Cavener, Otteson, and Kaufman, 1986, Genetics 114: 111-23. genetics: Deficient for Antp; shows reduced-sex-comb phenotype. Marked with red e. # Df(3R)awd7: Deficiency (3R) abnormal wing disks. references: Biggs, Tripoulas, Dearolf, and Shearn, 1988, Genes Dev. 2: 1333-43. genetics: Deficient for awd and both flanking transcription units. # Df(3R)awd21 cytology: Deficient for 100C-D. references: Biggs, Tripoulas, Hersperger, Dearolf, and Shearn, 1988, Genes Dev. 2: 1333-43. genetics: Deficient for awd. # Df(3R)|2t: see In(3R)ScrMscLAntpBR # Df(3R)Bd: Deficiency (3R) Beaded cytology: Df(3R)97D;97F-98A. origin: X ray induced. discoverer: P. Lewis. synonym: Df(3R)Ser+82f24. genetics: Fails to complement lethality of Bd3; also slightly enhances nd on the X chromosome. Deficient for ro and Bd. # Df(3R)bxd100: Deficiency (3R) bithoraxoid cytology: Df(3R)89B5-6;89E2-3. origin: Aneuploid recombinant from Tp(3;3)bxd100/+. discoverer: E. B. Lewis. references: Struhl, 1982, Genetics 102: 737-49. genetics: Deficient for ssa, bx, and Ubx; mutant for bxd. # Df(3R)bxd110: see Tp(3;3)bxd110 # Df(3R)by: Deficiency (3R) blistery origin: X ray induced. references: Kemphues, Raff, Raff, and Kaufman, 1980, Cell 21: 445-51. Kemphues, Raff, and Kaufman, 1983, Genetics 105: 345-56. deficiency cytology genetics ____________________________________________ Df(3R)by10 85D8-12;85E7-F1 by--M(3)85E- Df(3R)by61 85D11-14;85F16 by--M(3)85E- Df(3R)by62 85D11-14;85F16 by--M(3)85E- Df(3R)by77 85D8-12;86B4 by--M(3)85E- Df(3R)by416 85D10-12;85E1-3 by- # Df(3R)c3G2 cytology: Df(3R)89A2-3;89A4-5. references: Hughes, Nelson, Yanuk, and Szauter (unpublished). genetics: Deficient for c(3)G. # Df(3R)C4 cytology: Df(3R)89E;90A. origin: X ray induced in Mcp. discoverer: Crosby. references: Kuhn, Woods, and Andrew, 1981, Genetics 99: 99- 107. Karch, Weiffenbach, Peifer, Bender, Duncan, Celniker, Crosby, and Lewis, 1985, Cell 43: 81-96. Struhl and White, 1985, Cell 45: 507-19. Casanova, Sanchez-Herrero, and Morata, 1986, Cell 47: 627-36. genetics: Deficient for iab6-iab9 (Karch et al., 1985). Includes Abd-B and is associated with slight reductions in Ubx and abd-A activity. molecular biology: Proximal breakpoint 133.5-137 kb distal to the right breakpoint of In(3R)Cbxrv1. # Df(3R)ca: Deficiency (3R) claret origin: X ray induced in Dp(3;1)B152. genetics: Deficient for ca and M(3)99B. deficiency cytology synonym ref ( ________________________________________________________ Df(3R)ca1A | 98F14;100B5-7 Dp(3;1)1A 1, 2 (Strecker) Df(3R)ca3 98F14;99E5-F1 Dp(3;1)3 1, 2 Df(3R)ca19 98F14;99F7-8 Dp(3;1)19 1 Df(3R)ca27 99B4-5;99B10-C1 Dp(3;1)27 1, 2 Df(3R)ca34 98F14;99E5-F1 Dp(3;1)34 1, 2 Df(3R)ca35 98F14;99D3-5 Dp(3;1)35 1 Df(3R)ca45B 98F14;99C1-2 Dp(3;1)45B 1 Df(3R)ca46A 98F14;99B5-9 Dp(3;1)46A 1, 2 Df(3R)ca48 98F14;100B7-8; Dp(3;1)48 1, 2 complex Df(3R)ca52 99A9-10;99C5-6 Dp(3;1)52 1 Df(3R)ca67A 98F14;99D9-E1 Dp(3;1)67A 1, 2 Df(3R)ca67N | 98F14;99D6-9 Dp(3;1)67N 1, 2 Df(3R)ca74 98F14;99C2-6 Dp(3;1)74 1, 2 Df(3R)ca78 98F14;99C5-7 Dp(3;1)78 1, 2 Df(3R)ca79 | 98F14;100B4-5 Dp(3;1)79 1, 2 (Strecker) Df(3R)ca88 98F14;99F6-8 Dp(3;1)88 1, 2 Df(3R)ca93 98F14;99F9-10 Dp(3;1)93 1, 2 Df(3R)ca97 98F14;99E1-2 Dp(3;1)97 1 Df(3R)ca124P 99A2-3;99E4-5/ Dp(3;1)124P 1, 2 Df(3R)ca138P 99B5-9;99F9-100A1 Dp(3;1)138P 1 Df(3R)ca150P 98F14;100B1-2 Dp(3;1)150P 1, 2 Df(3R)ca152P | 98F14;100A1-2 Dp(3;1)152P 1, 2 (Strecker) Df(3R)ca165P 99B2-4;99C5-6 Dp(3;1)165P 1 Df(3R)ca-L127 99B5-6;99E4-F1 Dp(3;1)L127 1 Df(3R)ca-R10 | 98F14;99D6-9 Dp(3;1)R10 1, 2 Df(3R)ca-R14 | 99A8-9;99D1-2 Dp(3;1)R14 1, 2 Df(3R)ca-R15 98F14;99F7-8 Dp(3;1)R15 ( 1 = Frisardi and MacIntyre, 1984, Mol. Gen. Genet. 197: 403- 13; 2 = Kongsuwan, Dellavalle, and Merriam, 1986, Genetics 112: 539-50. | Cytology of Frisardi and MacIntyre modified by Kongsuwan et al. / Distal break in the first intron of Mlc2 (Warmke, Kreuz, and Falkenthal, 1989, Genetics 122: 139-51). # In(3R)CA origin: / ray induced. discoverer: Ashburner. inversion cytology _______________________ In(3R)CA23 ( 81;98C In(3R)CA33 ( 81;98C In(3R)CA35 92;97 In(3R)CA37 81;84E In(3R)CA52 81;99B ( same? # Df(3R)Cha: Deficiency (3R) Choline Acetyltransferase deficiency cytology discoverer synonym ref ( genetics ____________________________________________________________________________ Df(3R)Cha1 91A1-2;91E Greenspan Def-Cat; 5, 6 Cha- Def-Cha Df(3R)Cha1a 91C2-3;91F5-92A1 Myers, Df(3R)ChaM1 1-3 Cha-- l(3)91Ff - Gelbart Df(3R)Cha2 91C7-D1;92A2 Myers, Df(3R)ChaM2 2, 3 Cha-- Dl - Gelbart Df(3R)Cha5 91B3;91D1 Gelbart, Df(3R)148.5-1 3-5 fru-- Cha- Df(3R)Cha7 91A;91F3 Myers, Df(3R)ChaM7 2-4 gl-- Cha- Gelbart Df(3R)Cha9 91C7-D1;92A2 Myers, Df(3R)ChaM9 2,4 Cha-- Dl- Gelbart Df(3R)Cha12 91A;91D1-2 + 3 Cha- In(3R)90F;100A1 ( 1 = Alton, Fechtel, Kopczynski, Shepard, Kooh, and Muska- vitch, 1989, Dev. Genet. 10: 261-72; 2 = Alton, Fechtel, Terry, Meikle, and Muskavitch, 1988, Genetics 118: 235-45; 3 = Ashburner; 4 = Gailey and Hall, Genetics 121: 773- 85; 5 = Gorczyca and Hall, 1984, J. Neurogenet. 1: 289- 313; 6 = Greenspan, 1980, J. Comp. Physiol. 137: 83-92. # Df(3R)CP1 cytology: Df(3R)84A5;84B1. references: Source of deficiency unknown, cytology from Kaufman's laboratory. # Df(3R)crb87-4 cytology: Df(3R)95F15;96A1. references: Wustmann, Szidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. genetics: Deficient for crb. # Df(3R)crb87-5 cytology: Df(3R)95F7-9;96A17-18. references: Wustmann, Szidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. genetics: Deficient for crb. # Df(3R)cu cytology: Df(3R)86C1-2;86D8. discoverer: Holden. synonym: Df(3R)cu40. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. Ohnishi and Voelker, 1982, DIS 58: 120. genetics: Deficient for Odh and cu. # Df(3R)D: Deficiency (3R) Duncan discoverer: Duncan. deficiency cytology ref ( genetics ___________________________________________________________ Df(3R)D6 84D2-3;84F11-16 1 roe-- dsx- Df(3R)D7 84D3-5;84F1-2 1 p-- dsx- Df(3R)D8 | 84D3-5;85A2-4 2 l(3)84Ef-- l(3)85Aa- ( 1 = Cavener, Otteson, and Kaufman, 1986, Genetics 114: 111-23; 2 = Jones and Rawls, 1988, Genetics 120: 733-42. | At molecular map coordinate -57 on the 85A DNA map (Jones and Rawls, 1988). # Df(3R)Dfd13: Deficiency (3R) Deformed cytology: Df(3R)83E3;84A4-5. origin: X-ray-induced reversion of Dfd. synonym: Df(3R)Dfd+RX13. references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. genetics: Reduced-sex-comb phenotype in heterozygotes. Defi- cient for Dfd, Scr and ftz but not Antp. # Df(3R)DG deficiency cytology genetics ______________________________________ Df(3R)DG1 90E1-2;91C3-7 sr-- gl- Df(3R)DG2 89E-F;91B1-2 sr-- gl- Df(3R)DG3 89F;90F sr- Df(3R)DG4 90E1-2;90F3-11 sr- Df(3R)DG5 90E-F;91E-F gl- # Df(3R)Dhod15: Deficiency (3R) Dihydroorotase cytology: {Df(3R)85A;85A}. discoverer: Rawls and Jones. references: Bender, Turner, and Kaufman, 1987, Dev. Biol. 119: 418-32. genetics: Deficient for Dhod. # Df(3R)Dipr: Deficiency (3R) Distal into proximal origin: X ray induced revertants of rnD (= Dipr). references: Kerridge, 1981, Mol. Gen. Genet. 184: 519-23. genetics: Deficient for rn. Lethal with Df(3R)Antp17. deficiency cytology synonym ______________________________________________________________ Df(3R)Dipr2 84F;84F Df(3R)Dipr4 84F;84F Df(3R)Dipr8 84F;84F Df(3R)Dipr11 84D;84F Df(3R)Dipr+R1 Df(3R)Dipr12 84D;84F Df(3R)Dipr+R2 Df(3R)Dipr15 84D;84F + In(3R)84D3-4;84F6-11 Df(3R)Dipr+R5 Df(3R)Dipr17 84D;84F Df(3R)Dipr+R7 Df(3R)Dipr19 84D;84F Df(3R)Dipr+R9 # Df(3R)Dl: Deficiency (3R) Delta deficiency cytology origin discoverer ref ( genetics _______________________________________________________________________________ Df(3R)Dl1 90D2-4;92A1-2 spont Schultz 4 Dl- Df(3R)Dl2 91D3;92A1-2 X ray Myers Dl- Df(3R)Dl5 | 91F5-13;92E1-11 X ray 5,7 Dl-- tRNA - val3b- Df(3R)Dl12 91F6-13;92A1 spont Bridges 2 Dl- Df(3R)Dl-A143 91F13;92A2-3 HD Tepass 8 Dl- Df(3R)Dl-BX6 92A1-2 X ray 1 Dl- Df(3R)Dl-BX12 91F1-2;92D3-6 X ray Muskavitch 1, 2 l(3)91Fb-- Dl- Df(3R)Dl-FX2 91D3;92A5-8 X ray 6,8 Dl- Df(3R)Dl-FX3 91F11;92A3 X ray 6,8 Dl- *Df(3R)Dl-H 91C6-D1;92A2-3 chemical Auerbach 3, 4 Dl- Df(3R)Dl-HD28 91F6-13;92A2-3 HD 1, 2 l(3)91Fd-- Dl- Df(3R)Dl-KX4 92A2;92B3-10 X ray Dl- Df(3R)Dl-KX5 91C;92E X ray Vassin 8 Dl- Df(3R)Dl-KX9 91F6-10;92B4-8 X ray Vassin 8 Dl- Df(3R)Dl-KX10 91F6-10;92B X ray De la Concha 8 Dl- Df(3R)Dl-KX12 92A2;92A + X ray Vassin 8 Dl- In(3)67C-D;92A2 Df(3R)Dl-KX16 91C;92B11-C1 X ray Vassin 8 Dl- Df(3R)Dl-KX17 91F10-13;92E X ray Vassin 8 Dl- Df(3R)Dl-KX18 91F13-92A1; X ray Vassin 8 Dl- 92D7-E3 Df(3R)Dl-KX20 91F1-5;92A2 X ray Vassin 8 Dl- Df(3R)Dl-KX21 91F3;92A2 X ray Vassin 8 Dl- Df(3R)Dl-KX23 91C7-D3;92A5-8 X ray Vassin 8 Dl- Df(3R)Dl-KX24 91A1-2;92B9-11 X ray Vassin 8 Dl- Df(3R)Dl-M2 91C7-D1;93A1 Myers, 2 Dl- Gelbart Df(3R)Dl-P 91F10;92B3 HD Vassin 8 Dl- Df(3R)Dl-PX 91D1;92A7 X ray Vassin 6, 8 Dl- Df(3R)Dl-X43 91F11;92A8-10 X ray Campos- 2, 6, 8 Dl- Ortega ( 1 = Alton, Fechtel, Kopczynski, Shepard, Kooh, and Muska- vitch , 1989, Dev. Genet. 10: 261-72; 2 = Alton, Fechtel, Terry, Meikle, and Muskavich, 1988, Genetics 118: 235-45; 3 = CP627; 4 = Auerbach, 1943, DIS 17: 49; 5 = Larson, Miller, Spiegelman, Hayashi, Tener, Sinclair, and Grigli- atti, 1982, Mol. Gen. Genet. 185: 390-96; 6 = Lehmann, Jimenez, Dietrich, and Campos-Ortega, 1983, Wilhelm Roux's Arch. Dev. Biol. 192: 62-74; 7 = Scavarda, O'Tousa, and Pak, 1983, Proc. Nat. Acad. Sci. USA 80: 4441-45; 8 = Vas- sin and Campos-Ortega, 1987, Genetics 116: 433-45. | Also deficient for ninaE (Larson et al., 1982). # Df(3R)dsx: Deficiency (3R) doublesex origin: X ray induced. genetics: Revertants of dominant alleles at the dsx locus affecting chromosomally female flies. deficiency cytology synonym ( ref | _________________________________________________________________ Df(3R)dsx1 84D6-7;85A1-3 Df(3R)dsxD+R1 4 Df(3R)dsx2D 84D11;84F16 Df(3R)dsxD+R2 4 Df(3R)dsx2M / 84C1-3;84E1 Df(3R)dsxMas+R2 1, 3 (Baker) Df(3R)dsx3 84D11-14;84E12-13 Df(3R)dsxMas+R3 1 Df(3R)dsx5 ` 84E1-2;84F11-12 Df(3R)dsxD+R5 2, 4 Df(3R)dsx8 - 84D13-14;85A1-3 Df(3R)dsxD+R8 2 Df(3R)dsx10D - 84D11-12;85A1-3 Df(3R)dsxD+R10 6 Df(3R)dsx10M 84D3;84F1-2 Df(3R)dsxMas+R10 1 Df(3R)dsx11 84D8-9;85A1-3 Df(3R)dsxMas+R11 1, 5 Df(3R)dsx15 84D11;84E8 Df(3R)dsxMas+R15 1 Df(3R)dsx21 84D11-12;84E8 Df(3R)dsxMas+R21 1 Df(3R)dsx27 84D9 (within); 85A1-3 Df(3R)dsxMas+R27 1 (near distal edge) Df(3R)dsx28 84D13-E1;85A4-5 Df(3R)dsxMas+R28 1 Df(3R)dsx29 84C8-D1 (interband); Df(3R)dsxMas+R29 1, 3 84F6-7 (within) Df(3R)dsx33 n 84D10-11 (interband); Df(3R)dsxMas+R33 1 85A1-3 (distal edge) Df(3R)dsx34 84D3-4;85B4-5 Df(3R)dsxMas+R34 1 Df(3R)dsx37 84D8;85B3-5 Df(3R)dsxMas+R37 1 Df(3R)dsx43 84D13-14;84E6-8 Df(3R)dsxMas+R43 1 Df(3R)dsx48 see In(3R)dsx48 ( Original strain (dsxD or dsxMas) indicated in superscript. | 1 = Baker, Hoff, Kaufman, Wolfner, and Hazelrigg, 1991, Genetics 127: 125-38; 2 = Baker and Ridge, 1980, Genetics 94: 383-423; 3 = Cavener, Corbett, Cox, and Whetten, 1986, EMBO J. 5: 2939-48; 4 = Duncan and Kaufman, 1975, Genetics 80: 733-52; 5 = Jones and Rawls, 1988, Genetics 120: 733- 42; 6 = Kaufman. / Proximal (84C1-3) breakpoint estimated to be at about +26 to +27 kb, based on location of 84C1-2 breaks of T(2;3)Ta1 at +34 kb and Df(3R)Scx2 at +41 kb (Baker and Wolfner, 1988, Genes Dev. 2: 477-89). Also deficient for hat and nac. ` Part of 84E1-2 fused with part of 84F11-12. Proximal break- point at about -4kb on the molecular map of Cavener et al., 1986. - Deficient for Su(var)304 as well as dsxD (Reuter, Dorn, Wustmann, Friede, and Rauh, 1986, Mol. Gen. Genet. 202: 481-87). Broken within 85A1-3, deleting centromere proximal but not centromere distal material (B.S. Baker; Jones and Rawls, 1988). n Proximal breakpoint at about +134 kb on the molecular map of Cavener et al., 1986. # Df(3R)e: Deficiency (3R) ebony origin: Df(3R)e-G chromosomes were / ray induced, other defi- ciencies X ray induced. deficiency cytology ref ( genetics _______________________________________________________________________ *Df(3R)e4.39 93B;93F 1 e- Df(3R)e67l 93B5-7;93D3 6 e- *Df(3R)e100.172 93B7-19;93F10-94A1 12 e- *Df(3R)e100.256 93A5-B1;93F5-9 12 e- Df(3R)e-B52 93C3-6;93F5-8 Df(3R)e-D7 | 93C3-6;93F6-8 2, 3, 7, l(3)93Cb-- l(3)93Fa- 8, 10, 11 Df(3R)e-F1 93B6-7;93E1-2 4, 7, 8, l(3)93Cb-- l(3)93Di- 10, 11 Df(3R)e-F2 | 93A6-B1;93D7-10 4, 7, l(2)93Ba-- l(3)93Dh- 8, 10 Df(3R)e-F3 | 93B8-13;93E6-11 4, 7, l(3)93Ba-- l(3)93Dj- 8, 10 Df(3R)e-F4 | 93C3-6;93F11-14 4, 7, l(3)93Ca-- l(3)93Fc- 8, 10 Df(3R)e-GC3 93C3-6;94A 7, 8 l(3)93Cb-- l(3)93Fc- Df(3R)e-GC9 93B11-13;93D9-10 7, 8 l(3)93Ba-- l(3)93Dh- Df(3R)e-Gp4 93B11-13;93D7-9 7, 8 l(3)93Ba-- Hsr93D- Df(3R)e-H4 / 93C3-6;93F6-8 7, 8 l(3)93Cc-- l(3)93Fc- Df(3R)e-H5 / 93B11-13;93D4-6 5, 7, 8 l(3)93Ba-- l(3)93Da- Df(3R)e-H6 / 93C3-6;94A 7, 8 l(3)93Cb-- l(3)93Fc- Df(3R)e-N19 93B;94 11 e- Df(3R)e-N26 93B;93F 11 l(3)93Ba-- e- Df(3R)e-R1 ` 93B3-5;93D2-4 7, 8, 9 l(3)93Ba-- e- Df(3R)e-R6 ` 93B4-5;94A5-16 9 e- ( 1 = Alexander, 1960, Genetics 45: 1019-22; 2 = Caggese, Caizzi, Morea, Scalenghe, and Ritossa, 1979, Proc. Nat. Acad. Sci. USA 76: 2385-89; 3 = D'Alessandro, Ritossa, and Scalenghe, 1977, DIS 52: 46; 4 = Fortebracchio, Scalenghe, and Ritossa, 1977, DIS 52: 102; 5 = Henikoff, 1980, DIS 55: 61-62; 6 = Korge, 1972, DIS 48: 20; 7 = Mohler and Pardue, 1982, Chromosoma 86: 457-67; 8 = Mohler and Pardue, 1984, Genetics 106: 249-65; 9 = Rawls, 1980, Mol. Gen. Genet. 178: 43-49; 10 = Scalenghe and Ritossa, 1976, Atti Accad. Naz. Lincei 13: 439-528; 11 = Scalenghe and Ritossa, 1977, Chromosoma 63: 317-26; 12 = Ward and Alexander, 1957, Genetics 42: 42-54. | Cytology according to Mohler and Pardue, 1984 (different breakpoints given by Scalenghe and Ritossa, 1977). / Discovered by S. Henikoff. ` Discovered by B.S. Baker. # Df(3R)E45 cytology: Df(3R)100C5;100F. origin: P-element induced mutagenesis. references: Locke, Kotarski, and Tartof, 1988, Genetics 120: 181-98. genetics: Enhances position-effect variegation in In(1)wm4. # Df(3R)E79 cytology: Df(3R)86F1-2;87B8-10 (Gausz). origin: Induced by ethyl methanesulfonate. references: Gausz, Gyurkovics, Bencze, Awad, Holden, and Ish- Horowicz, 1981, Genetics 98: 775-89. Ohnishi and Voelker, 1981, Biochem. Genet. 19: 75-85. genetics: Deficient for Dip-C and l(3)86Fa - l(3)87Bg. Lacks heat shock puff site at 87A7. # Df(3R)E229 cytology: Df(3R)86F6-7;87B1-2 (Gausz). origin: Induced by ethyl methanesulfonate. synonym: Df(3R)229 (Ish-Horowicz and Pinchin, 1980). references: Ish-Horowicz, Pinchin, Gausz, Gyurkovics, Bencze, Goldschmidt-Clermont, and Holden, 1979, Cell 17: 565-71. Ish-Horowicz and Pinchin, 1980, J. Mol. Biol. 142: 231-45. Gausz, Gyurkovics, Bencze, Awad, Holden, and Ish-Horowicz, 1981, Genetics 98: 775-89. Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95. genetics: Deficient for l(3)86Fe - l(3)87Ae. Lacks heat shock puff site at 87A7. Uncovers sad (Jurgens et al., 1984). # Df(3R)E307 cytology: Df(3R)87B2-4;87D1-2 (Gausz). origin: Induced by ethyl methanesulfonate. references: Gausz, Gyurkovics, Bencze, Awad, Holden, and Ish- Horowicz, 1981, Genetics 98: 775-89. genetics: Deficient for Dip-C - l(3)87Bg. Lacks heat shock puff site at 87C1. # Df(3R)ea: Deficiency (3R) easter cytology: Df(3R)88E7-13;89A1. origin: Induced by hybrid dysgenesis. references: Chasan and Anderson, 1989, Cell 56: 591-600. genetics: Fertile revertant of dominant easter allele. # Df(3R)Espl: Deficiency (3R) Enhancer of split genetics: Deficient for E(spl). deficiency cytology origin synonym ref ( _____________________________________________________________________ Df(3R)Espl1 96F7;97A6 X ray E(spl)8D06 1 Df(3R)Espl2 In(3R)96C3-9;96E5-12;97A3-4 X ray E(spl)A7.13.2 2 (deficient for 96E5;97A4) Df(3R)Espl3 | 96F1;97B1 E(spl)BX36 4 Df(3R)Espl4 96F8-9;96F12-13 X ray E(spl)RB25.1 2 Df(3R)Espl5 In(3R)96F2;96F12-14;99C E(spl)R1 3 (deficient for 96F12-14) Df(3R)Espl6 96F5;97A9-10 X ray E(spl)R2 3 Df(3R)Espl7 96F9;97A4-6 X ray E(spl)R3 3 Df(3R)Espl8 96F9-10;97A6-10 X ray E(spl)R23.1 2 Df(3R)Espl9 / 96F5-7;96F12-14 X ray l(gro)X1 4 Df(3R)Espl10 / 96F5-7;97B1 X ray l(gro)X72 4 ( 1 = Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Roux's Arch. Dev. Biol. 93: 283-95; 2 = Knust, Bremer, Vas- sin, Ziemer, Tepass, and Campos-Ortega, 1987, Dev. Biol. 122: 262-73; 3 = Lehmann, Dietrich, and Campos-Ortega, 1985, J. Neurogenet. 2: 291-308; 4 = Preiss, Hartley, and Campos-Ortega, 1988, EMBO J. 7: 3917-27. | Discoverer: Muskavitch. / Discoverer: Preiss. # Df(3R)F76 cytology: {Df(3R)84F;84F}. genetics: roe- - rn-. # Df(3R)fs293 cytology: Df(3R)?;88A1-2. genetics: Deficient for ems. # Df(3R)G1 cytology: Df(3R)85A4-5;85A6-11. discoverer: Porter. references: Bender, Turner, and Kaufman, 1987, Dev. Biol. 119: 418-32. Jones and Rawls, 1988, Genetics 120: 733-42. genetics: Deficient for Dhod, p, l(3)85Ac-l(3)85Ag. molecular biology: DNA coordinates of the 85A proximal break- point and the 85A distal breakpoint are -49 and +45 respec- tively ("+" values to the right and "-" values to the left or centromere end of map). # Df(3R)GB14 cytology: Df(3R)85D12;85E10. # Df(3R)GB104 cytology: Df(3R)85D11-13;85E10. genetics: Deficient for ( Tub85E. # Df(3R)GC14 cytology: {Df(3R)93D6-7;93D9-10}. origin: / ray induced. references: Mohler and Pardue, 1982, Chromosoma 86: 457-67. 1984, Genetics 106: 249-65. genetics: Deficient for Hsr-93D and l(3)93Dh. # Df(3R)GE origin: X ray induced loss of TE88A. references: Gausz, Hall, Spierer, and Spierer, 1986, Genetics 112: 65-78. deficiency cytology genetics DNA breakpoints (proximal) ( _____________________________________________________________________ Df(3R)GE26 87E1-2 -30, -23 Df(3R)GE41 | 87E4 Ace+ l(3)87Ee-- l(3)87Ef- +56.5, +58.8 Df(3R)GE99 87E1-2 ( ry-Ace walk, "+" values to right, "-" values to left (Gausz et al., 1986). | Other molecular references: Hall and Spierer, 1986, EMBO J. 5: 2949-54; Nagoshi and Gelbart, 1987, Genetics 117: 487-502; Fournier, Karch, Bride, Hall, Berge, and Spierer, 1989, J. Mol. Biol. 210: 15-22. # Df(3R)gl: Deficiency (3R) glass deficiency cytology genetics ______________________________________________ Df(3R)gl-BX1 90F8-11;91B1-2 sr+gl-- fru- Df(3R)gl-BX5 91B1-2;91D1-2 Df(3R)gl-BX6 90C9-10;90F2-11 sr-gl+ Df(3R)gl-BX10 90C7-8;91B1-2 sr-- fru- # Df(3R)gro: Deficiency (3R) groucho genetics: Deficient for E(spl). deficiency cytology ______________________________ Df(3R)gro-X1 96F5-7;96F12-14 Df(3R)gro-X2 96F5-7;97B1 # Df(3R)H5: see Df(3R)kar-H5 # Df(3R)H10: see Df(3R)kar-H10 # Df(3R)H13: see Df(3R)kar-H13 # Df(3R)H-B79 cytology: Df(3R)92B3-11;92F8-13. references: Wustmann, Szidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. Bang, Hartenstein, and Posakony, 1991, Development 111: 89- 104. genetics: Deficient for H. # Df(3R)hh: Deficiency (3R) hedgehog cytology: Df(3R)92F11-14;94E2-5. origin: / ray induced. synonym: Df(3R)hh-GR2. references: Mohler, 1988, Genetics 120: 1061-72. genetics: Deficient for hh. # Df(3R)Hu: Deficiency (3R) Humeral cytology: Df(3R)84A6-B1;84B3-6 + Df(3R)84D4-5;84F1-2; deficien- cies for two non-contiguous deletions juxtaposed by In(3R)Hu. new order: 61 - 84A6|84D4 - 84B6|86C5 - 84F2|86C6 - 100. origin: Induced by ethyl methanesulfonate in In(3R)Hu. synonym: Df(3R)HurvX1; Df(3R)Hu+RX1. references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. Cavener, Otteson, and Kaufman, 1986, Genetics 114: 111-23. genetics: Deficient for Antp and Hu but not ftz. Male heterozy- gote shows reduced sex comb phenotype. molecular biology: Proximal end of the deficiency at +88; "+" values to the right, "-" values to the left. (Scott, Weiner, Hazelrigg, Polisky, Pirrotta, Scalenghe, and Kaufman, 1983, Cell 35: 763-76). # Df(3R)I9 cytology: Df(3R)92B1-3;92C1-3. genetics: Deficient for l(3)SB65. # Df(3R)JK6: see Df(3R)urd # Df(3R)K9 cytology: Df(3R)91B1-5;92C3-D1. genetics: Deficient for l(3)SB65. # In(3R)kar: Inversion (3R) karmoisin genetics: Mutant or deficient for kar. inversion cytology ref ( ________________________________________________________ In(3R)kar3H | 81;87C7-D1 + 4 84E;98F + 89B;94A In(3R)karD / 81F1;87C8 1 In(3R)karH4 87C8;89E 1 In(3R)karH6 81;87B6;87C8; 1 deficient for 87B6-C8 In(3R)karlG27 87B3-5;87D6-12;99E1-F1; 2,3 deficient for 87B3-5 to 87B6-12. ( 1 = Henikoff, 1979, Genetics 93: 105-15; 2 = Hilliker, Clark, Chovnick, and Gelbart, 1980, Genetics 95: 95-110; 3 = Hilliker, Clark, Gelbart, and Chovnick, 1981, DIS 56: 65-72; 4 = Holden. | 61A - 81|87C7 - 84E|98F - 94A|89B - 94A|89B - 87D1|81 - 84E|98F - 100F. / Homozygotes show reduced viability and male sterility; eyes vary in color from orange to brown. Heterozygotes with In(3R)karH4 fully viable. # Df(3R)kar-D origin: X ray induced in In(3R)AFA = In(3R)86C;93D6-7 chromo- some. deficiency cytology ref ( genetics ____________________________________________________________________________ Df(3R)kar-D1 |,/ 87A7-8;87D1-2 1, 2, 3, 4, 5, 6, 7 Dip - C-- kar- Df(3R)kar-D2 / 87A6-7;87D4-5 1, 2, 5, 6, 7 Dip - C-- Men- Df(3R)kar-D3 ` 86E16-18;87D3-4 2, 3, 4, 6, 7 l(3)87Ac-- Men- Df(3R)kar-D4 87B11-C2;87E12-F1 2,6 kar- ( 1 = Caggese, Caizzi, Morea, Scalenghe, and Ritossa, 1979, Proc. Nat. Acad. Sci. USA 76: 2385-89; 2 = Costa, Ritossa, and Scalenghe, 1977, DIS 52: 140; 3 = Gausz, Gyurkovics, Bencze, Awad, Holden, and Ish-Horowicz, 1981, Genetics 98: 775-89; 4 = Ish-Horowicz, Pinchin, Gausz, Gyurkovics, Bencze, Goldschmidt-Clermont, and Holden, 1979, Cell 17: 565-71; 5 = Ohnishi and Voelker, 1981, Biochem. Genet. 19: 75-85; 6 = Scalenghe and Ritossa, 1976, Atti Acad. Naz. Lincei 13: 439-528; 7 = Voelker, Ohnishi, Langley, Gausz, and Gyurkovics, 1981, Biochem. Genet. 19: 525-34. | Two deficiencies [Df(3R)kar-D1 and Df(3R)kar-D2] thought to be identical and listed separately through stock error according to Caggese et al., 1979. / Partial deletion of Hsp70 site at 87A producing 40 kb Hsp70 (Ish-Horowicz and Pinchin, 1980, J. Mol. Biol. 142: 231- 45). Lacks Hsp70 site at 87C1. ` Lacks 87A7 and 87C1 heat shock puff sites. Uncovers sad (Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95). # Df(3R)kar-H origin: X ray induced. deficiency cytology ref ( genetics ________________________________________________________________ Df(3R)kar-H1 | 87A10;87D11 1, 3 Hsp70-- kar- Df(3R)kar-H2 | 87B3;87D1-4 1 Hsp70-- kar- Df(3R)kar-H3 87C2-3;87D3-4 1 kar- Df(3R)kar-H5 | 87A1-2;87D5-7 1, 3, 4 l(3)87Aa-- kar- Df(3R)kar-H6 87B6;87C8 2 Dip - C-- kar- Df(3R)kar-H9 / 86F4;87F11 1 Hsp70-- kar- Df(3R)kar-H10 | 87A1-2;87D6-7 1, 2, 3, 4 svp-- kar- Df(3R)kar-H11 | 87B10;87F4 1, 3 Hsp70-- kar- Df(3R)kar-H12 | 87C7;87F1-2 1 kar- Df(3R)kar-H13 | 87B1-2;87D14-E1 1, 2, 4 Dip - C-- kar- Df(3R)kar-H14 / 86F10-11;87D1-2 1, 2 Dip - C-- kar- ( 1 = Henikoff, 1979, Genetics 93: 105-15; 2 = Ohnishi and Voelker, 1981, Biochem. Genet. 19: 75-85; 3 = Gausz, Gyur- kovics, Bencze, Awad, Holden, and Ish-Horowicz, 1981, Genet- ics 98: 775-89; 4 = Gausz, Hall, Spierer, and Spierer, 1986, Genetics 112: 65-78. | Lacks 87C1 heat shock puff site. / Lacks 87A7 and 87C1 heat shock puff sites. # Df(3R)kar-lG27 cytology: Df(3R)87B5;87D6 (Hilliker et al., 1980). discoverer: Gelbart. references: Hall and Kankel, 1976, Genetics 83: 517-35. Hilliker, Clark, Chovnick, and Gelbart, 1980, Genetics 95: 95-110. Hilliker, Clark, Gelbart, and Chovnick, 1981, DIS 56: 65-72. Spierer, Spierer, Bender, and Hogness, 1983, J. Mol. Biol. 168: 35-50. genetics: Deficient for kar-87De; includes Men. Lacks heat shock puff site at 87C1. molecular biology: 87D breakpoint between 184 and 191 kb to the left of the left breakpoint of In(3R)Cbxrv1 (Spierer et al., 1983; Hogness, 1983, J. Mol. Biol. 168: 17-33). # Df(3R)kar-Sz origin: X ray induced. deficiency cytology ref ( genetics ______________________________________________________________________ Df(3R)kar-Sz5 | 86E20-F1;87F3-4 1 Hsp70-- kar- Df(3R)kar-Sz8 87C1-2;87D14-E1 1, 5, 6 kar- Df(3R)kar-Sz11 / 87C7-8;87E5-6 1, 2, 4, kar-- l(3)87Ee-; 7, 8 includes Men Df(3R)kar-Sz12 ` 87B1-3;87C8-9 1, 2, 3 l(3)87Ca-- kar- Df(3R)kar-Sz13 | 86E6-7;87C8-D1 1 Hsp70-- kar- Df(3R)kar-Sz15 ` 87B1-2;87E1-2 1, 3 Hsp70-- kar- Df(3R)kar-Sz16 - 87C2;87C9-D1 1, 5, 6, 8 kar-- Men- Df(3R)kar-Sz21 87C7;87C8-9 1, 2 l(3)87Cc-- kar- Df(3R)kar-Sz23 ` 86E6-7;87C9-D1 1 Hsp70-- kar- Df(3R)kar-Sz27 87C7;87F1 1, 2 kar-- ry- Df(3R)kar-Sz28 87C7-8;87E9-10 1 kar- Df(3R)kar-Sz29 87C3-4;87C9-D1 1, 2 l(3)87Ca-- l(3)87Cd- Df(3R)kar-Sz30 ` 87B2-4;87D2-3 1, 8 Hsp70-- Men- Df(3R)kar-Sz31 | 86C6-7;87C9-D1 1, 2 l(3)87Cc-- kar- Df(3R)kar-Sz33 87C1-2;87E4-5 1 kar- Df(3R)kar-Sz37 87C5-6;87D14-E1 1, 2 l(3)87Cb-- pic- Df(3R)kar-Sz40 ` 87B2-3;87D1-3 1 Hsp70-- kar- Df(3R)kar-Sz72 87E1-3;87F13-14 1 kar- ( 1 = Gausz, Awad, and Gyurkovics, 1980, DIS 55: 45-46; 2 = Gausz, Bencze, Gyurkovics, Ashburner, Ish-Horowicz, and Holden, 1979, Genetics 93: 917-34; 3 = Gausz, Gyurkovics, Bencze, Awad, Holden, and Ish-Horowicz, 1981, Genetics 98: 775-89; 4 = Hilliker, Clark, Gelbart, and Chovnick, 1981, DIS 56: 65-72; 5 = Ish-Horowicz and Pinchin, 1980, J. Mol. Biol. 142: 231-45; 6 = Ish-Horowicz, Pinchin, Gausz, Gyurkovics, Bencze, Goldschmidt-Clermont, and Holden, 1979, Cell 17: 565-71; 7 = Spierer, Spierer, Bender, and Hogness, 1983, J. Mol. Biol. 168: 35-50; 8 = Voelker, Ohnishi, Lang- ley, Gausz, and Gyurkovics, 1981, Biochem. Genet. 19: 525- 34. | Lacks 87A7 and 87C1 heat shock puff sites. / Molecular coordinates of distal breakpoint between +82 and +93 (Spierer et al., 1983). ` Lacks 87C1 heat shock puff site. - Broken within Hsp70 at 87C1; heat shock protein small (Ish- Horowicz and Pinchin, 1980). Survives 20 minutes of heat shock at 40.5 if given pretreatment for 30 minutes at 33-35 [Mitchell, Moller, Peterson, and Lipps-Sarmiento, 1979, Dev. Genet. 1: 181-92]. Distal to kar (at 87C8 according to Gausz et al., 1981). # Df(3R)Kx1 cytology: Df(3R)86C1;87B5. discoverer: Vassin. references: Reuter, Gausz, Gyurkovics, Friede, Bang, Spierer, Hall, and Spierer, 1987, Mol. Gen. Genet. 210: 429-36. genetics: Dominant suppressor of wm4h variegration. # Df(3R)L16 cytology: Df(3R)96A1-10;96E. origin: X ray induced. references: Gonzales, Molina, Casal, and Ripoll, 1989, Genetics 123: 371-77. genetics: Practically lethal over asp in late larvae, with mitotic abnormalities of the brain identical to those of Df(3R)Su9/asp larvae; Df(3R)Su9/TM6B larval brains normal. Escapers [Df(3R)L16/asp] are Minute, showing cuticular defects and male and female sterility. # Df(3R)l26c cytology: Df(3R)87D14-E1;87F11-12 (Gelbart, Lefevre). discoverer: Chovnick. discoverer: Gelbart. references: Hall and Kankel, 1976, Genetics 83: 517-35. Hilliker, Clark, Chovnick, and Gelbart, 1980, Genetics 95: 95-110. Hilliker, Chovnick, and Clark, 1981, DIS 56: 64-72. Spierer, Spierer, Bender, and Hogness, 1983, J. Mol. Biol. 68: 35-50. Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95. genetics: Deficient for l(3)87Eb to region distal to l(3)87Ek. Uncovers yrt (Jurgens et al., 1984). molecular biology: Molecular coordinates of proximal breakpoint between -129 and -115 (Spierer et al., 1983). # Df(3R)l26d cytology: Df(3R)87D11-13;87E3-5 (Gelbart, Hilliker, Lefevre). discoverer: Chovnick. references: Hall and Kankel, 1976, Genetics 83: 517-35. Hilliker, Clark, Chovnick, and Gelbart, 1980, Genetics 95: 95-110. Hilliker, Chovnick, and Clark, 1981, DIS 56: 64-72. Spierer, Spierer, Bender and Hogness, 1983, J. Mol. Biol. 68: 35-50. Nagoshi and Gelbart, 1987, Genetics 117: 487-502. genetics: Deficient for pic-l(3)87Ef (includes Ace). molecular biology: Molecular coordinates of distal breakpoint between +79.5 and +90.5, of proximal breakpoint between -160.5 and -157.5 (Spierer et al., 1983). # Df(3R)lC4a cytology: Df(3R)87E5-7;87E11-F1 (Gelbart). discoverer: Chovnick. references: Hall and Kankel, 1976, Genetics 83: 517-35. Hilliker, Clark, Chovnick, and Gelbart, 1980, Genetics 95: 95-110. Hilliker, Chovnick, and Clark, 1981, DIS 56: 64-72. Spierer, Spierer, Bender, and Hogness, 1983, J. Mol. Biol. 68: 35-50. genetics: Deficient for l(3)87Eg-l(3)87Ej. molecular biology: Molecular coordinates of proximal breakpoint between +73 and +85 (Spierer et al., 1983). # Df(3R)LIN cytology: Df(3R)84A4-5;84B1-2. origin: Induced by ethyl methanesulfonate. references: Frohnhofer and Nusslein-Volhard, 1986, Nature (Lon- don) 324: 120-25. Pultz, Diederich, Cribbs, and Kaufman, 1988, Genes Dev. 2: 901-20. genetics: Deficient for bcd. # Df(3R)M1: Deficiency (3R) of Morata discoverer: Casanova and Morata. references: Sanchez-Herrero, Vernos, Marco, and Morata, 1985, Nature 313: 108-13. Casanova, Sanchez-Herrero, and Morata, 1986, Cell 47: 627-36. genetics: Deficient for the entire BXC and l(3)89Ea, but not l(3)89Ee. # Df(3R)M86D: Deficiency (3R) Minute cytology: Df(3R)86D1-2;86D4 (Ashburner et al., 1980). origin: X ray induced. discoverer: Schultz, 33a10. synonym: Df(3R)M-S31. references: 1940, DIS 13: 51. Ashburner, Richards, and Velissariou, 1980, DIS 55: 196. genetics: Deficient for Odh, M(3)86D, cu, neu (Clark, 1983, Biochem. Genet. 21: 375-90). # Df(3R)M-S31: see Df(3R)M86D # Df(3R)M95A cytology: Df(3R)94D;95A3. origin: X ray induced. synonym: Df(3R)MSu244. references: Reuter, Dorn, Wustmann, Friede, and Rauh, 1986, Mol. Gen. Genet. 202: 481-87. genetics: Deficient for M(3)95A and Su(var)3-11. # Df(3R)M96A cytology: Df(3R)95E6-8;96A1-5. origin: Recombination between elements of T(Y;3)H173 = T(Y;3)95E6-8 and T(Y;3)G73 = T(Y;3)96A1-5. references: Gonzales, Molina, Casal, and Ripoll, 1989, Genetics 123: 371-77. genetics: Deficient for M(3)96A. Haplo-insufficient. Hetero- zygotes are Minute showing full penetrance and expressivity for the thin bristle phenotype. # Df(3R)MAP origin: X ray induced. deficiency cytology ref ( genetics ____________________________________________________________ Df(3R)MAP2 | 84A1-2;84A4-5 2 lab- pb- zen+ Df(3R)MAP8 / ` 84A4-5;84A4-5 1-3 lab+ pb- zen+ Df(3R)MAP11 1-3 zen- bcd- ama- Dfd- Df(3R)MAP13 ` 84A4-5;84A4-5 lab+ pb- zen+ Df(3R)MAP117 3 zen- - Antp- (and beyond) ( 1 = Diederich, Merrill, Pultz, and Kaufman, 1989, Genes Dev. 3: 399-414; 2 = Pultz, Diederich, Cribbs, and Kaufman, 1988, Genes Dev. 2: 901-20; 3 = Seeger, Haffley, and Kauf- man, 1988, Cell 55: 598-600. | Distal breakpoint at -54 kb on molecular map of the ANTC complex (Pultz et al., 1988). / Distal breakpoint at -50kb and proximal breakpoint at -110 kb on molecular map of the ANTC complex (Pultz et al., 1988). ` Synonyms: Df(3R)pb-map8 and Df(3R)pb-map13. # Df(3R)Mg28: Deficiency (3R) Mglinetz cytology: Df(3R)87D;87F. origin: / ray induced. references: Mglinetz, 1972, Genetika (Moscow) 8(2): 82-92. # Df(3R)Mg32 cytology: Df(3R)98F;100C. origin: / ray induced. references: Mglinetz, 1972, Genetika (Moscow) 8(2): 82-92. # Df(3R)ML457 cytology: Df(3R)87A;87C. origin: X ray induced. references: Mukhina and Zhimulev, 1980, DIS 55: 209. # Df(3R)MSu2: Deficiency (3R) Minute Suppressor cytology: Df(3R)100F3-5. origin: X ray induced. references: Reuter, Dorn, Wustmann, Friede, and Rauh, 1986, Mol. Gen. Genet. 202: 481-87. genetics: Exhibits a Minute phenotype and dominant suppression of variegated-type position effect. other information: The genetic map position and the inferred moderate phenotype are at odds with the location of the defi- ciency at 100F3-5. # Df(3R)MSu244: see Df(3R)M95A # Df(3R)N origin: X ray induced. references: Gausz, Hall, Spierer, and Spierer, 1986, Genetics 112: 65-78. Nagoshi and Gelbart, 1987, Genetics 117: 487-502. deficiency cytology genetics _________________________________ Df(3R)N40 87E1-2 l(3)87Ec- Df(3R)N42 87E4 Ace- Df(3R)N63 87E5-6 l(3)87Ee- Df(3R)N69 87D14-E1 sim- Df(3R)N74 87D13-14 pic- Df(3R)N78 87E4 Ace- # Df(3R)Na: see In(3R)Na # Df(3R)o: Deficiency (3R) opsin origin: / ray induced. discoverer: O'Tousa. deficiency cytology ref ( genetics ________________________________________________________ Df(3R)o11 Df(3R)92B5-6;92B7-8 1 ninaE- Df(3R)oB16 Df(3R)92A12-B1;92E7-15 2 ninaE-ort+ Df(3R)oF4 Df(3R)92A1-3;92D5-9 2 ninaE-ort- ( 1 = O'Tousa, Baehr, Martin, Hirsh, Pak, and Applebury, 1985, Cell 40: 839-50; 2 = O'Tousa, Leonard, and Pak. # Df(3R)O5: see Tp(3;1)O5 # Df(3R)p: Deficiency (3R) pink genetics: Deficient for p. discov. or molec. deficiency cytology origin ref ( biol. | ______________________________________________________________ Df(3R)p4 84D6-10;85A1-2 X ray 4, 5 + T(2;3)34D;85A1-2 Df(3R)p5 MR 1, 2 +24 - +29 Df(3R)p7 {85A;85A} 1, 2 Df(3R)p13 / ` 84F2;85B1 X ray 1, 4, 5, 8 Df(3R)p16 {85A;85A} MR 1, 2 +24 - +45 Df(3R)p17 {85A;85A} 1, 2 Df(3R)p19 {85A;85A} MR 1, 2 +24 - +33 Df(3R)p21 84F4-6;85C4-6 X ray 4, 5 Df(3R)p25 ` 85A5-7;85A11 X ray 1, 4, 5 +60 Df(3R)p30 ` 84F8-10;85D3-5 X ray 4, 5 (B.S. Baker) Df(3R)p40 ` 84E8-9;85B6 + X ray 4, 5 In(3LR)64;90 + T(2;3)55;75 Df(3R)p46 84D4-6;85D6 X ray 4, 5 Df(3R)p66 - 84D4-6;85B6-C1 + T(2;3)25D;84D4-6 + T(2;3)25D;85B6-C1 Df(3R)p118 - 84F;85A Df(3R)p712 84D4-6;85B6 + X ray 4 T(2;3)25D;85B Df(3R)p819 85A3;85B6 + X ray 4 T(2;3)41;87C + Tp(3;3)64F;67F;97 Df(3R)p-bs12 85A;? Df(3R)p-bs13 85A;? Df(3R)p-XM66 - 85A3;85B6 3 Df(3R)p-XT6 85A3;85C1-2 Df(3R)p-XT9 - 84F14;85C-D X ray 7 Df(3R)p-XT15 {85A;85A} Df(3R)p-XT26 85A3;85C1-2 X ray 6, 7 Df(3R)p-XT27 {85A;85A} X ray 7 Df(3R)p-XT103 85A2;85C1-2 X ray 6, 7 Df(3R)p-XT104 {85A;85A} Df(3R)p-XT118 ` 84F1;85B X ray 3, 7 ( 1 = Bender, Turner, and Kaufman, 1987, Dev. Biol. 119: 418-32; 2 = M.M. Green; 3 = Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95; 4 = Kemphues, Raff, Raff, and Kauf- man, 1980, Cell 21: 445-51; 5 = Kemphues, Raff, and Kauf- man, 1983, Genetics 105: 345-56. 6 = Lehmann and Nusslein-Volhard, 1986, Cell 47: 141-52; 7 = Lehmann and Nusslein-Volhard, 1987, Dev. Biol. 119: 402-07; 8 = Tautz, Lehmann, Schnurch, Schuh, Seifert, Kienlin, Jones and Jackle, 1987, Nature (London) 327: 383-89. | DNA coordinates from 85A map (Jones and Rawls, 1988, Genet- ics 120: 733-42) ("+" values to right, "-" values to left or centromere end of map). Proximal breakpoints of defi- ciencies 5, 16, and 19; distal breakpoint of deficiency 25. / Distal breakpoint of Df(3R)p13 molecularly mapped to the DNA (Tautz et al., 1987). ` Includes Dhod (Porter and Rawls, 1984, Mol. Gen. Genet. 193: 27-32). - Uncovers hb. Deficient for pum (Lehman and Nusslein-Volhard, 1987, Nature 329: 167-70). # Df(3R)P2: Deficiency (3R) Pasadena cytology: Df(3R)89D9-E1;89E2-3. origin: X ray induced. discoverer: E.B. Lewis. references: 1980, DIS 55: 207-08. genetics: Deficient for abx-iab3. Genetically similar to Df(3R)Ubx109. molecular biology: Right breakpoint 75-81 kb to the right of the right breakpoint of In(3R)Cbxrv1 (Karch, Weiffenbach, Peifer, Bender, Duncan, Celniker, Crosby, and Lewis, 1985, Cell 43: 81-96). # Df(3R)P9 cytology: Df(3R)89D9-E1;89E4-5. origin: X ray induced. discoverer: E.B. Lewis. references: 1978, Nature 276: 565-70. 1980, DIS 55: 207-08. Jimenez and Campos-Ortega, 1981, Wilhelm Roux's Arch. Dev. Biol. 190: 370-73. Morata, 1982, Am. Zool. 22: 57-64. Levine, Hafen, Garber, and Gehring, 1983, EMBO J. 2: 2037-46. Hafen, Levine, and Gehring, 1984, Nature 307: 287-89. genetics: Deficient for entire BXC; uncovers tuh-3 (Kuhn, Woods, and Andrew, 1984, DIS 60: 134-35). Homozygotes die in late embryonic or early larval stages, showing transformation of metathorax and anterior first abdominal segment to mesothorax (Lewis, 1978; Hayes, Sato, and Denell, 1984, Proc. Nat. Acad. Sci. USA 81: 545-49) and transformation of poste- rior meso- and metathorax to prothorax (Hayes et al., 1984; Ganger, Fehon, and Schubiger, 1985, Nature 313: 395-97). When incubated at 18, homozygous Df(3R)P9 embryos do not com- plete germ band shortening but Df(3R)P9/Dp(3;3)P5 heterozy- gotes go through normal development (Ganger and Schubiger, 1984, DIS 60: 108-09). Df(3R)P9/+ flies show reduced male pigmentation on AB5 and AB6, are sterile, and have deformed genitalia; Df(3R)P9/Mcp flies are partially fertile. Df(3R)P9/Df(3R)Ubx109 larvae have a short tracheal trunk between AB7 and AB8 and a posterior spiracle in AB8 (Lewis, 1978). molecular biology: Right breakpoint 225-230 kb to the right of the right breakpoint of In(3R)Cbxrv1 (Karch, Weiffenbach, Peifer, Bender, Duncan, Celniker, Crosby, and Lewis, 1985, Cell 43: 81-96). # Df(3R)P10: see Tp(3;2)P10 # Df(3R)P-10 - Df(3R)P-79 origin: X ray induced loss of TE87A. references: Reuter, Gausz, Gyurkovics, Friede, Bang, Spierer, Hall, and Spierer, 1987, Mol. Gen. Genet. 210: 429-36. genetics: Suppress wm4h variegation. deficiency cytology ______________________________ Df(3R)P-10 86E6-9;87A9-B1 Df(3R)P-21 86E19-F1;87B11-15 Df(3R)P-29 87A4-5;87B4-5 Df(3R)P-35 86F3-4;87B5-8 Df(3R)P-79 86E1-2;87B1-2 # Df(3R)P13 cytology: Df(3R)89C-D;89E. origin: X ray induced. discoverer: Ramey. references: Karch, Weiffenbach, Peifer, Bender, Duncan, Cel- niker, Crosby, and Lewis, 1985, Cell 43: 81-96. molecular biology: Right breakpoint 78-81 kb to the right of the right breakpoint of In(3R)Cbxrv1. # Df(3R)P14 cytology: Df(3R)90C2-D1;91A2-3. origin: X ray induced. discoverer: E. B. Lewis. references: Grell, 1976, Genetics 83: s28-29. Detwiler and MacIntyre, 1978, Biochem. Genet. 16: 1113-32. genetics: Deficient for DNase-1, sr, and gl but not k or Dl. # Df(3R)P47: see Tp(3;3)P47 # Df(3R)P88: see Df(3R)ss # Df(3R)P115: see Tp(3;1)P115 # Df(3R)Pc-T7: Deficiency (3R) Polycomb origin: / ray induced. discoverer: Tiong. references: Kennison and Russell, 1987, Genetics 116: 75-86. genetics: Deficient for Pc. # Df(3R)Po: Deficiency (3R) Pyridoxal oxidase references: Hughes, Nelson, Yanuk, and Szauter. genetics: Deficient for Po (Hughes et al.) and mor (Kennison). deficiency cytology _______________________________ Df(3R)Po3 89A1-2;89A11-13 Df(3R)Po4 88F7-89A1;89A11-13 # Df(3R)Pr: Deficiency (3R) Prickly origin: X ray induced. discoverer: Preiss. references: Preiss, Hartley, and Artavanis-Tsakonas, 1988, EMBO J. 7: 3917-27. deficiency cytology synonym _____________________________________ Df(3R)Pr1 96F11-14;97E2-3 Prrev1 Df(3R)Pr4 96F11-14?;97B Prrev4 Df(3R)Pr6 96F11-14;98A Prrev6 Df(3R)Pr10 96F11-14;97C1 Prrev10 Df(3R)Pr-P9 96F11-14;97D8-10 PrP9 # Df(3R)r1-G6 cytology: Df(3R)93A2-B1;93E-F. references: Vincent. genetics: Deficient for the gene encoding (Na+K+) (ATPase, (Atp. # Df(3R)R29 references: Whetten, Organ, Krasney, Cox-Foster, and Cavener, 1988, Genetics 120: 475-84. genetics: Df(3R)A41/Df(3R)R29 flies lack GLD enzyme activity. # Df(3R)red: Deficiency (3R) red Malpighian tubules genetics: Df(3R)red/+ progeny of Df(1)C128/+ females show a high frequency of homeotic transformations (Gans et al., 1980). deficiency cytology ref ( genetics _____________________________________________________________ Df(3R)red1 88B1;88D3-4 2, 4 trx-- red- Df(3R)red2l 88A12-B1;88B2-3 1, 9 trx-- red- Df(3R)red3l 87F12-14;88C1-3 1, 2, 3, 8 Dip-B-- red- Df(3R)red-P1 88B1;88D3-4 2 trx-- red- Df(3R)red-P6 88B1;88D3-4 2 trx-- red- Df(3R)red-P52 88A12-B1;88B4-5 1, 5, 6, 7 trx-- su(Hw)- Df(3R)red-P93 88B-C (Lewis) 2, 5, 7 trx-- red- ( 1 = Capdevila and Garcia-Bellido, 1981, Wilhelm Roux's Arch. Dev. Biol. 190: 339-50 2 = Gans, Forquignon, and Masson, 1980, Genetics 96: 887-902; 3 = Hall and Kankel, 1976, Genetics 83: 517-35; 4 = Ingham, 1980, DIS 55: 63-64; 5 = Ingham, 1981, Wilhelm Roux's Arch. Dev. Biol. 190: 339-50; 6 = Ingham and Whittle, 1980, Mol. Gen. Genet. 179: 607-14; 7 = Lewis, 1981, Developmental Biology Using Purified Genes (Brown and Fox, eds.). Academic Press, New York, pp. 189-208; 8 = Ohnishi and Voelker, 1981, Biochem. Genet. 19: 75-85; 9 = Spillman and Nothiger, 1978, DIS 53: 163. # Df(3R)rn: Deficiency (3R) rotund references: Agnel, Kerridge, Vola, and Griffin-Shea, 1989, Genes Dev. 3: 85-95. genetics: Deficient for rn. deficiency cytology origin discoverer ____________________________________________________ Df(3R)rn3 84D3;84D4 X ray Hannah-Alava Df(3R)rn5 84D3;84D4 X ray Williams Df(3R)rn17 ( 84B-C;84D9-12 DEB Kerridge Df(3R)rn19 84D3;84D4 DEB Kerridge Df(3R)rn20 ( 84D3;84D4 DEB Kerridge Df(3R)rn22 ( 84B-C;84D9-10 DEB Kerridge ( Deficiency includes roe. # Df(3R)ry: Deficiency (3R) rosy origin: X ray induced. deficiency cytology ref ( genetics molecular coordinates of breakpoint | ___________________________________________________________________________________________________________________________ Df(3R)ry1 87D;87E-F 1 kar-- ry- Df(3R)ry27 87D1-2;87F1-2 2, 6, 7, 8 l(3)87Da-- l(3)87Ek- *Df(3R)ry28 7, 8 ry- *Df(3R)ry29 7, 8 ry- *Df(3R)ry30 7, 8 ry- *Df(3R)ry31 7, 8 ry- *Df(3R)ry32 7, 8 ry- *Df(3R)ry33 7, 8 ry- *Df(3R)ry34 7, 8 ry- Df(3R)ry36 87E;87E 4, 7, 8, 9 mesA-- ry-; also snk- proximal -201 to -213; *Df(3R)ry51 7, 8 ry- Df(3R)ry52 7, 8 kar-- l(3)87Eb- *Df(3R)ry66 7, 8 ry- *Df(3R)ry70 7, 8 ry- Df(3R)ry74 87D8;87D12 6 ry- Df(3R)ry75 87D1-2;87D14-E1 4, 6, 9 l(3)87Da-- pic- distal -125 to -139 Df(3R)ry76 87D13-E1;88B12-14 6 ry- *Df(3R)ry77 / l(3)87Da-- pic- *Df(3R)ry78 / mes-- Ace- Df(3R)ry81 87C1-3;87D14-E2 2,3,4,9,10 l(3)87Ca-- pic-; includes Men distal -100 to -112 Df(3R)ry85 87B15-C1;87F15-88A1 2, 10 l(3)87Ca-- l(3)87Ek-; includes Men Df(3R)ry614 87D2-4;87D11-14 2,3,4,9 l(3)87Ca-- pic- distal -125 to -139 Df(3R)ry615 ` 87B12-15;87E8-11 2, 10 l(3)87Ca-- l(3)87Ej-; includes Men Df(3R)ry619 87D7-9;87E12-F1 2, 3, 4, 9 mesA-- l(3)87Ek- proximal -201 to -213 Df(3R)ry1168 87B15-C1;87E9-12 3, 4 l(3)87Ca-- l(3)87Ej- Df(3R)ry1301 87D2-4;87E1-2 3, 4, 9 l(3)87Da-- l(3)87Ec- distal +15 to +21.5 - Df(3R)ry1402 87D2-4;87D14-E2 2, 3, 4, 9 l(3)87Da-- l(3)87Eb- distal -39 to -60 Df(3R)ry1607 87D3-4;87E2-3 3, 4, 9 l(3)87Da-- Ace- distal +26 to +32 - Df(3R)ry1608 87D4-6;87E1-2 3, 4, 9 l(3)87Dd-- l(3)87Eb- distal -17 to -41 Df(3R)ry-K 87B;87E (Richmond) 5, 8 l(3)S1 Ace- ( 1 = Grell, E.H., 1962, Z. Indukt. Abstamm. Vererbungsl. 93: 371-77; 2 = Hall and Kankel, 1976, Genetics 83: 517- 35; 3 = Hilliker, Chovnick, and Clark, 1981, DIS 56: 64-72; 4 = Hilliker, Clark, Chovnick, and Gelbart, 1980, Genetics 95: 95-110; 5 = Kernaghan, 1964, DIS 39: 62-64; 6 = Lefevre, 1971, DIS 46: 40; 7 = Schalet, 1964, DIS 39: 62-64; 8 = Schalet, Kernaghan, and Chovnick, 1964, Genetics 50: 1261-68; 9 = Spierer, Spierer, Bender, and Hogness, 1983, J. Mol. Biol. 168: 35-50; 10 = Voelker, Ohnishi, Langley, Gausz, and Gyurkovics, 1981, Biochem. Genet. 19: 525-34. | Coordinates of either proximal or distal breakpoints given with respect to arbitrarily-chosen 0 (Spierer et al., 1983), "+" values to right, "-" values to left. / Described in CP627. ` Also see Garcia-Bellido, Moscoso del Prado, and Botas, 1983, Mol. Gen. Genet. 192: 253-63. - Gausz, Hall, Spierer, and Spierer, 1986, Genetics 112: 65- 78; Hall and Spierer, 1986, EMBO J. 5: 2949-54. # Df(3R)ro: Deficiency (3R) rough deficiency cytology discoverer ref ( genetics ____________________________________________________________________ Df(3R)ro80b 97D1;97D15 Peter Lewis 1,2 Tl-, ro- Df(3R)ro82b 96F11-14;97F3-11 3 ro- Df(3R)ro-XB3 97D1-2;97D9 Peter Lewis 1,4 Tl-, ro-; 40% viable over Tlrv Df(3R)ro-z1 97D1-2;97D15 Peter Lewis 4 ro- ( 1 = Anderson, Jurgens, and Nusslein-Volhard, 1985, Cell 42: 779-89; 2 = Anderson, Bokla, and Nusslein-Volhard, 1985, Cell 42: 791-98; 3 = Preiss, Hartley, and Artavanis- Tsakonas, 1988, EMBO J. 7: 3917-27; 4 = Tomlinson, Kimmel, and Rubin, 1988, Cell 55: 771-84. # Df(3R)roe: Deficiency (3R) roughened eye cytology: 84A6-B1;84D4-9. discoverer: Jurgens. references: Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95. genetics: Deficient for Scr, ftz, and Antp. # Df(3R)ry: Deficiency (3R) rosy origin: X ray induced. (Other information in table at top of page). # Df(3R)ry+: see Tp(3;2)ry+ # Df(3R)S462: Deficiency (3R) of Shaw cytology: Df(3R)89D1-2;90D1. origin: Aneuploid recombinant from Tp(3;3)S462/+. discoverer: Shaw, 1973. references: Lewis, 1980, DIS 55: 207-08. genetics: Df(3R)S462/+ viable but ecloses one or two days later than wild type. # In(3R)sbd: Inversion (3R) stubbloid origin: X ray induced. references: Spillman and Nothiger, 1978, DIS 53: 164-65. genetics: Homozygous lethal in first larval instar. inversion cytology _____________________________ In(3R)sbd12 88B2-C1;89B3-16 In(3R)sbd17 81;89B10-12 In(3R)sbd21 86D2-E1;89B3-12 # Df(3R)SCB-XL2 cytology: Df(3R)84A4-5;84B1-2. origin: X ray induced. discoverer: Jurgens. references: Pultz, Diederich, Cribbs, and Kaufman, 1988, Genes Dev. 2: 901-20. genetics: Variegating for pb. Df(3R)SCB-XL2/pb- flies show the maxillary and labial palp phenotypes of pb null flies. # Df(3R)Scr: Deficiency (3R) Sex combs reduced cytology: Df(3R)84A1-2;84B1-2. origin: / ray induced. discoverer: Sinclair, 1977. references: Kaufman, Lewis, and Wakimoto, 1980, Genetics 94: 115-33. Lewis, Kaufman, and Denell, 1980, DIS 55: 85-87. Lewis, Kaufman, Denell, and Tallerico, 1980, Genetics 95: 367-81. Lewis, Wakimoto, Denell, and Kaufman, 1980, Genetics 95: 383-97. Wakimoto, Lewis, and Kaufman, 1980, DIS 55: 140-41. Wakimoto and Kaufman, 1981, Dev. Biol. 81: 51-64. Garber, Kuroiwa, and Gehring, 1983, EMBO J. 2: 2027-36. genetics: Deficient for pb-Hu plus four lethal complementation groups proximal to pb. Associated with dominant reduced-sex- comb phenotype. Fails to complement the recessive lethalities of Msc, Antp, and AntpScx. Embryonic lethal with Df(3R)Antp17. molecular biology: Deletes sequences to left of molecular coor- dinate +100, In(3R)Hu breakpoint being coordinate 0 in the breakpoint DNA walk of Garber et al., 1983 ("+" values to the left, "-" values to the right). # Df(3R)Scx2: Deficiency (3R) Sexcombs extra cytology: Df(3R)84A4-5;84C1-2. Break near C1, probably C2 or C3 (B. Baker). origin: X ray induced. synonym: Df(3R)ScxW+RX2; Df(3R)Antp-Scx. references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. Cavener, Corbett, Cox, and Whetten, 1986, EMBO J. 5: 2939-48. Pultz, Diederich, Cribbs, and Kaufman, 1988, Genes Dev. 2: 901-20. genetics: Deficient for pb, ftz, ScxW and Antp. Homozygous lethal. Df(3R)Scx2/Df(3R)MAP2 viable and pb. molecular biology: Distal (84C1-2) breakpoint located at about +41 kb (Baker and Wolfner, 1988, Genes Dev. 2: 477-89); 0 point = HindIII site in (Tub84B, "+" values to the right, "-" values to the left). # Df(3R)Scx4 cytology: Df(3R)84B3;84D1-2. origin: X ray induced. synonym: Df(3R)ScxW+RX4. references: Hazelrigg and Kaufman, 1983, Genetics 105: 581- 600. Cavener, Otteson and Kaufman, 1986, Genetics 114: 111-23. Agnel, Kerridge, Vola, and Griffin-Shea, 1989, Genes Dev. 3: 85-95. genetics: Deficient for ScxW, Antp, rn, and roe but not ftz. Homozygous lethal. # Df(3R)SMG39: Deficiency (3R) Semenova Mglinetz Glotoff cytology: Df(3R)90C;91D. origin: / ray induced. references: Semenova, Mglinetz, and Glotoff, 1970, Genetika (Moscow) 6: 165-69. #*Df(3R)sr: Deficiency (3R) stripe origin: X ray induced. discoverer: Alexander. references: Ward and Alexander, 1957, Genetics 42: 42-54. genetics: Deficient for sr. deficiency cytology ________________________________ *Df(3R)sr100.394 90C2-7;90F3-7 *Df(3R)sr300.24 90C2-4;91A2-5 *Df(3R)sr300.101 90D2-4;91A6-8 # Df(3R)ss: Deficiency (3R) spineless cytology: Deficient for bands in 89C-D; associated with In(3LR)P88=In(3LR)61A;89C-D. origin: X ray induced. discoverer: E.B. Lewis. synonym: Df(3R)P88. references: Garcia-Bellido, Moscoso del Prado, and Botas, 1983, Mol. Gen. Genet. 192: 253-63. genetics: Deficient for ss. # Df(3R)ss-a cytology: Df(3R)89B;89D (Holmgren). origin: Induced by ethyl methanesulfonate. synonym: ssaC15. references: Struhl, 1982, Genetics 102: 737-49. genetics: Deficient for ss. Lethal over Df(3R)bxd100. # Df(3R)su(Hw)7: Deficiency (3R) Suppressor of Hairy wing cytology: Df(3R)88A9;88B2. genetics: Deficient for su(Hw)7. # Df(3R)Su9-b: Deficiency (3R) Suppressor cytology: Df(3R)95A;97A. origin: Spontaneous. references: Gonzales, Molina, Casal, and Ripoll, 1989, Genetics 123: 371-77. genetics: Deficient for M(3)96A-Pr. Dominant lethal. # Df(3R)Su(var)3-6: Deficiency (3R) Suppressor of variegation cytology: Df(3R)87B1;87D11. origin: X ray induced. references: Reuter, Dorn, Wustmann, Friede, and Rauh, 1986, Mol. Gen. Genet. 202: 481-87. Reuter, Gausz, Gyurkovics, Friede, Bang, Spierer, Hall, and Spierer, 1987, Mol. Gen. Genet. 210: 429-36. genetics: Deficient for Su(var)3-6. Recessive lethal. # Df(3R)SX1 cytology: Df(3R)89E;89E. origin: X ray induced. references: Tiong, Bone, and Whittle, 1985, Mol. Gen. Genet. 200: 335-42. Karch, Weiffenbach, Peifer, Bender, Duncan, Celniker, Crosby, and Lewis, 1985, Cell 43: 81-96. genetics: Deficient for iab2 - iab9. molecular biology: Proximal breakpoint 27.5-35 kb to the right of the right breakpoint of In(3R)Cbxrv1 (Karch et al., 1985). # Df(3R)T origin: Derived from transposing element TE86F. deficiency cytology ref ( genetics ____________________________________________________________ Df(3R)T-7 86F1-2;86F4-7 2 l(3)86Fa-- l(3)86Fb- Df(3R)T-10 | 86F1-2;87C6-7 1, 2 l(3)87Ca-- l(3)87Cb- Df(3R)T-32 | 86E2-4;87C6-7 1, 2 l(3)87Ca-- l(3)87Cb- Df(3R)T-41 86F1-2;87C1-2 2, 4 lacks 87A7 and 87C1 heat shock puff sites Df(3R)T-45 | 86E;87B5-6 2, 5 l(3)86Fa-- l(2)86Fb; lacks 87A7 heat shock puff site Df(3R)T-47 86F1-2;87A9 2, 5 l(3)86Fa-- l(3)87Ac-; lacks 87A7 heat shock puff site; mgr- Df(3R)T-55 / 86F1-2;87A6-7 2, 3 l(3)86Fa-- l(3)87Ab- Df(3R)T-61 86F1-2;87A9 2 lacks 87A7 heat shock puff site; mgr- Df(3R)T-63 86F1-2;87A5-7 2, 6 sad- ( 1 = Gausz, Bencze, Gyurkovics, Ashburner, Ish-Horowicz, and Holden, 1979, Genetics 98: 917-34; 2 = Gausz, Gyurkovics, Bencze, Awad, Holden, and Ish-Horowicz, 1981, Genetics 98: 775-89; 3 = Goldberg, Paro, and Gehring, 1982, EMBO J. 1: 93-98; 4 = Ish-Horowicz and Pinchin, 1980, J. Mol. Biol. 142: 231-45; 5 = Jurgens, Wieschaus, Nusslein-Volhard, and Kluding, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 283-95; 6 = Ohnishi and Voelker, 1981, Biochem. Genet. 19: 75-85. | Suppresses wm4h variegation (Reuter, Gausz, Gyurkovics, Friede, Bang, Spierer, Hall, and Spierer, 1987, Mol. Gen. Genet. 210: 429-36). / Isolated as pale apricot variant from stock carrying TE86F (Ish-Horowicz). Deletion breakpoint 9 kb to left of Hsp70. # In(3R)Tlrv: Inversion (3R) Toll-revertant references: Anderson, Jurgens, and Nusslein-Volhard, 1985, Cell 42: 779-89. genetics: Revertants of Tl. Homozygous lethal. Heterozygous females viable, fertile, and produce dorsalized embryos as maternal effect. inversion cytology origin synonym _____________________________________________________ In(3R)Tlrv5 97D;98F X ray In(3R)TlRXJ In(3R)Tlrv6 97D;99E-F X ray In(3R)TlRXZ In(3R)Tlrv12 97D;98B EMS In(3R)Tl5BREN In(3R)Tlrv17 97A;97B;97D ( EMS In(3R)Tl5BREN In(3R)Tlrv19 97D;98C-D EMS In(3R)Tl9QRE ( Deficient for 97A-B. #*Df(3R)tll: Deficiency (3R) tailless origin: X ray induced. deficiency cytology ref ( genetics ______________________________________________________ Df(3R)tll-e / 100A1-2;100B5-9 1, 3-5 tll-- Chp- Df(3R)tll-f 100A2-3;100C1-2 4 tll-- Chp- Df(3R)tll-g ?;100B3-4 1, 4, 5 tll- Df(3R)tll-pgx 100A1-2;100B1-2 2 tll- ( 1 = Mahoney and Lengyel, 1987, Dev. Biol. 122: 464-70; 2 = Pignoni, Baldarelli, Steingrimsson, Diaz, Patapoulian, Merriam, and Lengyel, 1990, Cell 62: 151-63; 3 = Strecker, Kongsuwan, Lengyel, and Merriam, 1986, Dev. Biol. 113: 64- 76; 4 = Strecker, Merriam, and Lengyel, 1988, Development 102: 721-34; 5 = Van Vactor, Krantz, Reinke, and Zipursky, 1988, Cell 52: 281-90. / Molecular biology: Homozygous deficiency embryos show six instead of seven ftz protein stripes (Mahoney and Lengyel, 1987). # Df(3R)Tpl: Deficiency (3R) Triplo-lethal genetics: Deficient for Tpl region at 83D-E. Viable over Tpl duplications, but lethal over wild-type 3's or Tpl deficien- cies. other information: Two more putative deficiencies (synonyms: 20c76 and 25e76) were viable over wild-type 3's, but the stocks were lost because of male sterility and not tested further. deficiency cytology origin ( ref | synonym ________________________________________________________________________ Df(3R)Tpl1 83D4-5;83E1-2 synthetic, / ray 1, 2 Df(3R)3g74 Df(3R)Tpl2 83D4-5;84A1-2 X ray 1, 2 Df(3R)1c77 Df(3R)Tpl3 83D4-5;84A4-5 EMS 1, 2 Df(3R)5f77 Df(3R)Tpl4 83D4-5;83E1-2 EMS 1, 2 Df(3R)10d77-7 Df(3R)Tpl5 83D1-2;83E1-2 EMS 1, 2 Df(3R)25g77 Df(3R)Tpl6 83D1-2;84A4-5 / ray 1, 2 Df(3R)26b77 Df(3R)Tpl7 83D4-5;83E1-2 / ray 1, 2 Df(3R)28b77 Df(3R)Tpl8 83D4-5;83E1-2 EMS 1, 2 Df(3R)28f77 Df(3R)Tpl9 83D4-5;84A4-5 / ray 1, 2 Df(3R)29c76 Df(3R)Tpl10 83C1-2;84B1-2 / ray 1, 2 Df(3R)30c76 Df(3R)Tpl11 / lacks 83E EMS 3 tpl16 Df(3R)Tpl12 / lacks 83E EMS 3 tpl25 Df(3R)Tpl13 / lacks 83E EMS 3 tpl36 Df(3R)Tpl14 / lacks 83E EMS 3 tpl37 ( Df(3R)Tpl1 was induced in Df(3R)Tpl/Dp(3;3)Tpl females, while the other deficiencies were induced in wild-type males (Keppy and Denell, 1979). | 1 = Denell and Keppy, 1979, Genetics 93: 117-30; 2 = Keppy and Denell, 1979, Genetics 91: 421-41; 3 = Roehrdanz and Lucchesi, 1980, Genetics 95: 355-66. / Also deficient for Ki. Salivaries lack quinacrine-bright region at 83D-E. # Df(3R)trxE8: Deficiency (3R) trithorax origin: EMS induced. discoverer: Kennison. genetics: red+trx-su(Hw)-cv-c+. # Df(3R)trxE12 origin: EMS induced. discoverer: Kennison. genetics: red-trx-su(Hw)-cv-c+. # In(3R)Ubx: Inversion (3R) Ultrabithorax genetics: Associated with Ubx alleles. discov inversion cytology origin synonym or ref ( ___________________________________________________________________ In(3R)Ubx6Q 89E3-4;96F;97A Ubx21560.6Q 7 In(3R)Ubx7L 89E1-2;96A X ray Ubx19286.7L In(3R)Ubx16N 89E;99 X ray Ubx19286.16N 7 In(3R)Ubx30A 89E1-2;91B X ray Ubx3966.30 In(3R)Ubx80 87F-88A;89E EMS Ubx16800.752 1 In(3R)Ubx125 81;89E X ray 5 In(3R)Ubx961 89E;96 In(3R)UbxG2 89E;96A1-7 X ray Ubx19286 5 In(3R)UbxK 89E;92A X ray Cbx+R1 3 In(3R)UbxKM5 | 88B;89E1-2 X ray Ubx12.5 4 In(3R)UbxKM22 | 88F;89E1-2 X ray Ubx5.22 4 In(3R)UbxP18 81F;91F-92 5 In(3R)UbxR5 89E;92A X ray CbxrvR17.5E 6 In(3R)UbxR6 87;89E X ray CbxrvR17.6F 6 In(3R)UbxR14 87D-E;89E X ray CbxrvR17.14P 2, 6 In(3R)UbxR20 87B-D;89E X ray CbxrvR17.20V 2, 6 In(3R)UbxX 89E;98B-C X ray 5 ( 1 = Bacher, 66h; 2 = Bender, Spierer, and Hogness, 1983, J. Mol. Biol. 168: 17-33; 3 = Kaufman; 4 = Kerridge and Morata, 1982, J. Embryol. Exp. Morphol. 68: 211-34; 5 = Lewis; 6 = Ramey; 7 = Smit, 72i. | Homozygotes lethal; heterozygotes weak Ubx. # Df(3R)urd: Deficiency (3R) urdur cytology: Lacks several bands in 87F. origin: / ray induced. discoverer: Kennison, 1983. synonym: Df(3R)JK6;urd1. references: Kennison and Tamkun, 1988, Proc. Nat. Acad. Sci. USA 85: 8136-8140. genetics: Viable in combination with Df(3R)ry27 = Df(3R)87D1- 2;87F1-2 and Df(3R)red-P52 = Df(3R)88A12-B1;88B4-5. Lethal in combination with Df(3R)l26c = Df(3R)87D14-E1;87F11-12 and with Df(3R)red31 = Df(3R)87F12-14;88C1-3. # In(3R)V: Inversion (3R) Valencia origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. inversion cytology genetics __________________________________________ In(3R)V9-8 81-82A;89A-B lethal In(3R)V16 93F;99C + detrimental T(2;3)60B-C;84A In(3R)V103 85A;96E + lethal T(2;3)58F;67B4 # Df(3R)VW4 cytology: Df(3R)85E11;85F11. origin: / ray induced. discoverer: Walker. references: Ashburner, Angel, Detwiler, Faithfull, Gubb, Har- rington, Littlewood, Tsubota, Velissariou, and Walker, 1981, DIS 56: 186-91. genetics: Minute, presumably deficient for M(3)85E. # Df(3R)WIN origin: X ray induced. genetics: Deficient for pb but not lab. Df(3R)WIN/Df(3R)MAP2 viable and pb-. deficiency cytology ref ( _____________________________________ Df(3R)WIN1 84A4-5;84B1-2 3 Df(3R)WIN3 84A4-5;84C1-2 1, 2, 3 Df(3R)WIN11 83E1-2;84A4-5 ( 1 = Cavener, Otteson, and Kaufman, 1986, Genetics 114: 111-23; 2 = Hays, Deuring, Robertson, Prout and Fuller, 1989, Mol. Cell Biol. 9: 875-84; 3 = Pultz, Dieder- ich, Cribbs, and Kaufman, 1988, Genes Dev. 2: 901-20. # Df(3R)X2 cytology: Df(3R)84A4-5;84B1-2. origin: X ray induced. references: Pultz, Diederich, Cribbs, and Kaufman, 1988, Genes Dev. 2: 901-20. genetics: Deficient for pb but not lab. Df(3R)X2/Df(3R)MAP2 viable and pb-. # Df(3R)X3F cytology: Df(3R)99D1-2;99E1. # Df(3R)XS cytology: Df(3R)96A1-7;96A21-25. # Df(3R)XTA1 cytology: Df(3R)95B;95D. discoverer: Jurgens. references: Wustmann, Szidonya, Taubert, and Reuter, 1989, Mol. Gen. Genet. 217: 520-27. # Df(4)3-Df(4)40 origin: X ray induced. deficiency cytology ref ( deficient for ______________________________________________________________ Df(4)3 102E2-10;102F2-10 1-4 l(4)102EFa-sv Df(4)11 102E2-10;102F2-10 1-5 l(4)102EFa-spa Df(4)34 {102E-F} 1 spa Df(4)38 102E2;102E10 2-5 l(4)102EFa-l(4)102EFc Df(4)40 102E2-10;102F1-10 2-5 sv-spa ( 1 = CP627; 2 = Hochman, 1971, Genetics 67: 235-52; 3 = Hochman, 1974, Cold Spring Harbor Symp. Quant. Biol. 38: 581-89; 4 = Hochman, 1976, The Genetics and Biology of Drosophila (Ashburner and Novitski, eds.). Academic Press, London, New York, San Francisco, Vol. 1b, pp. 903-28; 5 = Hochman, Gloor, and Green, 1964, Genetica 35: 109-26. # Df(4)2c: see Df(4)bt-D # Df(4)62e: see Df(4)M101-62e # Df(4)62f: see Df(4)M101-62f # Df(4)63a: see Df(4)M101-63a # Df(4)bt-D: Deficiency (4) bent-Dominant cytology: Df(4)101B6-10. origin: X ray induced. discoverer: Schultz. references: Bridges, 1935, Biol. Zh. (Moscow) 4: 401-20. Hochman, Gloor, and Green, 1964, Genetica (The Hague) 35: 109-26. Hochman, 1971, Genetics 67: 235-52. 1976, The Genetics and Biology of Drosophila (Ashburner and Novitski, eds.). Academic Press, London, New York, San Fran- cisco, Vol. 1b, pp. 903-28. genetics: Deficient for l(4)102CDa-l(4)102CDb. bt phenotype no longer observed (Hochman, 1976). # Df(4)Cat: Deficiency (4) Cataract origin: X ray induced. discoverer: Belgovsky, 1936. references: 1937, DIS 8: 7. Morgan, 1941, DIS 14: 52. Hochman, Gloor, and Green, 1964, Genetica (The Hague) 35: 109-26. Hochman, 1971, Genetics 67: 235-52. genetics: Deficient for l(4)102EFa-sv. # Df(4)ci-D: Deficiency (4) cubitus interruptus-Dominant origin: X ray induced. discoverer: Ruch, 32a18. references: Bridges, 1935, Biol. Zh. (Moscow) 4: 401-20. Hochman, Gloor, and Green, 1964, Genetica (The Hague) 35: 109-26. Hochman, 1971, Genetics 67: 235-52. genetics: Deficient for l(4)102ABb and l(4)102ABc. # Df(4)G: Deficiency (4) of Gloor and Green cytology: Df(4)102E2-10; tip of 4R lost and remainder of chro- mosome 4 capped with X-chromosomal material, including 1A (Hochman). origin: X ray induced. discoverer: Gloor and Green, 1957. references: Hochman, Gloor, and Green, 1964, Genetica 35: 109-26. Hochman, 1971, Genetics 67: 235-52. 1976, The Genetics and Biology of Drosophila (Ashburner and Novitski, eds.). Academic Press, London, New York, San Fran- cisco, Vol. 1b, pp. 903-28. genetics: Deficient for l(4)102EFa-l(4)102EFf; fails to comple- ment sv and spa. Lethal homozygous and in heterozygous combi- nation with Df(4)3, Df(4)11, Df(4)12, Df(4)24, and Df(4)34. y+ and ac+ linked terminally. # Df(4)M: see Df(4)M101 # Df(4)M2: see Df(4)M101-2 # Df(4)M3: see Df(4)M101-3 # Df(4)M4: see Df(4)M101-4 # Df(4)M62e: see Df(4)M101-62E # Df(4)M62f: see Df(4)M101-62f # Df(4)M63-a: see Df(4)M101-63a # Df(4)M101: Deficiency (4) Minute deficiency cytology origin synonym ref ( deficient for _____________________________________________________________________________ Df(4)M101 | 101E-F; spont Df(4)M 1, 2, M(4)101 102B6-17 5, 7 -l(4)102ABi *Df(4)M101-2 {102A1-2; X ray Df(4)M2 1 ci-ar 102B2-5} *Df(4)M101-3 {101E-F; X ray Df(4)M3 2, 3 M(4)101-ar 102B2-5} Df(4)M101-4 {101E-F; X ray Df(4)M4 4 M(4)101-Ce 102B2-5} Df(4)M101-62e / 101E; Df(4)M62e 3 ar-ey 102D13-E1 Df(4)M101-62f 101E; / ray Df(4)M62f 3 M(4)101-ar 102B10-17 Df(4)M101-63a ` 101F2-102A1; Df(4)M63a 3, 5, 6 M(4)101-ci, 102A2-5 not ciD. ( 1 = Bridges, 1935, Biol. Zh. 4: 401-20; 2 = Bridges, 1935, Tr. Dinam. Razvit. 10: 469-70; 3 = CP627; 4 = Glass, 1944, DIS 18: 40; 5 = Hochman, 1971, Genetics 67: 235-52; 6 = Hochman, 1976, The Genetics and Biology of Drosophila (Ashburner and Novitski, eds.). Academic Press, London, New York, San Francisco, Vol. 1b, pp. 903-28; 7 = Slyzinski, 1944, J. Hered. 35: 322-24. | Right break to left of 102B9-10 according to Bridges, to right according to Slyzinski. / Recovered by Fahmy from progeny of male injected with Droso- phila DNA. ` Recovered by Fahmy from progeny of male injected with thymus extract from leukemic mice ("Gross Factor"). Eclosion delayed. # Df(w-ec)64d: see Tp(1;2)w-ec