DEFICIENCIES # Del(1): see Dp(1;f) # Del(Xc2): see Dp(1;f)R # Df-3LK: see Df(3L)K # Df(1)0-sc,LVM: see Df(1)260-1 # Df(1)05-22-1 references: Fleming. genetics: Deficient for l(1)1Aa through l(1)1Ad. # Df(1)1-96 references: Fleming, DeSimone, and White, 1989, Mol. Cell Biol. 9: 719-25. genetics: Deficient for l(1)1Aa through ewg. # Df(1)1D1 cytology: Df(1)14D;15C. references: Mason, Green, Shaw, and Boyd, 1981, Mutat. Res. 81: 329-43. genetics: Deficient for M(1)14F. # Df(1)2/9A cytology: Df(1)20B;20C. origin: Induced by MR. references: Eeken, Sobels, Hyland, and Schalet, 1985, Mutat. Res. 150: 261-75. genetics: Deficient for l(1)20Bb1. # Df(1)2/19B cytology: Df(1)19F. origin: Induced by MR. references: Eeken, Sobels, Hyland, and Schalet, 1985, Mutat. Res. 150: 261-75. genetics: Deficient for fliI-l(1)19Fg2. # Df(1)2F1-3A4 cytology: Df(1)2F1;3A4. discoverer: Green. references: Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. 1985, Genetics 111: 23-41. genetics: Deficient for l(1)2Fb-gt. molecular biology: Breakpoint mapped to the DNA at +73.5 (Xho site) and +75.0 (Hind III site) by Haenlin, Steller, Pirrotta, and Mohier, 1985, Cell 40: 827-37. # Df(1)5-13 genetics: Deficient for l(1)1Aa through l(1)1Ac. #*Df(1)7aA: Deficiency (1) 7a from Austin cytology: Df(1)3C3-5;3C7-9; inferred from Mackensen's fig. 15F (1935). origin: X ray induced. references: Mackensen, 1935, J. Heredity 26: 163-74 (fig.). genetics: Deficient for fa and spl but not w or ec; heterozy- gous female N. # Df(1)10-70d cytology: Df(1)8D3;8D8-9. origin: Induced by mutator gene mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. genetics: Deficient for lz. # Df(1)10RA cytology: 8-13 band deficiency including 7A. discoverer: Cline. references: Nicklas and Cline, 1980, Genetics 94: s76. genetics: Deficient for Sxl but not cm or ct. # Df(1)11-83 cytology: Df(1)2F2;3A6. discoverer: Schalet. # Df(1)12-70b cytology: Xh26-Xh33. origin: Induced by mutator gene mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. # Df(1)13-70b cytology: Df(1)1A7;1B4. origin: Induced by mutator gene mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. # Df(1)13C3 cytology: Df(1)20A3;20E-F. origin: X ray induced. references: Schalet and Lefevre, 1973, Chromosoma 44: 183-200. genetics: Deficient for wap to su(f). #*Df(1)14zA origin: X ray induced. discoverer: Mackensen. references: 1935, J. Heredity 26: 163-74 (fig.). genetics: Deficient for f but not fw or r. # Df(1)16-, Df(1)17-, Df(1)18- cytology: A series of deficiencies for the proximal-most X- linked genes; breakpoints tabulated below. origin: Neutron induced. discoverer: Munoz. references: Schalet, 1972, DIS 49: 36-37. Schalet and Lefevre, 1973, Chromosoma 44: 183-200. 1976, The Genetics and Biology of Drosophila (Ashburner and Novitski, eds.). Academic Press, London, New York, San Fran- cisco, Vol. 1b, pp. 847-902. Yamamoto and Miklos, 1987, DIS 66: 154-55. Perrimon, Smouse, and Miklos, 1989, Genetics 121: 313-31. deficiency cytology genetics ____________________________________________________________ Df(1)16-2-13 {20A1-2;20A4} wap--uncl- Df(1)16-2-19 19A5;19D3 ot--mal- Df(1)16-3-22 19D1;20A2 mal--eo- Df(1)16-3-35 ( 19D2-3;19E3-4 mal--shakB- Df(1)16-3-112 20E;20F su(f)pb--su(f)- Df(1)16-3-162 20E;20F su(f)pb--su(f)- Df(1)16-129 19F1;19F3 lfl--fliI- Df(1)16-185 20E;20F su(f)pb--su(f)- Df(1)17-8 l(1)1Aa--l(1)1Ac- Df(1)17-59 19F5;20E-F l(1)19Fg--su(f)- Df(1)17-87 | 20D-E;20F sph+ su(f)--bb- Df(1)17-137 / 20A;20E-F eo--su(f)- Df(1)17-148 20B-C;20E-F l(1)20Cb--su(f)- Df(1)17-252 20B;20C fog--l(1)20Ca- Df(1)17-257 19F3;20A1-2 fliI--eo- Df(1)17-351 19E;19F l(1)19Ec8--l(1)19Fg2- Df(1)17-408 20A;20F uncl--su(f)- Df(1)17-439 20A;20B wap--stn- Df(1)17-466 20A;20B wap--fog- Df(1)17-489 ` {19E4-5;20E} l(1)19Ed--su(f)- Df(1)18-80 {19F3;19F4} fliI--l(1)19Fe- ( Proximal breakpoint located by Yamamoto and Miklos (1987) between 19E3 and 19E4 instead of 19E6 and 19E7 (Schalet and Lefevre, 1976). The corrected breakpoint is consistant with the viability of Df(1)16-3-35 when heterozygous with Df(1)A118 = Df(1)19E4-5;19E8. | Also see Rahman and Lindsley, 1981, Genetics 99: 49-64. / Df(1)17-137/bbl-158 females are phenotypically bb and more than 50% of them show eo. ` See Baird, Shalet, and Wyman, 1990, Genetics 126: 1045-59. # Df(1)17-8 references: Fleming. genetics: Deficient for l(1)1Aa through l(1)1Ac. # Df(1)17-70b: see Df(1)70b17 # Df(1)18-70d: see Df(1)70d18 # Df(1)19 cytology: Df(1)13F;14E. discoverer: Boyd. references: Steller, Fischbach, and Rubin, 1987, Cell 50: 1139-53. genetics: Deficient for disco and adjacent genes (nearly 5% of X euchromatin deleted). #*Df(1)22 cytology: Df(1)20E;20F. origin: X ray induced. synonym: l(1)22. references: Schalet, 1972, DIS 49: 36-37. Schalet and Lefevre, 1973, Chromosoma 44: 183-200. genetics: Deficient for su(f); mutant for sph. # Df(1)23-70b: see Df(1)70b23 # Df(1)23-70d: see Df(1)70d23 # Df(1)24 origin: Induced by hybrid dysgenesis. discoverer: Sobels. references: Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. genetics: Deficient for pn - l(1)2Ea. #*Df(1)24a origin: X ray induced. discoverer: Mackensen. references: 1935, J. Heredity 26: 163-74 (fig.). genetics: Deficient for w but not pn or fa. # Df(1)26B cytology: Df(1)19F;20. origin: Induced by hybrid dysgenesis. references: Zusman, Coulter, and Gergen, 1985, DIS 61: 217-18. Perrimon, Smouse, and Miklos, 1989, Genetics 121: 313-31. genetics: Deficient for l(1)19Ec-eo. Complements shakB but not l(1)19Ec, l(1)19Ed, or lf. # Df(1)30A2 cytology: Df(1)8F;9B. origin: Induced by ethyleneimine. references: Lim and Snyder, 1968, Mutat. Res. 6: 129-37. # Df(1)46-1 origin: Induced by hybrid dysgenesis. references: Zusman, Coulter, and Gergen, 1985, DIS 61: 217-18. genetics: Complements uncl but not fog or stn. # Df(1)48-2 origin: Induced by hybrid dysgenesis. references: Zusman, Coulter, and Gergen, 1985, DIS 61: 217-18. genetics: Complements eo but not fog or l(1)20Cb. # Df(1)50D3 cytology: Df(1)9A3-4;9F12. discoverer: Nash. genetics: ras--l(1)9Fe. # Df(1)54 cytology: Df(1)19E8-F1;20B3-C1 superimposed on In(1)1B3-4;20B- D1L1B2-3;20B-D1R. new order: 1A - 1B3|20D1 - 20C1|19E8 - 1B3|20D1 - 20F. 19F1 - 20B3 missing; 1B3 duplicated. origin: X ray induced in In(1)scS1Lsc8R. references: Schalet and Lefevre, 1976, The Genetics and Biology of Drosophila (Ashburner and Novitski, eds.). Academic Press, London, New York, San Francisco, Vol. 1b, pp. 846-902. Craymer and Roy, 1980, DIS 55: 200-04. genetics: Deficient for lfl-l(1)20Bb and duplicated for sc. # Df(1)59: see Df(1)ras59 #*Df(1)60b origin: X ray induced. discoverer: Mackensen. references: 1935, J. Heredity 26: 163-74 (fig.). genetics: Deficient for f but not fw or r. # Df(1)62d18 cytology: Df(1)3B1-2;3C6-7. origin: X ray induced. discoverer: Judd, 62d18. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. genetics: Deficient for l(1)3Bb-rst but not N. molecular biology: Left breakpoint localized to an approxi- mately 4 kilobase restriction fragment fifty kilobases to the left of the origin of a 160 kb walk (Gunaratne, Mansukhani, Lipari, Liou, Martindale, and Goldberg, 1986, Proc. Nat. Acad. Sci. USA 83: 701-05). # Df(1)62g18 cytology: Df(1)3A1-2;3A4-5. origin: X ray induced. discoverer: Judd, 62g18. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82. Honisch and Campos-Ortega, 1982, DIS 58: 76-77. genetics: Deficient for gt - l(1)3Ac but not l(1)3Ad. Embryos hemizygous for the deficiency show defects of the cuticle, central nervous system, and head due to absence of the gt locus (Honisch and Campos-Ortega, 1982). Germ-line clones lethal (Garcia-Bellido and Robbins, 1983, Genetics 103: 235- 47). # Df(1)64c4 cytology: Df(1)3A3-4;3C2-3. origin: X ray induced. discoverer: Judd, 64c4. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82. genetics: Deficient for all known loci between z and w. Also deficient for w but not for z. Male lethal in embryo. molecular biology: Left breakpoint localized to a 4 kilobase BamH1 restriction fragment near the origin of a 160-kb walk (Gunaratne, Mansukhani, Lipari, Liou, Martindale, and Gold- berg, 1986, Proc. Nat. Acad. Sci. USA 83: 701-05). # Df(1)64c18 cytology: Df(1)2E1-2;3C2. origin: X ray induced. discoverer: Lefevre. references: Craymer and Roy, 1980, DIS 55: 200-04. Gvozdev, Gerasimova, Kovalev, and Ananiev, 1977, DIS 52: 67- 68. Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. 1985, Genetics 111: 23-41. genetics: Deficient for pn - w. # Df(1)64f1 cytology: Df(1)3A9-B1;3B2-3. origin: X ray induced. discoverer: Abrahamson, 64f1. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 365-82. Young and Judd, 1978, Genetics 84: 723-42. genetics: Deficient for l(1)3Ba, per and l(1)3Bb but not l(1)3Ag or l(1)3Bd. Larval lethal (Judd). Cell lethal in cuticle and in germ-line clones. (Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53). molecular biology: Right breakpoint 82-85 kb distal to the wa copia insertion point (Pirrotta, Hadfield, and Pretorius, 1983, EMBO J. 2: 927-34; Reddy, Zehring, Wheeler, Pirrotta, Hadfield, Hall, and Rosbash, 1984, Cell 38: 701-10). # Df(1)64j4 cytology: Df(1)3A8-9;3B1-2. origin: Found in stocks in separable combination with Df(1)w258-45. discoverer: Judd, 64j4. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82. Young and Judd, 1978, Genetics 88: 723-42. genetics: Deficient for l(1)3Ag and l(1)3Ba but not l(1)3Ae or l(1)3Bb. Also removes per (Bargiello and Young, 1984, Proc. Nat. Acad. Sci. USA 81: 2142-46; Bargiello, Jackson, and Young, 1984, Nature 312: 752-54; Reddy, Zehring, Wheeler, Pirrotta, Hadfield, Hall, and Rosbach, 1984, Cell 38: 701- 10). Cell lethal in cuticle (Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53). Germ-line clones lethal (Garcia- Bellido and Robbins, 1983, Genetics 103: 235-47). molecular biology: Right breakpoint between 89 and 98 kb distal to the wa copia insertion point (Pirotta, Hadfield, and Pre- torius, 1983, EMBO J. 2: 927-34). # Df(1)65j26 origin: X ray induced. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 365-82. Garcia-Bellido and Ripoll, 1973, Nature 273: 399-400. genetics: Deficient for gt-l(1)3Ac. Male lethal in embryo but cell viable in cuticle (Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53). # Df(1)70 cytology: A series of four distally located deficiencies; breakpoints tabulated below. origin: Induced by mutator gene mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. deficiency synonym cytology ______________________________________ Df(1)70b17 17-70b 1A1;1B1-2 Df(1)70b23 23-70b 2F6;3C5 Df(1)70d18 18-70d 1E3;2A3 Df(1)70d23 23-70d 1A1;1B1-2 # Df(1)80 - Df(1)82 origin: X ray induced in Dp(1;4)r+. synonym: Df(1)para. references: Falk, Roselli, Curtiss, Halladay, and Klufas, 1984, Mutat. Res. 126: 25-34. genetics: Deficient for para. deficiency cytology genetics ___________________________________________________________________ Df(1)80e3d ( 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)80e19a 14A1-2;15A6-11 l(1)14Ab-l(1)15Ab Df(1)80e27a 14A1-2;15A6-11 l(1)14Ba-l(1)15Ab Df(1)80f3c 14A1-2;14E l(1)14Aa-l(1)14Ea Df(1)80f8b 14A1-2;14F l(1)14Aa-l(1)14Ea Df(1)80f15f 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)80f18c 14C4-5;15A3-4 (Banga and Boyd) para-l(1)15Aa Df(1)80f25a 14A1-2;15A6-11 l(1)14Ba-l(1)15Ab Df(1)80f29d 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)80g12a 14B3-4;15A6-11 l(1)14Ba-l(1)15Ab Df(1)81f12a 14B5-18;15A6-11 para-l(1)15Aa Df(1)81f20a 14B5-18;15A3-4 l(1)14Ba-l(1)15Aa Df(1)81f20e 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)81g1i 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)81h24b 14B5-18;14E l(1)14Ba-para Df(1)81i21c 14B3-4;14C6-8 l(1)14Ba-para Df(1)81i25b 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)81j6c 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)81j6e 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)81j16f 14A1-2;15A6-11 l(1)14Aa-l(1)15Ab Df(1)81j23a 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)81j29i 14B5-18;15A1-2 l(1)14Ba-l(1)14Fa Df(1)81k19b ( 14B5-18;15B l(1)14Ba-l(1)15Ab Df(1)81k21e 14B5-18;15A5 l(1)14Ba-l(1)15Ab Df(1)81k23b 14B5-18;15A3-4 l(1)14Ba-l(1)15Aa Df(1)81l1b | 14B5-18;15A3-4 l(1)14Ba-l(1)15Aa Df(1)81l8g 14C6-8;15A3-4 para-l(1)14Fa Df(1)81l12h 14B5-18;15A6-11 l(1)14Bb-l(1)15Ab Df(1)81l17h 14A1-2;15A1-2 l(1)14Aa-l(1)14Fa Df(1)81l19i 14B5-18;15A1-2 l(1)14Aa-l(1)14Fa Df(1)81l28f 14B5-18;15A6-11 l(1)14Ba-l(1)15Ab Df(1)82a2y 14B5-18;15A3-4 para-l(1)15Aa Df(1)82a2z 14B5-18;15A3-4 l(1)14Ba-l(1)15Aa Df(1)82b6w ( 14B5-18;14E l(1)14Ba-para Df(1)82b10w | 14C6-8;15A3-4 para-l(1)15Aa Df(1)82b26c 14C6-8;15A3-4 para-l(1)15Aa Df(1)82c3k ( 14B3-4;14E l(1)14Ba-para Df(1)82c5b 14B5-18;15A3-4 l(1)14Ba-l(1)15Aa Df(1)82c19i 14A1-2;14D3-4 l(1)14Ba-para Df(1)82c25g 14A1-2;15A3-4 l(1)14Aa-l(1)15Aa? Df(1)82d7e 14B5-18;14D3-4 l(1)14Ba-para ( Deficient for diss (Kulkarni, Steinlauf, and Hall, 1988, Genetics 118: 267-85). | Complex. #*Df(1)172-Df(1)247g origin: X ray induced. references: Patterson, 1932, Am. Naturalist 66: 193-206. deficiency genetics ____________________________ *Df(1)172 pn--ec- *Df(1)231c v- *Df(1)235 pn--ec- *Df(1)244 m- *Df(1)247a m- *Df(1)247g w- # Df(1)203: see Df(1)ras203 # Df(1)208 - Df(1)228 origin: Induced by methyl methanesulfonate. references: Paradi, Vogel, and Szilagyi, 1983, Mutat. Res. 111: 145-59. genetics: Recessive lethal. deficiency cytology _______________________________ Df(1)208 20C-D;F Df(1)216 ( 20A;20A Df(1)217 ( 19D-E;20F Df(1)218 19F;19F Df(1)228 19A-B;19A-B ( Double mutant. # Df(1)217: see Df(1)ras217 #*Df(1)258-44: see T(1;2;3)wm258-44 # Df(1)259 origin: X ray induced in y. synonym: l259, l(1)J1259. references: Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1649-70. genetics: Male lethal with normal Y but viable with y+Y. Defi- cient for l(1)1Aa through l(1)1Ac. # Df(1)260-1 - *Df(1)260-19 origin: Df(1)260-1 is spontaneous; the other deficiencies are X ray induced. deficiency cytology ref ( genetics __________________________________________________________ Df(1)260-1 | 1A1;1B4-6 1, 2, 3, 5, 7 y--l(1)1Bb-; male lethal, cell viable *Df(1)260-2 1B2-3;1B2-3 1, 4, 5 y--ac- sc+; male lethal, cell viable *Df(1)260-5 1A4-5;1A4-5 1, 4, 5 viable *Df(1)260-10 1A2-3;1A2-3 1, 4, 5 viable *Df(1)260-19 1A2-3;1A2-3 1, 4, 5 viable ( 1 = Demerec and Hoover, 1936, J. Hered. 27: 206-12; 2 = Ephrussi, 1934, Proc. Nat. Acad. Sci. USA 10: 420-22; 3 = Garcia-Bellido and Santamaria, 1978, Genetics 88: 469- 86; 4 = Sutton, 1940, Genetics 25: 628-35; 5 = Sutton, 1943, Genetics 28: 214; 6 = Walen, 1961, Genetics 46: 93- 103; 7 = White, Decelles, and Enlow, 1983, Genetics 104: 433-48. | Germ-line clones lethal (Garcia-Bellido and Robbins, 1983, Genetics 103: 235-47). Eliminates all external sense organs in embryo (Dambly-Chaudi`re and Ghysen, 1986, Wilhelm Roux's Arch. Dev. Biol. 195: 222-28). #*Df(1)262-*Df(1)354 origin: X ray induced. references: Patterson, 1932, Am. Naturalist 66: 193-206. genetics: Tabulated. deficiency genetics __________________________________ *Df(1)262 N *Df(1)267 N *Df(1)268 car- *Df(1)271 N *Df(1)274 f- *Df(1)303 N Df(1)306 y--ac- *Df(1)308 fa--ec- *Df(1)314 pn+ w--ec- bi+ *Df(1)354 pl- # Df(1)278.4B1 cytology: Df(1)2E3-F3;3A5-B4. discoverer: Wu. references: Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. 1985, Genetics 111: 23-41. genetics: Deficient for fs(1)K10 - l(1)3Ac. molecular biology: Breakpoint mapped to the DNA between +5.5 (Sal1 site) and +9.0 (EcoR1 site) by Haenlin, Steller, Pir- rotta, and Mohier, 1985, Cell 40: 827-37. # Df(1)306 origin: Induced by hybrid dysgenesis. references: Pelisson, 1981, Mol. Gen. Genet. 183: 123-29. genetics: Deficient for y and ac. # Df(1)403 cytology: Df(1)1A4 (or more complex rearrangement). Acts like a terminal deficiency for all loci distal to l(1)1Ac. synonym: l(1)403, Df(1)l(1)403. references: Maddern, 1977, DIS 52: 82. genetics: Exposes l(1)1Aa, l(1)1Ab and l(1)1Ac. Covered by BSYy+ but not by BSYy31d. # Df(1)724 cytology: Df(1)20D;20F. synonym: Df(1)l724. discoverer: Lifschytz. references: Ripoll and Garcia-Bellido, 1978, Genetics 91: 443-53. genetics: Zygotic lethal but cell viable in cuticle. # Df(1)733 cytology: Df(1)20D;20F. synonym: Df(1)l733. discoverer: Lifschytz. references: Ripoll and Garcia-Bellido, 1978, Genetics 91: 443-53. genetics: Zygotic lethal but cell viable in cuticle. # Df(1)1237 discoverer: Gans. references: Laurence, Johnson, and Struhl, 1983, Cell 35: 27- 34. genetics: Dominant female sterile (agametic); deficient for ovo. # Df(1)7108 cytology: {Df(1)19E1-2;20E-F}. references: Lifschytz and Yakobovitz, 1978, Mol. Gen. Genet. 161: 275-84. genetics: Deficient for run-su(f). Covered by y+Ymal+. # Df(1)A deficiency cytology origin ref ( genetics ________________________________________________________________________________ Df(1)A19 | 20;20F X ray 8, 9 wap--bb- Df(1)A23 1A1;1A6-7 X ray 7 l(1)1Aa--l(1)1Ac- Df(1)A33 20A;20F X ray 8, 9 l(1)20Ac--bb- Df(1)A53 19E5;20A1-2 X ray 3, 7 l(1)19Ed--eo- Df(1)A58 / X ray 9 mal--run- Df(1)A82 3D4-5;4E3 + X ray 5 l(1)EFa- In(1)12C6;14A8 Df(1)A94 1E4-5;2B11-12 X ray 3, 4, 5, 6, 7 fmf - Df(1)A113 3D6-E1;4F5 X ray 5, 7 slc--rb- Df(1)A118 /` 19E3-4;19E7-8 X ray 3, 6, 8, 9, shakB--vao- 10, 12, 13 Df(1)A122 cytologically normal X ray 8, 9, 12, 13 wap--l(1)20Ac- Df(1)A129 {20A3-20E} X ray 8, 9 wap--su(f)- Df(1)A209 | 20A;20F X ray 8, 9,11 l(1)20Ac--bb- or uncl--bb- Df(1)A211 {20A3;20E} X ray 8, 9 wap--su(f)- Df(1)At127 1E3-4;2A2-3 EMS 1, 2 l(1)1Ed--l(1)2Ad- ( 1 = Aizenzon and Belyaeva, 1982, DIS 58: 3-7; 2 = Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kramers, and Zhimu- lev, 1982, DIS 58: 184-90; 3 = Baird, Schalet, and Wyman, 1990, Genetics 126: 1045-59; 4 = Belyaeva, Aizenzon, Semeshin, Kiss, Koczka, Baritcheva, Gorelova, and Zhimulev, 1980, Chromosoma 81: 181-306; 5 = Craymer and Roy, 1980, DIS 55: 200-04; 6 = Kramers, Schalet, Paradi, and Huiser- Hoogteyling, 1983, Mutat. Res. 107: 187-201; 7 = Lefevre; 8 = Lifschytz, 1971, Mutat. Res. 13: 35-47; 9 = Lifschytz and Falk, 1968, Mutat. Res. 6: 235-44; 10 = Lifschytz and Yakobovitz, 1978, Mol. Gen. Genet. 161: 275-84; 11 = Rahman and Lindsley, 1981, Genetics 99: 49-64; 12 = Schalet and Lefevre, 1973, Chromosoma 44: 183-200; 13 = Schalet and Lefevre, 1976, The Genetics and Biology of Drosophila (Ash- burner and Novitski, eds.). Academic Press, London, New York, San Francisco, Vol. 1b, pp. 846-902. | Male sterile in combination with y+Ymal+ (Rahman and Linds- ley, 1981). / Df(1)A58/Df(1)A118 survives (Schalet and Lefevre, 1976) and shows vao. ` Df(1)16-3-35/Df(1)A118 survives (Schalet and Lefevre, 1976) and shows shakB (Baird). #*Df(1)A1: see Tp(1;4)A1 #*Df(1)A12: see T(1;2;4)A12 # Df(1)ac: Deficiency (1) achaete origin: X ray induced simultaneously with a detachment of an attached X marked with y. references: Muller, 1954, DIS 28: 146-47. genetics: Deficient for ac and probably y. Male viable. # Df(1)arth: Deficiency (1) arthritic origin: X ray induced in In(1)scS1Lsc8R In(1)dl-49 chromosome. discoverer: Schalet. references: Fleming, DeSimone, and White, 1989, Mol. Cell Biol. 9: 719-25. genetics: Deficient for arth-ac but not sc. Male and female viable. # Df(1)At127 cytology: Df(1)1E3-4;2A2-3. origin: Induced by ethyl methanesulfonate. references: Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kramers, and Zhimulev, 1982, DIS 58: 184-90. genetics: Deficient for l(1)1EFa-l(1)1EFj. # Df(1)B: Deficiency (1) Bar cytology: Df(1)15F9-16A1;16A6-7 superimposed on. Dp(1;1)15F9- 16A1;16A7-B1. All of the left 16A section and all but 16A7 of the right 16A section is included in the deficiency. Sutton (1943), confirmed by Peterson and Laughnan (1963), included f as if the left breakpoint were more distal than indicated. new order: 1 - 15F9|16A7 - 20. origin: X ray induced in B chromosome. discoverer: Demerec, 34a. synonym: Df(1)B263-20. references: Sutton, 1943, Genetics 28: 97-107 (fig.). Peterson and Laughnan, 1963, Proc. Nat. Acad. Sci. USA 50: 126-33. Laughnan, 1970, Mol. Gen. Genet. 108: 93-96. genetics: Reversion of B. Deficient for f-B. Male lethal. # Df(1)B12-Df(1)B264 origin: X ray induced. deficiency cytology ref ( genetics _________________________________________________________ Df(1)B12 | 19E1;20A1-2 1, 2, 4, 5 run--eo- Df(1)B18 20F;20F 2 includes bb Df(1)B47 / 20F;20F 2 includes bb Df(1)B57 19E1-2;19F1 1, 2, 3, 4, 6 run--unc- Df(1)B82 19F2-3;20F 1, 2 l(1)19Fb--bb- Df(1)B85 2 wap--bb- Df(1)B99 2 includes bb Df(1)B111 20A;20F 2 wap--bb- Df(1)B155 ` 2 eo--bb- Df(1)B179 - 2 Df(1)B182 2 includes bb Df(1)B199 2 Df(1)B225 2 Df(1)B255 2 Df(1)B264 2 wap--uncl- ( 1 = Falk, 1973, Mutat. Res. 20: 287-90; 2 = Lifschytz and Falk, 1968, Mutat. Res. 6: 235-44; 3 = Lifschytz and Falk, 1969, Genetics 62: 343-52; 4 = Lifschytz and Yakobovitz, 1978, Mol. Gen. Genet. 161: 275-84; 5 = Ripoll and Garcia- Bellido, 1979, Genetics 91: 443-53; 6 = Schalet and Lefevre, 1973, Chromosoma 44: 183-200. | Cell viable in cuticle. / Male sterile in combination with mal+Y. ` Also T(1;2). - Also T(1;3). # Df(1)B428 references: Fleming, DeSimone, and White, 1989, Mol. Cell Biol. 9: 719-25. genetics: Deficient for l(1)1Aa through ewg. # Df(1)Basc cytology: In(1)1B3-4;20FL1B2-3;20FR + In(1)6A1-3;10F10-11A1 + Df(1)1A1;1B2. Deficient for the euchromatin distal to the distal In(1)scS1 breakpoint of Basc. Origin probably analo- gous to that of Df(1)sc8. discoverer: Abrahamson. references: Simmons and Lim, 1980, Proc. Nat. Acad. Sci. USA 77: 6042-46. genetics: Recessive lethal. Covered by y+Y. # Df(1)bb: Deficiency (1) bobbed cytology: Deficiencies for most or all of the ribosomal cis- trons and neighboring heterochromatin; do not extend into regions not covered by the Y chromosome. origin: X ray induced. synonym: Df(1)bbl-. genetics: Deficient for bb. X/O male lethal. Segregates irregularly from the Y chromosome. Male sterile or nearly so in combination with T(Y;A)'s (Lindsley, Pearson, Rokop, Jones, and Stern, 1979, Genetics 91: s69-70) or with y+Ymal+ (Rahman and Lindsley, 1981). deficiency % proximal X ref ( heterochromatin deleted _________________________________________________ Df(1)bb3a 1 Df(1)bb74 48 1, 2 Df(1)bb158 | 82 1, 2, 3 Df(1)bb452 32 1, 2, 3 Df(1)bb456 72 1 *Df(1)bb481 / 1 ( 1 = Lindsley, Edington, and Von Halle, 1960, Genetics 45: 1649-70; 2 = Rahman and Lindsley, 1981, Genetics 99: 49-64; 3 = Yamamoto and Miklos, 1978, Chromosoma 66: 71-98. | According to Schalet, Df(1)bb158/Dp(1;f)18 and Df(1)bb158/Dp(1;f)122 males and Df(1)bb158/Df(1)mal3 females, all bb+, show eo phenotype in 50% of the flies, while Df(1)bb158/Df(1)17-137 females, all bb, show eo pheno- type in more than 50% of the flies. / Also carries In(1)481=In(1)12E-F;14B. # Df(1)bb-G: see In(1)sc4Lsc8R # Df(1)bi: Deficiency (1) bifid references: Banga, Bloomquist, Brodberg, Pye, Larrivee, Mason, Boyd, and Pak, 1986, Chromosoma 93: 341-46. Oliver, Perrimon, and Mahowald, 1988, Genetics 120: 159-71. genetics: Deficient for bi. deficiency cytology origin genetics ______________________________________________________ Df(1)bi-D1 ( 4B3-4;4D1-2 X ray mei9--amb- Df(1)bi-D2 | 4B6-C1;4D7-E1 X ray lac--svb- Df(1)bi-D3 / 4C5-6;4C7-8 X ray lac--amb- Df(1)bi-D4 not visible X ray bi--amb- Df(1)bi-DL1 4A3-5;4C15-16 Uc mutator mei9--amb- Df(1)bi-DL2 4B3-4;4C15-D1 Uc mutator mei9--amb- Df(1)bi-DL3 3C7-12;4E1-2 Uc mutator bi--rg- Df(1)bi-DL4 4B1-2;4C15-D1 Uc mutator mei9--amb- Df(1)bi-DL5 3C7-12;4E1-2 Uc mutator bi--svb- Df(1)bi-DL6 4B1-2;4C15-16 Uc mutator mei9--amb- Df(1)bi-DL7 4A3-5;4C15-D1 Uc mutator mei9--amb- Df(1)bi-RC40 see Df(1)RC40 ( Includes mei-9. | Includes norpA. / Includes amb. # Df(1)br26 cytology: Df(1)1D-E;2B5. origin: Induced by DEB. references: Kiss, Beaton, Tardiff, Fristrom, and Fristrom, 1988, Genetics 118: 247-59. genetics: Deficient for br. # Df(1)br-rv1 cytology: Df(1)2B3;2B4. origin: X ray induced. references: Belyaeva, Protopopov, Baricheva, Semeshin, Izquierdo, and Zhimulev, 1987, Chromosoma 95: 295-310. genetics: Deficient for sta and br. # Df(1)C1-Df(1)C10 origin: X ray induced in In(1)wm51b. genetics: Deficient for su(f). deficiency cytology ref ( ______________________________________________ Df(1)C1 | 19E2-3;19E2-3 1, 2, 3 Df(1)C2 20E-F + T(1;2)3C2;34A-B 2 Df(1)C3 / 20A;20A 2, 3 Df(1)C4 20A;20A 1, 2, 3 Df(1)C5 19E4-8;19E4-8 2 Df(1)C6 20A;20A 2 Df(1)C7 20A;20A 2 Df(1)C10 20A;20A 2 ( 1 = Appels and Hilliker, 1982, Genet. Res. 39: 149-56; 2 = Hilliker and Appels, 1982, Chromosoma 86: 469-90; 3 = Pimpinelli, Sullivan, Prout, and Sandler, 1985, Genetics 109: 701-24. | Deletes ABO and DAL (Pimpinelli et al., 1985). / Deletes ABO but not DAL (Pimpinelli et al., 1985). #*Df(1)C15-Df(1)C246 origin: X ray induced. discoverer: Lefevre. deficiency cytology ref ( genetics ______________________________________________________________________ *Df(1)C15 1B14-C1;2A3 4, 6 mul--l(1)2Ad- Df(1)C52 | 8E;9C-D 1, 2, 4-6, 10, 12 mus(1)109- flw+ Df(1)C60 1A4;1A6 6, 11 l(1)1Ac-; cell viable in abdomen Df(1)C74 19F1;20A4 8, 9 lfl--intro- Df(1)C128 / 7D1;7D5-6 4-7, 11 sn--mys- Df(1)C149 5A8-9;5C5-6 1, 2, 4, 6, 12 cv--mus(1)105- rux+ Df(1)C159 3F1;4F14 6 Df(1)C237 19F;20 6 lfl--su(f)- Df(1)C246 `- 11D-E;12A1-2 3, 4, 6, 12 wy--s- slight M ( 1 = Baker and Smith, 1979, Genetics 92: 833-47; 2 = Baker, Smith, and Gatti, 1982, Proc. Nat. Acad. Sci. USA 79: 1205-09; 3 = Brown and Voelker, 1980, Biochem. Genet. 18: 303-09; 4 = Craymer and Roy, 1980, DIS 55: 200-04; 5 = Deak, Bellamy, Bienz, Dubuis, Fenner, Gollin, Rahmi, Ramp, Reinhardt, and Cotton, 1982, J. Embryol. Exp. Morphol. 69: 61-81; 6 = Lefevre; 7 = Lefevre and Johnson, 1973, Genetics 74: 633-45; 8 = Perrimon, Engstrom, and Mahowald, 1989, Genetics 121: 333-52. 9 = Perrimon, Smouse, and Mik- los, 1989, Genetics 121: 313-31. 10 = Postlethwait and Shirk, 1981, Amer. Zool. 21: 687-700; 11 = Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53; 12 = Wieschaus, Nusslein-Volhard and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307. | Mutant wing position of fliF and flw uncovered in deficiency heterozygotes. / Synonym: Df(1)snC128. High frequency of homeotic transformations found in Df(3)red/+ progeny of Df(1)C128/+ females (Gans, Forquignon, and Masson, 1980, Genetics 96: 887-902). Lethal in germ-line clones (Garcia-Bellido and Robbins, 1983, Genetics 103: 235-47). ` Seems to include locus involved in early step of sex deter- mination (Scott and Baker, 1986, Genetics 113: s35). - YSX.YL, Df(1)C246, In(1)EN, y M/YSX.YL, Df(1)gl In(1)EN, y g f B females are viable, yellow, and minute (Schalet). # Df(1)c99-wm4 cytology: Df(1)2E1-2;3C1-2. discoverer: Lefevre. references: Perrimon, Engstrom, and Mahowald, 1985, Genetics 111: 23-41. #*Df(1)C-PL: Deficiency (1) C of Peterson and Laughnan cytology: Df(1)15F;16E. origin: Spontaneous; allegedly an asymmetrical exchange. discoverer: Peterson and Laughnan. references: 1963, Proc. Nat. Acad. Sci. USA 50: 126-33. genetics: Deficient for f and B but not os. Male lethal. # Df(1)cho: Deficiency (1) chocolate reference: Steinmann-Zwicky, 1988, EMBO J. 7: 3889-98. deficiency cytology genetics ________________________________________ Df(1)cho2 3E;4A mdl- bi+ Df(1)cho3 3C;3F cho- mdl+ Df(1)cho5 3D;4A cho- mdl+ Df(1)cho6 1F;4A mdl- bi+ Df(1)cho7 2E-F;4B mdl- bi+ Df(1)cho8 3C;4A mdl- bi+ Df(1)cho10 cho- mdl+ Df(1)cho19 3F;4F ec--fs(1)A1621- Df(1)cho23 3E-F;4F fl(1)302- ovo+ Df(1)cho24 mdl- bi+ Df(1)cho25 mdl- bi+ # Df(1)cin-arth: Deficiency (1) cinnamon-arthritic references: Kramers, Schalet, Paradi, and Huiser-Hooteyling, 1983, Mutat. Res. 107: 187-201. genetics: Deficient for l(1)1A through sc. # Df(1)ClLbbDfR: see In(1)ClLbbDfR # Df(1)ClLy4R: see In(1)ClLy4R # Df(1)cm: Deficiency (1) carmine origin: X ray induced. genetics: Deficient for cm. deficiency cytology discoverer ref ( ________________________________________________ *Df(1)cm-D5 6E5-6;6F2-3 DeFrank 1 *Df(1)cm-H2 6D8-E1;6E6-F1 Hannah 1 *Df(1)cm-H4 6D8-E1;6E6-F1 Hannah 1 Df(1)cm-R8 6E;6E 2 ( 1 = CP627; 2 = Valencia, 1966, DIS 41: 58. # Df(1)cm-In: see In(1)cm-df # In(1)ct: Inversion (1) cut origin: X ray induced. genetics: All male lethal except for In(1)ct43aH1 and In(1)ctJ7 (semilethal). In(1)ct3a2 and In(1)ctJ7 give extreme ct in combination with ct6. inversion cytology ref ( ________________________________________________ *In(1)ct3a2 7B;20 2, 3 *In(1)ct3b1 3A4-B1;7B2-5 2 *In(1)ct12a2 4E2-3;7B2-4 1 *In(1)ct13a1 7B2-3;19-20 2 *In(1)ct14a3 7B2-3;20 2 *In(1)ct14b2 3D2-5;7B2-4 2 In(1)ct43aH1 4B1-4;7B4-C1 + 7 10D5-6;20F *In(1)ct268-13 | 2E3-F1;2F2-3;7B2-3; 4, 5 7B4-5;19A4-5;19A6-B1 superimposed on R(1)1A3-4;19F-20A1 (2F1-2,7B3-4,19A5-6 missing) *In(1)ct268-18 / 7B2-3;7B4-5;11D8-9 5 (7B3-4 missing) *In(1)ct268-20 ` 6F11-7A1;7B3;10B11-12 5 (7A1-B5 missing) *In(1)ct268-27 3D6-E1;7B3-5 5 *In(1)ctJ7 7B3-4;7D22 6 *In(1)ctJ12 7B3-4;7D4 6 *In(1)ctJ13 5A;7B3-4 6 ( 1 = De Frank; 2 = Hannah-Alava; 3 = Hannah-Alava, 1971, Mol. Gen. Genet. 113: 191-203; 4 = Hoover, 1937, Genetics 22: 634-40; 5 = Hoover, 1938, Z. Indukt. Abstamm. Verer- bungsl. 74: 420-34; 6 = Lefevre and Johnson, 1973, Genetics 74: 633-46; 7 = Valencia, 1966, DIS 41: 58. | New order: |1A1 - 2E3|7B2 -2F3 |19A4 - 7B5 |19B1 - 20.20 - 20A1|. / New order: 1A - 7B2|11D8 -7B5|11D9 - 20. ` New order: 1A - 6F11|10B11 -7B6|10B12 - 20. # Df(1)ct78 cytology: Df(1)6F1-2;7C1-2. origin: Derived from unstable X chromosome. references: Lim, 1979, Genetics 93: 681-701. Raymond, Laverty, and Simmons, 1986, DIS 63: 111-14. genetics: Deficient for ct. #*Df(1)ct268-13: see In(1)ct268-13 #*Df(1)ct268-18: see In(1)ct268-18 #*Df(1)ct268-20: see In(1)ct268-20 #*Df(1)ct268-30 cytology: Df(1)7B2-3;7C3-4. origin: X ray induced. discoverer: Hoover, 38d. references: CP627. genetics: Deficient for ct but not scp or sn. #*Df(1)ct268-37: see Tp(1;3)ct268-37 # Df(1)ct268-42 cytology: Df(1)7A5-6;7B8-C1 (Sutton). origin: X ray induced. discoverer: Demerec, 40a. references: CP627. Homyk and Pye, 1989, J. Neurogenet. 5: 37-48. genetics: Deficient for ct to rex but not cm, scp, or sn. # Df(1)ct-J4 cytology: Df(1)7A2-3;7C1. origin: X ray induced in In(1)dl-49. discoverer: T.K. Johnson. references: Lefevre and Johnson, 1973, Genetics 74: 633-45. Johnson and Judd, 1979, Genetics 92: 485-502. Craymer and Roy, 1980, DIS 55: 200-04. Homyk and Pye, 1989, J. Neurogenet. 5: 37-48. genetics: Deficient for ct and rex but not shf. Lethal male embryos show incomplete condensation of the ventral nerve cord [Campos-Ortega and Jimenez, 1979, Development and Neurobiology of Drosophila (Siddiqi, Babu, Hall, and Hall, eds.). Plenum Press, New York and London, pp. 201-22]. Heterozygotes with wild-type or balancer X chromosomes show thoracic protuber- ances [100% penetrance and variable expression (Voelker and Wisely, 1982, DIS 58: 150-51)]. # Df(1)ct-J6 cytology: Df(1)6E1;7C1. origin: X ray induced. discoverer: T.K. Johnson. references: Lefevre and Johnson, 1973, Genetics 74: 633-45. Craymer and Roy, 1980, DIS 55: 200-04. Homyk and Pye, 1989, J. Neurogenet. 5: 37-48. genetics: Deficient for ct but not rex. Heterozygotes show thoracic protuberances as in Df(1)ct-J4. # Df(1)(D): see Df(1)r-D1 # Df(1)D7 cytology: Df(1)14C7-D1;14E3-F1. synonym: Df(1)l-D7. references: Ganetzky, 1984, Genetics 108: 897-911. genetics: Uncovers para. # Df(1)D17: see Df(1)r-D17 # Df(1)D34 cytology: Df(1)14F1-2;14F6 (Lefevre). origin: X ray induced. discoverer: M.M. Green. synonym: Df(1)l-D34. references: Jarry, 1979, Mol. Gen. Genet. 172: 199-202. Ganetzky, 1984, Genetics 108: 897-911. genetics: Uncovers several lethal complementation groups including para but does not include r. # Df(1)D43L1 cytology: Df(1)19E8;20E-F. origin: Cs137 induced. discoverer: Himoe. references: Schalet and Finnerty, 1968, DIS 43: 128-29. Schalet and Lefevre, 1973, Chromosoma 44: 183-200. Rahman and Lindsley, 1981, Genetics 99: 49-64. genetics: Deficient for unc-su(f). # Df(1)DA622 cytology: Df(1)10B8;10D2. discoverer: Lefevre. genetics: Deficient for dlg. # Df(1)DCB1-35b cytology: Df(1)19F1-2;20E-F. origin: Induced by tritiated deoxycytidine. discoverer: Kaplan. references: Schalet and Finnerty, 1968, DIS 43: 128-29. Schalet and Lefevre, 1973, Chromosoma 44: 183-200. Craymer and Roy, 1980, DIS 55: 200-04. genetics: Deficient for lfl-su(f) but not run (Gergen and Wieschaus, 1986, Cell 45: 289-99). #*Df(1)DCB1-35c cytology: Cytologically normal. origin: Induced by tritiated deoxycytidine. discoverer: Kaplan. references: Schalet and Finnerty, 1968, DIS 43: 128-29. Schalet and Lefevre, 1973, Chromosoma 44: 183-200. genetics: Deficient for wap and intro. # Df(1)Del lz A: see *In(1)lzA # Df(1)Del271b: see *T(1;2)271b # Df(1)dm75e19: Deficiency (1) diminutive cytology: Df(1)3C11;3E4 superimposed on In(1)3E;5E. origin: X ray induced. discoverer: Lefevre. synonym: Df(1)HA44. references: Craymer and Roy, 1980, DIS 55: 200-04. McGinnis, Farrell, and Beckendorf, 1980, Proc. Nat. Acad. Sci. USA 77: 7367-71. Byers, Davis, and Kiger, 1981, Nature 289: 79-81. Davis and Davidson, 1984, Mol. Cell. Biol. 4: 358-67. genetics: Deficient for dnc-slc but not Sgs-4 (McGinnis et al., 1980). Cell viable in abdominal cuticle (Ripoll and Garcia- Bellido, 1979, Genetics 91: 443-53). Slight dm phenotype in heterozygotes with Ubl (Mortin and Lefevre, 1981, Chromosoma 82: 237-47). Germ-line clones lethal (Garcia-Bellido and Robbins, 1983, Genetics 103: 235-47). genetics: Deficient for dnc - slc. molecular biology: Left breakpoint located on molecular map (McGinnis et al., 1980; Davis and Davidson, 1984). # Df(1)dm77h cytology: Df(1)3D5;3F8-9. origin: X ray induced. discoverer: Lefevre. references: Davis and Davidson, 1984, Mol. Cell. Biol. 4: 358-67. genetics: Deficient for dm but not dnc. # Df(1)dor1T: Deficiency (1) deep orange cytology: Df(1)1E3-4;2B17-18. origin: / ray induced. discoverer: Gorelova. references: Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kramers, and Zhimulev, 1982, DIS 58: 184-90. genetics: Deficient for dor. # Df(1)dor2T cytology: Df(1)2B6;2E1-2. origin: / ray induced. discoverer: Gorelova. references: Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kramers, and Zhimulev, 1982, DIS 58: 184-90. genetics: Deficient for dor. # Df(1)dor-A94: see Df(1)A94 # Df(1)DV4: see T(1;4)wmDV4 # Df(1)E128 cytology: Df(1)17C;18A. origin: Induced by hybrid dysgenesis. references: Engels and Preston, 1984, Genetics 107: 657-78. genetics: Deficient for Bx and hdp - b. # Df(1)E150 cytology: Df(1)14B3-4;14E. references: Kulkarni, Steinlauf, and Hall, 1988, Genetics 118: 267-85. genetics: Deficient for diss. # Df(1)E160.1 cytology: Df(1)17A;18A2. origin: Induced by hybrid dysgenesis. references: Engels and Preston, 1984, Genetics 107: 657-78. genetics: Deficient for Bx and hdp - b. # Df(1)EA113 cytology: Df(1)20A;20E. origin: Induced by ethyl methanesulfonate. references: Perrimon, Smouse, and Miklos, 1989, Genetics 121: 313-31. genetics: Deficient for uncl-su(f). # Df(1)EH653 cytology: Df(1)19A2-3;20A-B. origin: Induced by ethyl methanesulfonate. references: Eberl and Hilliker, 1988, Genetics 118: 109-20. genetics: Deficient for run and fog, but not for bb. # Df(1)f: Deficiency (1) forked origin: X ray induced. synonym: Df(1)f257. deficiency cytology discoverer ref ( genetics _________________________________________________________________________ Df(1)f257-5 15E7-F1;15F2-4 Demerec, 33k 1 M+ f- os+ *Df(1)f257-6 15E4-F1;16A1 Bridges, 1917 1, 2 M+ f- B- os+ *Df(1)f257-9 15E7-F1;16D2-4 | Demerec, 34c 1, 2 M+ f- B- lh+ *Df(1)f257-27 14F6-15A1;15F5-6 | Demerec, 38l 1 M(1)15D- f- *Df(1)f257-28 15E7-F1;16E5-F1 | Sutton, 40h 1 f- B- *Df(1)f257-31 15E7-F1;15F5-6 Bishop, 41a 1 M+ f- os+ ( 1 = CP627; 2 = Sutton, 1943, Genetics 28: 97-107. | Superimposed on Dp(1;1)B = Dp(1;1)15F9-16A1;16A7-B1. # Df(1)fa-swb: Deficiency (1) facet-strawberry cytology: Interband deletion between 3C5-6 and 3C7 such that 3C5-6 ("fused" to 3C7) appears thick, while 3C7 appears to be missing. origin: X ray induced. discoverer: Lefevre and Kelley. synonym: swb71b (Lefevre and Kelley, 1972, DIS 48: 146-47); faswb71b (Ashburner). references: Welshons and Keppy, 1975, Genetics 80: 143-55. Keppy and Welshons, 1977, Genetics 85: 497-506. 1980, Chromosoma 76: 191-200. genetics: Eye color strawberrylike (but more mottled) and eye surface rougher than in faswb62b (= swb62b of Ives, 1969, DIS 44: 46). # Df(1)FM7 cytology: Df(1)1A;1B2-3. origin: X ray induced. discoverer: Gyurkovics and Voelker. references: Voelker, Greenleaf, Gyurkovics, Wisely, Huang and Searles, 1984, Genetics 107: 279-84. genetics: Deficient for genes from X tip through ac. # Df(1)fu: Deficiency (1) fused genetics: Deficient for fu. lethal Rescue deficiency cytology origin ref ( stage by Dp | _______________________________________________________________________ Df(1)fu3 17C3-7;17D1-2 DEB 1 larva + Df(1)fu5 17B;17E-F DEB 1 - Df(1)fu13 17C3-7;17D1-2 X ray 2 + Df(1)fu15 17C;17D+In(1)12F;17F DEB 1 embryo - Df(1)fu-A7 17C;18A DEB 1 embryo - Df(1)fu-B10 17C;18A-B DEB 1 - Df(1)fu-BX14 17A;17D1-2 X ray 1 embryo - Df(1)fu-C3 / 17A;18B Df(1)fu-E5 17C;17E-F DEB 1 - Df(1)fu-H4 17C3-7;17D1-2 DEB 1 larva + Df(1)fu-I3 17A;18B DEB 1 - Df(1)fu-PI 17C3-7;17D1-2 HD 2 larva + Df(1)fu-S4 17C;17E-F DEB 1 - Df(1)fu-Z4 {17C4-6;17C4-6} DEB 1 larva + ( 1 = Busson, Limbourg-Bouchon, Mariol, Preat, and Lamour- Isnard, 1988, Roux's Arch. Dev. Biol. 197: 221-30. 2 = Holmgren (unpublished). | Dp(1;3)fu+10. / See Ashburner for further information. # Df(1)fw-HF368: see Df(1)HF368 # Df(1)g70e cytology: Df(1)17A3-4;17C6-7. origin: Induced by mutator gene mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. # Df(1)g-HA92: see Df(1)HA92 # Df(1)g: Deficiency (1) garnet cytology: Df(1)12A;12E (Nicoletti). origin: Spontaneous. discoverer: L. V. Morgan, 24l24. references: Mason, Green, Shaw, and Boyd, 1981, Mutat. Res. 81: 329-43. Waring, DiOrio, and Hennen, 1983, Dev. Biol. 100: 452-63. genetics: Deficient for g, l(1)dd4, ty and ben but not wy, s, na, pl, or sd. Uncovers mus(1)101D1 (Mason et al., 1981). Lethal in male and cell lethal. # Df(1)g2 cytology: Df(1)12A;12C. origin: X ray induced in In(1)sc29. discoverer: Schalet. genetics: Deficient for mus101, g, l(1)dd4, ty, rdgB, but not ben, or na. Covered by Dp(1;5)LJ9. Complements Df(1)C246 = Df(1)11D;12A1-2. # Df(1)/2: Deficiency (1) gamma cytology: Df(1)7D14;8A3. references: Wakimoto and Spradling, 1981-82, Year Book, Carne- gie Inst. Washington 81: 190-91. Homyk and Pye, 1989, J. Neurogenet. 5: 37-48. genetics: sesD+. # Df(1)/a3 cytology: Df(1)7D4;8A3. references: Wakimoto and Spradling, 1981-82, Year Book - Carne- gie Inst. Washington 81: 190-91. # Df(1)GA origin: X ray induced. discoverer: Lefevre. deficiency cytology ref ( genetics _____________________________________________________________ Df(1)GA22 20;20 5 wap-- su(f)- Df(1)GA33 19F;20 2,5 unc-- uncl- Df(1)GA34 7A4-5;7B3-4 2,4 l(1)7Ab-- l(1)7Bb- Df(1)GA37 19E;19F 2,4,5 run-- l(1)19Fg- Df(1)GA40 19E;20F 2,5 run-- su(f)- Df(1)GA42 | 20B1;20F 6 fog-- bb- Df(1)GA56 4C5-6;4D1 1 omb-- hnt- svb+ Df(1)GA90 20C;20F 5,6 l(1)20Cb-- bb- Df(1)GA102 3D4-5;3F7-8 9 slc-, cho- ec+ Df(1)GA104 19F;19F 5 fli-- l(1)19Fg- Df(1)GA112 / ` 10A11-B1;10C2 8,9 l(1)10Ag-- l(1)10Cd- Df(1)GA113 3D6-E1;? 2 slc- Df(1)GA120 2 Df(1)GA131 20;20 5 sph-- su(f)- ( 1 = Lawlor, 1980, DIS 55: 81-82; 2 = Lefevre; 3 = Miklos, Kelly, Combe, Leeds, and Lefevre, 1987, J. Neurogenet. 4: 1-19; 4 = Perrimon, Engstrom, and Mahowald, 1989, Genet- ics 121: 333-52; 5 = Perrimon, Smouse, and Miklos, 1989, Genetics 121: 313-31; 6 = Rahman and Lindsley, 1980, DIS 45: 123-24; 7 = Rahman and Lindsley, 1981, Genetics 99: 49-64; 8 = Voelker, Wisely, Huang, and Gyurkovics, 1985, Mol. Gen. Genet. 201: 437-45; 9 = Wieschaus, Nusslein-Volhard and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307. | Associated with a T(1;2). / Df(1)HA85/Df(1)GA112 and Df(1)m259-4/Df(1)GA112 females sur- vive to adulthood and show no mutant phenotype (Voelker et al., 1985). ` Right DNA breakpoint 16.5 kb to the left of the origin of the RpII215 walk of Biggs, Searles, and Greenleaf, 1985, Cell 2: 611-21 ("+" values to the right and "-" values to the left). # Df(1)GAM201 cytology: Df(1)3A2-3;3C2-3. origin: X ray induced. discoverer: Lefevre. references: Perrimon, Engstrom, and Mahowald, 1989, Genetics 121: 333-52. genetics: Deficient for z - w. # Df(1)GE202 cytology: Df(1)7D12-13;7E3-4. origin: X ray induced. discoverer: Lefevre. genetics: Deficient for l(1)7Dj - l(1)7Ea. # Df(1)GE261 cytology: Df(1)1A1;1B10-11. origin: X ray induced. discoverer: Lefevre. genetics: Deficient for l(1)1Aa - vnd. # Df(1)GE263 cytology: Df(1)19F1-2;20A1-2. origin: X ray induced. references: Perrimon, Smouse, and Miklos, 1989, Genetics 121: 313-31. genetics: Deficient for fliI - eo. # Df(1)h70e cytology: Df(1)1A1;1B6. origin: Induced by mutator gene mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. # Df(1)HA11 - Df(1)HF396 origin: X ray induced. discoverer: Lefevre. deficiency cytology ref ( genetics _____________________________________________________________________ Df(1)HA11 7D13-14;7D22 3, 4, 6 l(1)adl1-- lon- otu+ Df(1)HA18 not visible 6 l(1)2Ab-- sta- Df(1)HA32 6E4-5;7A6 1, 6 shf+ cm- scp+ Df(1)HA44 see Df(1)dm75e19 Df(1)HA52 12E5;13A4 Df(1)HA85 10C1-2;11A1-2 1 tyl+ dy- Df(1)HA92 | 12A6-7;12D3 1, 6, 7, 8 s+ g-- ty- l(1)dd4- rdgB- ben- na+ Df(1)HA326 includes 19F 11 seg- Df(1)HC133 / 9B9-10;9E-F 1, 6, 12 flw-- fliK- sbr+ Df(1)HC163 ` 4A1-2;4D1-2 1, 5 mei-9-- rb- Df(1)HC163B - 4B1-2;4F1-2 5 mei-9-- rb- Df(1)HC194 3A1;3C3-4 6, 8a gt-- w- rst+ Df(1)HC244 3E8;4F11-12 1, 5, 6 ec-- rg- cx+ Df(1)HC279 6 shakB-- vao- Df(1)HE333 not visible sta-- dor- Df(1)HF334 19C3;20E-F 2 mal-- su(f)- bb+ *Df(1)HF349 13B5;13E1 1, 6 Df(1)HF359 {20A-B;20E} 6 l(1)20Bb-- su(f)- Df(1)HF366 3E7-8;5A7 1, 6, 10 ec-- rg- bo+ Df(1)HF368 11A2;11B9 1, 8, 9 fw-- Lsp1(- Df(1)HF394 13B5;13E1 1, 8 sd- Df(1)HF396 18E1-2;20 1, 6 sw-- su(f)- Df(1)HF406 3C4-5;? rst- ( 1 = Craymer and Roy, 1980, DIS 55: 200-04; 2 = Durica and Krider, 1978, Genetics 89: 37-64; 3 = Homyk and Emer- son, 1985, Genetics 110: s92; 4 = King and Riley, 1982, Dev. Genet. 3: 69-89; 5 = Lawlor, 1980, DIS 80: 81-82; 6 = Lefevre; 7 = Mason, Green, Shaw, and Boyd, 1981, Mutat. Res. 81: 329-43; 8 = Mortin and Lefevre, 1981, Chromosoma 82: 237-47; 8a = Perrimon, Engstrom, and Mahowald, 1989, Genetics 121: 333-52; 9 = Roberts and Evans-Roberts, 1979, Nature 280: 691-92; 10 = Sodja, Rizki, Rizki and Zafar, 1982, Chromosoma 86: 293-98; 11 = Wieschaus, Audit, and Masson, 1981, Dev. Biol. 88: 92-103. 12 = Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Khudyakov, Patzevich, Semeshin, Baritcheva, Aizen- zon, Kramers, and Eakin, 1982, DIS 58: 210-14; | Synonym: Df(1)gHA92. Deficiency uncovers mus(1)101 (Mason et al., 1981). / Listed as Df(1)HC163 by Craymer and Roy, 1980. ` Deficiency lost according to Craymer and Roy, 1980. - Lethal segregant from Df(1)HC163 or Df(1)RC40 (Lawlor, 1980). Synonym: Df(1)fwHF368. # Df(1)Hk. Deficiency (1) Hyperkinetic cytology: Df(1)9A;9C. origin: X ray induced. discoverer: Schlimgen and Kreber. synonym: Df(1)Hk__R2. references: Stern and Ganetsky, 1989, J. Neurogenet. 5: 215- 28. genetics: Deficient for Hk. # Df(1)HM: Deficiency (1) Hycanthon Methanesulfonate origin: Induced by hycanthon methanesulfonate. deficiency cytology ref ( genetics ______________________________________________________ Df(1)HM3 3A;3B-C 2 l(1)3Ac-- l(1)3Bf - Df(1)HM5 20A-B;20? 2 fog-- ? Df(1)HM8 20A-B;20? 2 fog-- ? Df(1)HM15 1 ras- Df(1)HM44 19B;19F5-6 2,3 sw-- l(1)19Ff - Df(1)HM45 19D-E;20? 2 run-- ? Df(1)HM47 20A-B;20? 2 fog-- ? Df(1)HM49 19E-F;20A 2 lfl-- wap- Df(1)HM50 19E-F;20A 2 lfl-- wap- Df(1)HM406 3A;3C 2 l(1)3Ad-- rst- Df(1)HM407 20B;20? 2 stn-- ? Df(1)HM418 20A;20? 2 wap-- ? Df(1)HM422 20A;20? 2 wap-- ? Df(1)HM428 1A;1A-B 2 l(1)1Ad-- ewg- Df(1)HM430 20A-B;20C-D 2 wap-- l(1)20Cb- Df(1)HM444 20A-B;20? 2 fog-- ? Df(1)HM455 20A;20? 2 wap-- ? Df(1)HM456 10B;10C-D 2,4 l(1)10A-- l(1)10Ce- Df(1)HM458 2F-3A;3A 2 l(1)3Ad-- ? Df(1)HM459 1 ct-- g Df(1)HM460 3A 2 mit(1)15-- ? ( 1 = Ashburner; 2 = Kramers, Schalet, Paradi, and Huiser- Hoogteyling, 1983 , Mutat . Res. 107: 187-201; 3 = Miklos, Kramers, and Schalet, 1986, DIS 63: 96-97; 4 = Voelker, Wisely, Huang, and Gyurkovics, 1985, Mol. Gen. Genet. 201: 437-45. # Df(1)i70e cytology: X proximal. origin: Induced by mutator gene mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. # Df(1)J1-259: see Df(1)259 # Df(1)JA, JC and JF origin: X ray induced. discoverer: Lefevre. deficiency cytology ref ( genetics ________________________________________________________________ Df(1)JA21 19E5-6;20 4 *Df(1)JA22 9F13;10A1 4 v- Df(1)JA26 11A1;11D-E 1, 4 fw- wy+ Df(1)JA27 18A5;18D1-2 1, 6 car+; fog-- su(f)- Df(1)JA52 2C10-D1;2D3-4 4, 5 usp+ Actn--pha- Pgd+ Df(1)JA53 3D4-5;3E7 dm- l(3)3Ee- Df(1)JA68 Df(1)JA117 19F;19F 6 l(3)19Ff - l(3)19Fg- *Df(1)JA118 | 10F11;11C-D + 4,7 fw- 19F1;20A1-2 tuh-1 - Df(1)JC4 20A1;20E-F 1, 4, 7 eo-- su(f)- Df(1)JC12 4 eo-- su(f)- Df(1)JC19 2F6;3C5 1,3,4,5 pn+ gt-- rst- Df(1)JC37 19E2;20A2 4 Df(1)JC70 4C15-16;5A1-2 1, 4 rb+ rg- cx+ Df(1)JC77 19F;20 6 l(1)19Ff -- eo- Df(1)JC102 19E5-7;20A2 4, 8 cell lethal in cuticle Df(1)JC105 2D4-6;2D4-6 4, 5 Pgd+ wapl -- l(1)2Ea- Df(1)JF4 19E7;20A 4 pcx+ Df(1)JF5 / 5E5-6;5E6-7 4, 9 swa- ( 1 = Craymer and Roy, 1980, DIS 55: 200-04; 2 = Dura, Randscholt, Deatrick, Erk, Santamaria, Freeman, Freeman, Weddell, and Brock, 1987, Cell 51: 829-39; 3 = Honisch and Campos-Ortega, 1982, DIS 58: 76; 4 = Lefevre; 5 = Perrimon, Engstrom, and Mahowald, 1985, Genetics 111: 23-41; 6 = Per- rimon, Smouse, and Miklos, 1989, Genetics 121: 313-31; 7 = Pyati, 1976, Mol. Gen. Genet. 146: 189-90; 8 = Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53; 9 = Stephen- son and Mahowald, 1987, Dev. Biol. 124: 1-8. | Double deficiency. / Induced by diepoxybutane. # Df(1)K5: Deficiency (1) of Kennison origin: X ray induced. discoverer: Kennison. references: Rahman and Lindsley, 1981, Genetics 99: 49-64. genetics: fog+ l(1)20Cb--bb-. # Df(1)K95 cytology: Df(1)3A3-4;3B1-2. origin: X ray induced. discoverer: Falk. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82. genetics: Deficient for l(1)3Ac - l(1)3Ba. Cell lethal in cuticle and in germ-line clones (Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53). Male lethal in embryo. molecular biology: Associated with 30kb inversion to right of the deletion (Reddy, Zehring, Wheeler, Pirrotta, Hadfield, Hall, and Rosbach, 1984, Cell 38: 701-10). Left breakpoint localized to an approximately 4 kilobase restriction fragment some 70 kb to the right of the origin of a 160 kb walk (Gunaratne, Mansukhani, Lipari, Liou, Martindale, and Gold- berg, 1986, Proc. Nat. Acad. Sci. USA 83: 701-05). # Df(1)KA1-Df(1)KC10 origin: X ray induced. discoverer: Lefevre. deficiency cytology ref ( genetics _______________________________________________________________________ Df(1)KA1 19E5;20E-F 4, 5, 8 Df(1)KA6 10E1;11A7-8 2, 5, 8 m--fw- rtv+ Df(1)KA7 | 10A9;10F6-7 2, 5, 6, 8, 9 l(1)10Ag+ dsh--ftd- tsg+ Df(1)KA9 / 12E1;13A5 1, 2, 4, 8 ty+ na-; incomplete condensation and splitting of ventral nerve cord in hemizygous embryos Df(1)KA10 ` 11A1;11A7-8 1, 2 ,8 fw--tsg-; duplicated ventral nerve cord in hemizygous embryos; cell lethal Df(1)KA14 ` 7F1-2;8C6 2, 3, 5, 8 lon+ otu--ptg-; includes oc Df(1)KC10 20C;20D 7, 8 l(1)20Ca--l(1)20Cb-; cell viable in cuticle ( 1 = Campos-Ortega and Jimenez, 1980, Development and Neuro- biology of Drosophila (Siddiqi, Babu, Hall, and Hall, eds.), Plenum Press, New York and London, pp. 201-22; 2 = Craymer and Roy, 1980, DIS 55: 200-04; 3 = King and Riley, 1982, Dev. Genet. (Amsterdam) 3: 69-89; 4 = Lefevre; 5 = Kreber and Ganetzky; 6 = Mortin and Lefevre, 1981, Chromosoma 82: 237-47; 7 = Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53; 8 = Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307. 9 = Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bga- tov, Khyudyakov, Patzevich, Semeshin, Baritcheva, Aizenzon, Kramers, and Eeken, 1982, DIS 58: 210-14. | Synonym: Df(1)m-KA7. / Also includes rut (Livingston, Sziber, and Quinn, 1984, Cell 37: 205-15). ` Germ-line clones lethal (Garcia-Bellido and Robbins, 1983, Genetics 103: 235-47). # Df(1)L10 cytology: Df(1)1A1;1A6-7. origin: X ray induced. discoverer: Lefevre. genetics: Deficient for l(1)1Aa - l(1)1Ac. # Df(1)l24 references: Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. 1985, Genetics 111: 23-41. genetics: Deficient for pn through l(1)2Ea. # Df(1)l32 cytology: Df(1)14B17-C1;15A2-3. references: Kulkarni, Steinlauf, and Hall, 1988, Genetics 118: 267-85. genetics: Deficient for diss. # Df(1)L271 origin: Induced by hybrid dysgenesis. discoverer: Sobels. references: Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. 1985, Genetics 111: 23-41. genetics: Deficient for fs(1)k10-kz. # Df(1)l-D7: see Df(1)D7 # Df(1)l-D34: see Df(1)D34 # Df(1)l(1)403: see Df(1)403 # Df(1)LB6 cytology: Df(1)19E4;20A2-3. origin: Induced by mitomycin-C. discoverer: Baldwin. references: Schalet and Lefevre, 1973, Chromosoma 73: 83-100. genetics: Deficient for shakB and -eo but not run. # Df(1)LB7 cytology: Df(1)19E4;? origin: Induced by mitomycin-C. references: Baird, Schalet, and Wyman, 1990, Genetics 126: 1045-59. Schalet (unpublished). genetics: Shows complete shakB phenotype over shakB1, but incomplete shakB phenotype over shakB2 or Df(1)16-3-35 (Baird et al.). Deficient for l(1)19Ec8-su(f). # Df(1)LB23 cytology: Df(1)19E6-7;20F. origin: Induced by ethyl methanesulfonate. discoverer: Baldwin. references: Schalet and Lefevre, 1973, Chromosoma 73: 83-100. genetics: Deficient for vao-su(f). #*In(1)lz: Inversion (1) lozenge origin: X ray induced. discoverer: Green and Green. references: 1956, Z. Indukt. Abstamm. Vererbungsl. 87: 708-21. genetics: Mutant for spectacled-like alleles of lz. inversion cytology ( ________________________ *In(1)lz1 8D;20F *In(1)lz2 8D;20F *In(1)lz3 4D;8D *In(1)lz4 8A2-B1;8D *In(1)lz5 8D;18F2-19A1 *In(1)lz6 8D;9B12-C1 *In(1)lz7 8D;20F ( Hannah. #*Df(1)lzA: see In(1)lzA # Df(1)m13 cytology: Df(1)10B8;11A3-5. references: Woods, and Bryant, 1989, Dev. Biol. 134: 222-25. genetics: Deficient for l(1)10Bg. # Df(1)m259-4: Deficiency (1) miniature cytology: Df(1)10C2-3;10E1-2 (Mortin and Lefevre, 1981, Chromo- soma 82: 237-47). origin: X ray induced. discoverer: Demerec, 33i. references: Dorn and Burdick, 1962, Genetics 47: 503-18. Craymer and Roy, 1980, DIS 55: 200-04. Greenleaf, Weeks, Voelker, Ohnishi, and Dickson, 1980, Cell 21: 785-92. Voelker, Wisely, Huang, and Gyurkovics, 1985, Mol. Gen. Genet. 201: 437-45. genetics: Male lethal. Heterozygote with m has m phenotype. Heterozygote with dy is wild type. Recombines with m59, m, mD, dy61a, dy, and dy58k. Includes tyl (Craymer and Roy, 1980) and RpII (Greenleaf et al., 1980). Df(1)m259-4/Df(1)KA6 survives and is extreme m (Craymer and Roy, 1980). molecular biology: Left DNA breakpoint between -19 and -23 kb (Woods and Marsh). # Df(1)m-fw: Df(1) miniature to furrowed references: Green, 1975, Mutat. Res. 29: 77-84. genetics: Deficient for m-fw. # Df(1)m-KA7: see Df(1)KA7 #*Df(1)M30: Deficiency (1) Minute-30. origin: Spontaneous. discoverer: Schultz. references: 1929, Genetics 14: 366-419. genetics: Deficient for cv and M(1)5D6A. # Df(1)M31 - Df(1)M176 origin: Induced by ethyl methanesulfonate. deficiency cytology ref ( genetics ______________________________________________________ Df(1)M31 {20A(prox)} 1 uncl--ms(1)B- Df(1)M54 2B10;2B18 2 Df(1)M82 {20A(prox)} 1 uncl- Df(1)M158 {20A(prox);20B-D} uncl--ms(1)A- Df(1)M171 {19E(distal)} run--ms(1)E- Df(1)M176 {19E(distal)} run--shakB- ( 1 = Lifschytz and Yakobovitz, 1978, Mol. Gen. Genet. 161: 275-84; 2 = Lim and Snyder, 1954, Genet. Res. 24: 1- 101. # Df(1)mal: Deficiency (1) maroonlike origin: X ray induced. deficiency cytology ref ( genetics _______________________________________________________________________ Df(1)mal {19A1-2;20E-F} 2 l(1)carot3+ ot--su(f)- bb+ + In(1)sc8 Df(1)mal3 19A1-2;20E-F 1, 5, 6 l(1)carot3+ ot--su(f)- bb+ Df(1)mal4 {19A1-2;20A2-3} 1, 5, 6 l(1)carot3+ ot--eo- wap+ Df(1)mal5 {19A-B;19E8-F1} 1, 5, 6 l(1)carot3+ sw--vao- unc+ Df(1)mal6 19C3;20A2-3 + 1, 5, 6 mel+ mal--eo- wap+ In(1)BM1 Df(1)mal7 {19A1-2;19F-20A1} 1, 5, 6 l(1)carot3+ ot--fliI- eo+ Df(1)mal8 18F4-5;19E1 1, 5, 6 l(1)carot3+ ot--mell- run+ Df(1)mal9 {19A1-2;20-E-F} + 1, 5 l(1)carot3+ ot--su(f)- bb+ In(1)sc8 Df(1)mal10 19A5-6;19E1 + 1, 3, 5, 6 ot+ sw--mell- run+; In(1)sc8 Df(1)mal10/sw females lethal; Df(1)mal10/Ubl shows moderate sw effect Df(1)mal11 19A2-3;19E1 + 1, 5, 6 l(1)carot3+ ot--mell- run+ In(1)sc8 Df(1)mal12 19A1;20F + 1, 4, 5, 6 l(1)carot3+ ot--su(f)- bb; In(1)sc8 covered by y+Ymal+. Df(1)mal12/bb females bb; Hw effect. Df(1)mal13 19A2-3;20E-F 1, 5, 6 mel+ mal--su(f)- bb+ Df(1)mal17 | 19A2-3;19E1 + 1, 5, 6 l(1)1Ac--ac-, bb; l(1)carot3+ In(1)scS1Lsc8R ot--mell- run+ (double deficiency) Df(1)mal22 19C3;19E1 1, 5, 6 mel+ mal--mell- run+ ( 1 = Chovnick, Finnerty, Schalet, and Duck, 1969, Genetics 62: 145-70; 2 = Grell, 1962, Z. Indukt. Abstamm. Verer- bungl. 93: 371-77; 3 = Mortin and Lefevre, 1981, Chromosoma 82: 237-47; 4 = Schalet, 1969, Genetics 63: 133-53; 5 = Schalet and Finnerty, 1968, DIS 43: 65-66; 6 = Schalet and Lefevre, 1976, The Genetics and Biology of Drosophila (Ashburner and Novitski, eds.). Academic Press, London, New York, San Francisco, Vol. 1b, pp. 846-902. | Effectively a terminal deletion. # Df(1)mm69: Deficiency (1) methyl methanesulfonate cytology: {Df(1)3A9;3B1}. origin: Induced by methyl methanesulfonate. synonym: l(1)m69. references: Liu and Lim, 1975, Genetics 79: 601-11. genetics: Deficient for l(1)3Ah-l(1)3Ba. # Df(1)mo cytology: Breaks in In(1)wm4h (distal region). origin: X ray induced. references: Reuter and Wolff, 1981, Mol. Gen. Genet. 182: 516-19. # Df(1)N: Deficiency (1) Notch deficiency cytology origin discoverer ref ( genetics molec biol | ________________________________________________________________________________________________________________________________ Df(1)N-8 3C2-3;3E3-4 spont Mohr 13, 21, 22, 28 N--l(1)3Ec- (Lefevre) *Df(1)N-25 spont Mohr 3 w+ N- *Df(1)N-26 3C4-5;3C8-9 spont Mohr 3 rst+ fa--spl- dm+ *Df(1)N-29 spont Eker 3 w--N- *Df(1)N-33h 3C6-7;3D2-3 spont Ives 24, 25 w+ fa- ec+ *Df(1)N-38g 3C4-5;3C7-8 spont Curry 3 rst+ fa--spl- dm+ Df(1)N-45e 3B4-C1;3C7-8 X ray Poulson 9, 26, 34 N- Df(1)N-54l9 / 3C5-6;3C10-11 spont 13, 16, 17 ,20 vt--N-; viable and vt over Df(1)w67k30 Df(1)N-62b1 3C7-8 (or 3C7);3D5-6 X ray Ives 10, 29, 31, 32, 33 N55e11+fag--dm- -19.3 to -18.6 kb Df(1)N-62G1 6 N-; covered by Dp(1;2)51b Df(1)N-63b 3C2-3;3E1-2 X ray 18 rst--dm-; carries w63b; Df(1)N-63b/w resembles wsp/w Df(1)N-64i16 3C3;3D4 Welshons 11, 12 rst--dnc-; males see ref 8 sterile with w+Y Df(1)N64j15 3C3-4;3D3-4 X ray Welshons 11, 19 rst--Sgs-4-; males see ref 5 fertile with w+Y Df(1)N-66h10 3C1-2;3C6-7 mutable w8 Green 1, 8, 31, 32, 33 w--N55e11-fag+ see ref 8 Df(1)N-66h12 8 see ref 8 Df(1)N-66h31 8 see ref 8 Df(1)N-66i25 3C1-2;3C6-7 mutable w8 Green 1, 7, 10, 31, 33 w--N264-40- NCo+ +0.8 to +2.7 kb Df(1)N-68f19 3C1-2;3C6-7 mutable w8 Green 7, 10, 31, 33 w--N55e11- N264-40+ -26.2 to -24.7 kb Df(1)N-69h9 3C6;3D1 (Korge); X ray Lefevre 4, 13, 19 N--Sgs-4- 3C6;3D4 (Lefevre) Df(1)N-71a 3A6;3C10 (Lefevre) X ray Lefevre 15 Df(1)N-71b9 3C2-3;3E3-4 X ray Lefevre 15 N- Df(1)N-71h 3C4;3D5 Green 2, 4, 5, 11, 12 N--dnc- see ref 5 Df(1)N-75j31 3C7-9;3C10-D1 unequal Welshons 1, 33 N55e11+fag--N60g11- see ref 8 crossover Df(1)N-81k1 3C5-6;3C9-10 X ray Muskavitch 8 N- -43.9 to -31.2 kb (Welshons) Df(1)N-81l4 3C5-6;3D4-5 X ray Muskavitch 1, 8 N- (Welshons) Df(1)N-81l6 ` 3C7-9;3D2-3 X ray Muskavitch 1, 8 rst+N55e11+fa--Nj24 -14.8 to -9.5 kb (Welshons) *Df(1)N-264-2 3C6-7;3C7-8 X ray Demerec 28 rst+ fa- spl- ec+ *Df(1)N-264-7 3C6-7;3C8-9 X ray Demerec 3 see *In(1)N264-7 *Df(1)N-264-13 3C6-7;3C10-11 X ray Demerec 3 rst+ fa- fan- spl- dm+ *Df(1)N-264-15 3C6-7;3C7-8 X ray Demerec 3 w+ fa- spl- *Df(1)N-264-19 3C6-7;3C7-8 X ray Demerec 28 w+ fa- ec+ *Df(1)N-264-30 3A4-5;3C7-9 X ray Demerec 27 kz+ w--fa- dm+ *Df(1)N-264-31 3B4-C1;3D1-3 X ray Demerec 27 pn+ w--dm- ec+ *Df(1)N-264-32 3C3-5;3C7-8 X ray Demerec 27 w+ rst--fa- dm+ *Df(1)N-264-33 3C6-7;3C7-8 X ray Hoover 27 rst+ fa- dm+ *Df(1)N-264-36 3A3-4;3D2-3 X ray Demerec 27 w--dm- *Df(1)N-264-37 3C6-7;3C7-8 X ray Demerec 27 rst+ fa- dm+ Df(1)N-264-38 2D3-4;3E2-3 X ray Demerec 27 br+ pn--dm- Df(1)N-264-39 - 3C6-7;3C7-8 spont Slizynska 28, 30 N- *Df(1)N-264-41 3C6-7;3C8-9 spont Slizynska 3 rst+ fa- dm+ *Df(1)N-264-42 3C4-5;4B4-6 X ray Demerec 3 rst+ fa--ec- bi+ *Df(1)N-264-46 3C6-7;3C7-8 X ray Demerec 3 rst+ fa- dm+ *Df(1)N-264-48 1B6-7;1B10-11 X ray Demerec 3 see *In(1)N264-48 *Df(1)N-264-49 3C4-5;3E8-F1 X ray Demerec 3 rst+ fa- ec+ *Df(1)N-264-51 3C6-7;3C7-8 radium? Demerec 3 rst+ fa- dm+ *Df(1)N-264-54 3C3-5;3C7-8 X ray Demerec 3 rst+ fa- dm+ Df(1)N-264-58 3B2-3;3D6-7 X ray Demerec 3 see Tp(1;3)N264-58 *Df(1)N-264-68 3A10-B1;3E8-F1 X ray Demerec 3 kz+ w- ec+ *Df(1)N-264-72 3C6-7;3C7-9 X ray Demerec 3 rst+ fa- dm+ *Df(1)N-264-73 3C3-4;4C6-7 X ray Demerec 3 w+ rst- bi+ *Df(1)N-264-76 3B4-C1;3E4-5 X ray Demerec 3 pn+ w- ec+ *Df(1)N-264-77 3B4-C1;3C7-8 X ray Demerec 3 pn+ w--dm- ec+ *Df(1)N-264-79 2C10-D1;3C6-7 X ray Demerec 3 br+ kz--rst- dm+; weak N; fa affected *Df(1)N-264-81 3C6-7;3C7-8 X ray Demerec 3 rst+ fa- dm+ *Df(1)N-264-86 3C7-8;3E5-6 X ray Demerec 3 see *Tp(1;4)N264-86 *Df(1)N-264-89 3B2-3;3F2-3 X ray Demerec 3 pn+ w--ec- *Df(1)N-264-90 3C7-8;3E8-F1 X ray Demerec 3 w+ spl--ec- *Df(1)N-264-93 3B4-C1;3F3-4 X ray Demerec 3 pn+ w--ec- bi+ *Df(1)N-264-96 3C6-7;3C7-8 X ray Demerec 3 rst+ spl- dm+ *Df(1)N-264-99 2D2-3;3C11-12 X ray Demerec 3 pn--dm- ec+ *Df(1)N-264-100 3B4-C1;4B4-5 X ray Demerec 3 see *T(1;3)N264-100 *Df(1)N-264-101 3C4-5;3C7-8 X ray Demerec 3 rst+ spl- dm+ Df(1)N-264-105 3C6-7;3D2-3 X ray Demerec 13 rst+ spl--Sgs-4- ec+ *Df(1)N-264-106 3C6-7;3C7-8 X ray Demerec 3 rst+ spl- dm+ *Df(1)N-264-108 3C3-5;3E7-8 3 see *In(1)N264-108 *Df(1)N-264-110 3B4-C1;3D2-3 X ray Demerec 3 pn+ w--dm- ec+ *Df(1)N-264-111 3C3-5;3C12-D1 X ray Demerec 3 w+ rst--spl- dm+ *Df(1)N-264-114 3C6-7;3D4-5 spont Kaufmann 3 w+ rst--dm- ec+ *Df(1)N-264-115 3C3-5;3E2-3 X ray Sutton 3 w+ rst--dm- *Df(1)N-264-117 3A6-7;3E2-3 X ray Demerec 3 pn+ w--dm- ec+ *Df(1)N-264-118 3C6-7;3C7-9 spont Demerec 3 rst+ spl- dm+ *Df(1)N-264-120 3C6-7;3D2-3 X ray Demerec 3 rst+ spl--dm- ec+ *Df(1)N-264-125 3C4-5;3C7-8 X ray Demerec 3 rst+ spl- dm+ *Df(1)N-264-126 3C3-5;3D4-5 spont Bishop 3 w+ rst--dm- *Df(1)N-264-127 3C6-7;3C7-8 X ray Demerec 3 rst+ spl- dm+ *Df(1)N-264-128 3C6-7;3C7-8 X ray Demerec 3 rst+ spl- dm+ *Df(1)N-264-130 3C6-7;3C7-8 spont Neel 23 rst+ fa- dm+ *Df(1)N-B 3C4-5;3C12-D1 spont Bernstein 3 rst+ fa- dm+ Df(1)N-cm n 3C7-8;3D3-5 unstable Lim 14 N- cm- see ref 14 chromosome *Df(1)N-EZ 3C6-7;3C7-8 spont Morgan 3 w+ fa- Df(1)N-FM21 3C1-2;3C7-D1 Bingham 19 w--Sgs-4- Df(1)N-h77.2 X ray on 27 w--dm-;bb- In(1)wm4 Df(1)N-M1 X ray on 27 w--dm-;bb- In(1)wm4 Df(1)N-M2 X ray on 25 w--dm-;bb- In(1)wm4 Df(1)N-M8 X ray on 25 w--dm-;bb- In(1)wm4 ( 1 = Artavanis-Tsakonas, Muskavitch, and Yedvobnick, 1983, Proc. Nat. Acad. Sci. USA 80: 1977-81; 2 = Byers, Davis, and Kiger, 1981, Nature 289: 79-81; 3 = CP627; 4 = Craymer and Roy, 1980, DIS 55: 200-04; 5 = Davis and Davidson, 1984, Mol. Cell Biol. 4: 358-67; 6 = Doane, 1969, J. Exp. Zool. 171: 321-42; 7 = Green, 1967, Genetics 56: 467-82; 8 = Grimwade, Muskavitch, Welshons, Yedvobnick, and Artavanis-Tsakonas, 1985, Dev. Biol. 107: 503-19; 9 = Hill- man, 1961, Genetics 46: 1395-1409; 10 = Kidd, Lockart, and Young, 1983, Cell 34: 421-33; 11 = Kiger and Golanty, 1977, Genetics 85: 609-22; 12 = Kiger and Golanty, 1979, Genetics 91: 521-35; 13 = Korge, 1977, Chromosoma 62: 155-74; 14 = Johnson-Schlitz and Lim, 1987, Genetics 115: 701-09; 15 = Lefevre; 16 = Lefevre, 1971, DIS 46: 40; 17 = Lefevre and Green, 1972, Chromosoma 36: 391-412; 18 = Lefevre and Wilkins, 1966, Genetics 53: 175-87; 19 = McGinnis, Far- rell, and Beckendorf, 1980, Proc. Nat. Acad. Sci. USA 77: 7367-71; 20 = Mohler, 1956, DIS 30: 78; 21 = Mohr, 1919, Genetics 4: 275-82; 22 = Mohr, 1932, Proc. Int. Congr. Genet., 6th, pp. 202; 23 = Neel, 1942, Genetics 27: 530; 24 = Plough and Ives, 1934, DIS 1: 31; 25 = Plough and Ives, 1934, DIS 2: 10,34; 26 = Poulson, 1945, DIS 19: 47; 27 = Reuter, Hoffmann, and Wolff, 1983, Biol. Zentralbl. 102: 281-98; 28 = Slizynska, 1938, Genet- ics 23: 291-99; 29 = Sorsa and Saura, 1980, Hereditas 92: 341-51; 30 = Welshons, 1958, Proc. Nat. Acad. Sci. USA 44: 254-58; 31 = Welshons, 1974, Genetics 76: 775-94; 32 = Welshons and Keppy, 1975, Genetics 80: 143-55; 33 = Welshons and Keppy, 1981, Mol. Gen. Genet. 181: 319- 24; 34 = Wright, 1970, Adv. Genet. 15: 262-85. | The zero coordinate used in locating the molecular lesions in the Notch deficiencies is the first Eco R1 site in Canton-S DNA proximal to the 3C7 breakpoint of In(1)N76b8 (Kidd et al., 1983); it is 1.1 kb to the right of the zero coordinate used by Artavanis-Tsakonis et al., 1983. / Lacks Sgs-4 sequences (McGinnis et al., 1980). ` 3C7 not deleted but appears thinner than normal (Grimwade et al., 1985). - Later reexamination of chromosomes of males from lines car- rying wch and marked N264-39 revealed the presence of 3C7 (Welshons). Cell lethal and lethal in germ-line clones (Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53). n 50 Notch mutations originating independently in In(1)cm-df = In(1)3D;6D + Df(1)6D;6F (a derivative of the unstable X Uc- 1lJD15) showed this apparently identical X chromosome defi- ciency (New order: 1A1 - 3C7 | 6D - 3D | 6F - 20). Results from in situ hybridizations with 20 of these deficiencies indicated a deletion of 10 kb of the sequences from the 3' end of Notch had occurred (Johnson-Schlitz and Lim, 1987). The break position of these Notch deficiencies is within the 2.2 kb Eco R1 fragment with the next 3'-most clone (Kidd et al., 1983), which corresponds to the region between N264-40 and spl in the genetic map. # Df(1)N12-Df(1)N110 origin: X ray induced. discoverer: Lefevre. deficiency cytology ref ( genetics ___________________________________________________________________________ Df(1)N12 | 11D1-2;11F1-2 1, 2, 3, 4, 5, 6, 8 sno--wy- s+ Df(1)N19 17A1;18A2 1, 2, 3, 8 os+ fu- hld- Df(1)N37 / 9B5-6;9D1-2 3 Hk+ flw- ras+ Df(1)N71 10B5;10D4 1, 3, 8, 9, 10 l(1)10Ag+ dsh--tyl- dy+ 10B2-8;10D3-8 (Zhimulev) Df(1)N73 5C2;5D5-6 1, 3, 7, 8 cv+ rux- l(1)5CDa- vs+ Df(1)N77 19E2-3;20E 3 mell--su(f)- Df(1)N105 10F7;11D1 1, 2, 3, 8 Flu- fw- Df(1)N110 / 9B3-4;9D1-2 1, 2, 3, 8 Hk- flw- ras+ ( 1 = Craymer and Roy, 1980, DIS 55: 200-04; 2 = Deak, Bel- lamy, Bienz, Dubuis, Fenner, Gollin, Rahmi, Ramp, Reinhardt, and Cotton, 1982, J. Embryol. Exp. Morphol. 69: 61-81; 3 = Lefevre; 4 = Lefevre and Peterson, 1972, DIS 48: 126- 27; 5 = Lefevre and Wright, 1976, Genetics 83: s44-45; 6 = Mortin and Lefevre, 1981, Chromosoma 82: 237-47; 7 = Voelker and Wisely, 1982, DIS 58: 150-51; 8 = Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307. 9 = Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Khudyakov, Patzevich, Semeshin, Baritcheva, Aizenzon, Kramers, and Eeken, 1982, DIS 58: 210-14; 10 = Zhimulev, Pokholkova, Bgatov, Semeshin, and Belyaeva, 1981, Chromosoma 82: 25-40. | Synonym: Df(1)sno-N12. / Listed incorrectly as vermilion deficiency by Kaplan and Trout, 1974, Genetics 77: 721-39. # Df(1)N-r69h9: see Df(1)N-69h9 # Df(1)NF2 cytology: Df(1)3C6-7;3E8. origin: X ray induced. discoverer: Lefevre. genetics: Deficient for N - slc. # Df(1)O4: see Tp(1;3)O4 # Df(1)ovo: Deficiency (1) ovo deficiency cytology ref ( genetics ___________________________________________________ Df(1)ovo4 2 ovo--rg- Df(1)ovo6 | 4C5-6;4E2-3 1 peb--rg- Df(1)ovo7 / 4C5-6;4E2-3 1 omb--rg- Df(1)ovo14 2 ovo--rg- Df(1)ovo15 2 ec--fs(1)A1621- Df(1)ovo41 2 rb--fs(1)A1621- Df(1)ovo44 2 bi--fs(1)A1621- ( 1 = Oliver, Perrimon, and Mahowald, 1988, Genetics 120: 159-71; 2 = Steinmann-Zwicki, 1988, EMBO J. 7: 3889-98. | Synonym: Df(1)ovo-D1rG6. / Synonym: Df(1)ovo-D1rG7. # Df(1)para: see Df(1)80-Df(1)82 # Df(1)PC1 origin: Induced by hybrid dysgenesis. references: Zusman, Coulter, and Gergen, 1985, DIS 61: 217-18. genetics: Complements uncl and l(1)20Cb but not fog or stn. # Df(1)Pgd35: Deficiency (1) Phosphogluconate dehydrogenase cytology: Df(1)2C2-4;2E2-F1 (Nero); Df(1)2D3;2F5 (Craymer and Roy, 1980). Perrimon et al. (1980) believe deficiency listed by Craymer and Roy is Df(1)Pgd-kz. references: Craymer and Roy, 1980, DIS 55: 200-204. Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. genetics: Deficient for Pgd and pn but not for l(1)2Ea. Viable and fertile over Df(1)X12. # Df(1)Pgd-kz: Deficiency (1) Phosphogluconate dehydrogenase to kurz cytology: Df(1)2D3-4;2F5. Bands faint. 2F6 preserved. origin: Co60 irradiation of PgdB Canton-S flies. references: Gerasimova and Ananiev, 1972, DIS 48: 93. Gvozdev, Gostimsky, Gerasimova, Dubrovskaya, and Braslovskaya, 1975, Mol. Gen. Genet. 141: 269-75. Gvozdev, Gerasimova, Kovalev, Ananiev, 1977, DIS 52: 67-68. Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. genetics: Deficient for Pgd-kz-l(1)2Fd but not for br. # Df(1)pn: Deficiency (1) prune origin: X ray induced. genetics: Deficient for pn. # In(1)pn: Inversion (1) prune origin: X ray induced. references: Ilyina, Sorokin, Belyaeva, and Zhimulev, 1980, DIS 55: 205. genetics: Mutant for pn. inversion cytology ___________________________ In(1)pn1 see Tp(1;2)pn1 In(1)pn36 see Tp(3;1)pn36 In(1)pn45 2D1-2;20A # Df(1)pn-ec: see *Tp(1;2)w+62g # Df(1)Q38 origin: Induced by ethyl methanesulfonate. references: Lifschytz and Falk, Mutat. Res. 8: 147-55. genetics: Presumed double lethal. # Df(1)Q219 origin: Induced by ethyl methanesulfonate. references: Lifschytz and Falk, Mutat. Res. 8: 147-55. # Df(1)Q408 origin: Induced by ethyl methanesulfonate. references: Lifschytz and Falk, 1969, Mutat. Res. 8: 147-55. # Df(1)Q539 cytology: Df(1)19E6;19F6-20A1. origin: Induced by ethyl methanesulfonate. references: Lifschytz and Falk, 1969, Mutat. Res. 8: 147-55. Schalet and Lefevre, 1973, Chromosoma 44: 183-200. Craymer and Roy, 1980, DIS 55: 200-04. genetics: Deficient for vao-l(1)19Ff. # Df(1)r: Deficiency (1) rudimentary deficiency cytology origin syn ( ref | genetics / _________________________________________________________________________ Df(1)r-D1 ` 14D1-2;15D1-2 ICR-170 1 2, 3, 4, 5 para- r- Df(1)r-D17 - 14F6;15A6 X ray 2 1, 3, 5 sbl-- r- Df(1)r-l9 ` 14D1;15D1 ICR-170 5 r- ( 1 = Df(1)(D); 2 = Df(1)D17; | 1 = Falk, McCaughin, and Cogley, 1977, Genetics 86: 765-77; 2 = Ganetzky, 1984, Genetics 108: 897-911; 3 = Jarry, 1979, Mol. Gen. Genet. 172: 199-202; 4 = Mason, Green, Shaw, and Boyd, 1981, Mutat. Res. 81: 329-43; 5 = Naguib and Jarry, 1981, Genet. Res. 37: 199-207; / Two Minutes surround r ; the one on the left, M(1)14C, is new, the one on the right is M(1)15D (Lefevre). ` Semilethal opposite r, r29, or r38. - Discoverer = M.M. Green. Proximal break is determined to be 14C-D by Lilly and Carl- son as opposed to Lefevre's determination of 14F6. # Df(1)r75c: see Tp(1;2)r+75c #*Dp(1;f)R1-*Dp(1;f)R43 origin: X-ray-induced-deletion of most of euchromatin from R(1)2. discoverer: Pontecorvo. synonym: Del(Xc2)1-Del(Xc2)43. duplication cytology new order ref ( _________________________________________________________________ *Dp(1;f)R1 | 1 *Dp(1;f)R35 1A3-4;17A4-5; |17A5 - 20.20F| 2 19F-20A1 *Dp(1;f)R36 1A3-4;17A4-5; |17A5 - 20.20F| 2 19F-20A1 *Dp(1;f)R37 1A3-4;16F2-3; |16F3 - 20.20F| 2 19F-20A1 *Dp(1;f)R38 1A3-4;1F;20 |1A4 - 1F|20.20F - 20A1| 1 *Dp(1;f)R40 1A3-4;1F4-5;20 |1A4 - 1F4|20.20F - 20A1| 2 *Dp(1;f)R41 1A3-4;1F4-5;20 |1A4 - 1F4|20.20F - 20A1| 2 *Dp(1;f)R42 1A3-4;2A2-3;20 |1A4 - 2A2|20.20F - 20A1| 2 *Dp(1;f)R43 1A3-4;1F4-5;20 |1A4 - 1F4|20.20F - 20A1| 2 ( 1 = Pontecorvo, 1942, DIS 16: 65; 2 = Slizynska, 1942, DIS 16: 67. | Deletion of most of X euchromatin. # Df(1)R-9-1 origin: Induced by ethyl methanesulfonate. references: Lifschytz and Falk, 1969, Mutat. Res. 8: 147-55. # Df(1)R-10-5 origin: Induced by ethyl methanesulfonate. references: Lifschytz and Falk, 1969, Mutat. Res. 8: 147-55. # Df(1)RA origin: X ray induced. discoverer: Lefevre. deficiency cytology ref ( genetics ______________________________________________________________________________ Df(1)RA2 | 7D10;8A4-5 3, 4, 5, 6, 7 sdt--ptg- / Df(1)RA19 1E3-4;2B9-10 1, 2, 3 l(1)1EFa--fmf- Df(1)RA37 10A6;10B15-17 3, 5, 7, 8, 9, 10 l(1)10Ac+ l(1)10Ad--dsh- tyl+ Df(1)RA47 10F1;10F9-10 3, 5, 7 dy+ ftd- fw+ ( 1 = Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kra- mers, and Zhimulev, 1982, DIS 58: 184-90; 2 = Belyaeva, Aizenzon, Semeshin, Kiss, Koczka, Baritcheva, Gorelova, and Zhimulev, 1980, Chromosoma 81: 281-306; 3 = Craymer and Roy, 1980, DIS 55: 200-04; 4 = Gans, Forquignon, and Mas- son, 1980, Genetics 96: 887-902; 5 = Lefevre; 6 = Mortin and Lefevre, 1981, Chromosoma 82: 237-47; 7 = Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307; 8 = Zhimulev, Belyaeva, Pokhol- kova, Kochneva, Fomina, Bgatov, Khudyakov, Patzevich, Semeshin, Baritcheva, Aizenzon, Kramers, and Eeken, 1982, DIS 58: 210-14; 9 = Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 9-23; 10 = Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 25-40. | Synonym: Df(1)oc-RA2. / Df(1)RA2/Ubl females slight oc. # Df(1)ras: Deficiency (1) raspberry deficiency cytology discoverer ref ( genetics ___________________________________________________________________ Df(1)ras59 9E1;9F10-11 Nash 1 ras- Df(1)ras203 9E1-2;9F13 Nash 1, 2 ras- Df(1)ras217 9A;9E7-8 Nash 1 ras- Df(1)ras-P14 | 9E1-2;9F3-4 Patzevich 3, 4, 5 ras--l(1)9Fa- ( 1 = Janca, Woloshyn, and Nash, 1986, Genetics 112: 43-64; 2 = Nash and Janca, 1983, Genetics 105: 957-68; 3 = Zhimu- lev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Khu- dyakov, Patzevich, Semeshin, Baritcheva, Aizenzon, Kramers, and Eeken, 1982, DIS 58: 210-14; 4 = Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 9-23; 5 = Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 25-40. | origin: X ray induced. # Df(1)ras-v17: Deficiency (1) raspberry to vermilion cytology: Df(1)9D1-2;10A2-3 superimposed on In(1)1B3- 4;20FL1B2-3;20FR + In(1)4D7-E1;11F2-4. new order: 1A - 1B3|20F - 11F4|4E1 - 9D1|10A3- 11F2|4D7 - 1B4|20F. origin: X ray induced in In(1)scS1Lsc8R In(1)dl-49. synonym: Df(1)ras-v17Cc.8. references: Valencia, 1966, DIS 41: 58. Johnson, Woloshyn, and Nash, 1979, Mol. Gen. Genet. 174: 287-92. Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 9-23. genetics: Deficient for ras-sev. molecular biology: 10A2-3 breakpoint mapped to a restriction fragment between + 3.4 and 4.5 kb (Hafen, Basler, Ekstrom and Rubin, 1987, Science 36: 55-63); see molecular biology under sev for coordinates. # Df(1)ras-v-P26 cytology: Df(1)9C5-6;10A1. origin: X ray induced. discoverer: Zhimulev. genetics: Deficient for ras-csk. # Df(1)rb: Deficiency (1) ruby deficiency cytology origin ref ( genetics ___________________________________________________________ Df(1)rb1 3F6-4A1;4C7-8 / ray 1 mei-9--amb- Df(1)rb5 / ray 1 omb--rb- Df(1)rb12 3E3-5;4D3-7 / ray 1 mei-9--amb- Df(1)rb13 4C5-6;4D3-E1 / ray 1 lac--hnt- Df(1)rb13a 2 rb--fl(1)302- Df(1)rb14 2 rb--rg- Df(1)rb17 3E3-5;4F1-2 / ray 1 mei-9--amb- Df(1)rb19 3C7-9;4E3-F1 / ray 1 mei-9--amb- Df(1)rb23 2 ec--peb- Df(1)rb27 3C9-12;4D3-7 / ray 1 mei-9--amb- Df(1)rb27a 2 bi--rb- Df(1)rb29 2 bi--fl(1)302- Df(1)rb30 4B1-2;4F2-4 / ray 1 mei-9--Sxl- Df(1)rb32 4A6-B2;4E2-F1 / ray 1 mei-9--svb- Df(1)rb33 3F3-4;4C15-16 / ray 1 mei-9--hnt- Df(1)rb34 2 bi--peb- Df(1)rb35 2 bi--fl(1)302- Df(1)rb41 4B6-C1;4C7-8 / ray 1 mei-9--amb- Df(1)rb42 4B;4C 2 bi--rb- Df(1)rb44 2 bi--rb- Df(1)rb46 4A3-6;4C6-7 / ray 1 norpA--amb- Df(1)rb47 4A1-2;4D1-2 / ray 1 cho--hnt- Df(1)rb48 2 bi--fl(1)302- Df(1)rb50 2 bi--rb- Df(1)rb-V 4B4-5;4D5-6 X ray 3 rb- ( 1 = Banga, Bloomquist, Brodberg, Pye, Larrivee, Mason, Boyd, and Pak, 1986, Chromosoma 93: 341-46; 2 = Steinmann-Zwicki, 1988, EMBO J. 7: 3889-98; 3 = Valencia, 1966, DIS 41: 58. # Df(1)RC29 cytology: Df(1)11A. discoverer: Lefevre. genetics: cac-fw. # Df(1)RC40 cytology: Df(1)4B1;4F1. origin: X ray induced. discoverer: Lefevre. synonym: Df(1)biRC40. references: Craymer and Roy, 1980, DIS 55: 400-04. Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux Arch. Dev. Biol. 193: 296-307. Bausenwein, Wolf, and Heisenberg, 1986, J. Neurogenet. 3: 87-109. Bottella, Grond, Saiga, and Edstrom, 1988, EMBO J. 7: 3881- 88. genetics: Deficient for bi, rb, rg and svb but not ec, cho, bo, or cx. Df(1)RC40/Ubl females show slight bi phenotype (Mortin and Lefevre, 1981, Chromosoma 82: 237-47). Df(1)RC40/In(1)ombH31 females show ombH31 phenotype (Heisen- berg). # Df(1)RF19 cytology: Df(1)7A4-5;7B2-3 + In(1)6A1;19E8. origin: X ray induced. discoverer: Lefevre. references: Johnson and Judd, 1979, Genetics 92: 485-502. Nicklas and Cline, 1983, Genetics 103: 617-31. Lefevre and Leeds, 1983, Genetics 104: s45-46. genetics: Homozygous lethal. Deficient for l(1)7Ab--kf-. Com- pletely complements ctn, ct6, and ctK; fails to complement kf2. In(1)HA46/Df(1)RF19 flies show kf2 phenotype (Lefevre and Leeds, 1983). molecular biology: Proximal breakpoint 55.2 - 50.5 kb distal to the insertion site of gypsy in ct6 (Jack, 1985, Cell 42: 869-76). # Df(1)RF19 - Df(1)RF55 origin: X ray induced. discoverer: Lefevre. deficiency cytology genetics _____________________________________________ Df(1)RF19 see separate entry Df(1)RF21 19E2;20E-F run--su(f)- Df(1)RF39 1A1;1B10-11 l(1)1Aa--vnd- Df(1)RF44 1A1;1A6-7 l(1)1Aa--l(1)1Ac- Df(1)RF55 19A;20 # Df(1)RK references: B. Ganetzky. deficiency cytology origin genetics ______________________________________________________________ Df(1)RK2 12D2-E1;13A2-5 / ray ben- eag- na- Df(1)RK3 12E2-6;13A6-11 / ray eag- Df(1)RK4 12F5-6;13A9-B1 recombination ( eag- Df(1)RK5 12E9-11;13A9-B1 recombination | eag- ( Between In(1)N282.2 and In(1)P363 (W.R. Engels). | Between In(1)N282.2 and In(1)N366.2 (W.R. Engels). # Df(1)RpII215-61 cytology: Df(1)10B8-9;10E1-2. origin: Induced by hybrid dysgenesis. references: Voelker, Wisely, Huang, and Gyurkovics, 1985, Mol. Gen. Genet. 201: 437-45. genetics: Deficient for RpII215. # Df(1)RpII215-172 cytology: Df(1)10A1-2;11A1-2. origin: Induced by hybrid dysgenesis. references: Voelker, Wisely, Huang, and Gyurkovics, 1985, Mol. Gen. Genet. 201: 437-45. genetics: Deficient for RpII215. # Df(1)rst2: Deficiency (1) roughest cytology: Df(1)3C3-4;3C6-7. origin: Spontaneous. discoverer: Bridges, 33d7. references: Gruneberg, 1937, J. Genet. 34: 169-89. Emmets, 1937, J. Genet. 34: 191-202. Gersh, 1965, Genetics 51: 477-80 (fig.). Gubb, Roote, Harrington, McGill, Durrant, Shelton, and Ash- burner, 1985, Chromosoma 92: 116-23. genetics: Deficient for rst and vt. Hemizygous males and homozygous females viable; emergence delayed (Lefevre and Green, 1972, Chromosoma 36: 391-412). # Df(1)run1112: Deficiency (1) runt cytology: Df(1)19D-E. origin: Induced by ethyl methanesulfonate. references: Gergen and Wieschaus, 1986, Cell 45: 289-99. Gergen, 1987, Genetics 117: 477-85. genetics: Deficient for mal, run, vao. # Df(1)S39 cytology: Df(1)1E1;2B5-6 (Lefevre). Df(1)1E1-2;2B5-6 (Belyaeva et al., 1982) or Df(1)1E3;2B9 + In(1)1D1-2;1E1 (Lefevre). origin: X ray induced. discoverer: Lefevre. synonym: Df(1)brS39. references: Craymer and Roy, 1980, DIS 55: 200-04. Mortin and Lefevre, 1981, Chromosoma 82: 237-47. Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kramers, and Zhimulev, 1982, DIS 58: 184-90. Kramers, Schalet, Paradi, and Huiser-Hoogteyling, 1983, Mutat. Res. 107: 187-201. genetics: Deficient for l(1)1Ea - l(1)2Bd but not for dor. Inversion produces a su(wa) effect (Lefevre). Df(1)S39/+ females slight br, Df(1)S39/br females lethal (Lefevre). molecular biology: 2B5-6 breakpoint between DNA coordinates 217 and 220.8 kb (Chao and Guild, 1986, EMBO J. 5: 143-50). # Df(1)S54 cytology: Df(1)19E8;20A2. origin: X ray induced. discoverer: Lefevre. references: Perrimon, Smouse, and Miklos, 1989, Genetics 121: 313-31. genetics: unc--eo-. # Df(1)s70e cytology: Df(1)4D1-2;4D7 (light bands missing). origin: Induced by mutator gene, mu. references: Green and Lefevre, 1972, Mutat. Res. 16: 59-64. # Df(1)S93: see Tp(1;1)S93 # Df(1)SBLA cytology: Df(1)17A;17B (Beermann). origin: X ray induced. references: Lifschytz and Green, 1979, Mol. Gen. Genet. 171: 153-59. genetics: Male lethal. Uncovers hdp-a5; Bx3/Df(1)SBLA has nor- mal wing phenotype. # Df(1)sbr: Deficiency (1) small bristle origin: X ray induced. discoverer: Kochneva. references: Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 9-23. Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Khu- dyakov, Patzevich, Semeshin, Baritcheva, Aizenzon, Kramers, and Eeken, 1982, DIS 58: 210-14. deficiency cytology genetics ______________________________________________ Df(1)sbr1 9B9-10;9F13-10A1 ras--l(1)9Fg- Df(1)sbr8 9B1-2;10A1-2 ras--l(1)10Aa- Df(1)sbr9 9A2-4;10A1-2 ras--l(1)10Aa- Df(1)sbr10 9A2-4;9F13-10A1 ras--l(1)9Fg- # Df(1)sc4Lsc8R: see In(1)sc4Lsc8R # Df(1)sc4LscL8R: see In(1)sc4LscL8R # Df(1)sc8: Deficiency (1) scute-8 cytology: Df(1)1A1;1B2. origin: Spontaneous in In(1)sc8. discoverer: Noujdin. references: 1935, Zool. Zh. 14: 317-52. Baker, 1973, Dev. Biol. 33: 429-40. Deak, I.I., Bellamy, Bienz, Dubuis, Fenner, Gollin, Rahmi, Ramp, Reinhardt, and Cotton, 1982, J. Embryol. Exp. Morphol. 69: 61-81. genetics: Deficient for cin, l(1)1Ac, y, ac, Hw, and ewg (Deak et al., 1982). Male lethal, dies as late embryo; larva nearly complete (Poulson, 1940, J. Expt. Zool. 83: 271-325) but little or no muscular movement (Wright, 1970, Advances in Genetics 15: 262-85). #*Df(1)sc825b - *Df(1)sc8WO A series of derivatives of either In(1)sc8 or In(1)sc8LENR that have lost spontaneously the distal euchromatic segment of In(1)sc8, with or without the loss of adjacent X heterochroma- tin. The material lost may be replaced with YS by means of exchange between YS and the heterochromatic segment of the X removed distally by In(1)sc8; alternatively, the X terminus may not be capped by a recognizable element. The material lost is required for viability; this requirement can be met by either In(1)ENR or y+Y. discoverer: Lindsley (except for Df(1)sc8-M which was discovered by Mather, 1937). synonym: sc8c.o.X [In(1)sc8 derivatives] or sc8ENc.o.X [In(1)sc8LENR derivatives]. deficiency ref ( genetics _______________________________________ *Df(1)sc825b |` 2 y- ac- bb *Df(1)sc835a / 1 KS y--ac- bb+ *Df(1)sc853c / 2 y- ac- *Df(1)sc867h | 1 KS y- ac- bb+ *Df(1)sc889a | 1 KS y--ac- bb+ *Df(1)sc891b | 1 KS y- ac- bb+ *Df(1)sc899c | 2 y- ac- bb+ *Df(1)sc8B1 /` 2 y- ac- *Df(1)sc8C4 / 2 y- ac- *Df(1)sc8C6 /` 2 y- ac- *Df(1)sc8C13 / 2 y- ac- *Df(1)sc8D6 / 2 y- ac- *Df(1)sc8D8 /` 2 y- ac- *Df(1)sc8E1 | 1 KS y- ac- bb+ *Df(1)sc8F7 / 2 y- ac- *Df(1)sc8J3 /` 2 y- ac- bb *Df(1)sc8K1 /` 2 y- ac- bb *Df(1)sc8L7 / 1 KS y- ac- bb+ *Df(1)sc8M | *Df(1)sc8O7 / 2 y- ac- *Df(1)sc8P0 | 1 KS y- ac- bb+ *Df(1)sc8P0 / 1 KS y- ac- bb+ Df(1)sc8P7 / 1 KS y- ac- bb+ *Df(1)sc8Q1 /- 2 y- ac- *Df(1)sc8S7 /` 2 y- ac- bb- *Df(1)sc8W0 /` 2 y- ac- bb- ( 1 = Lindsley, 1955, Genetics 40: 24-44. 2 = Lindsley, 1958, Z. Indukt. Abstamm. Vererbungsl. 89: 103-22. | Spontaneous derivative of In(1)sc8. / Spontaneous derivative of In(1)sc8LENR. ` Lacks hB and the portion of hA distal to the right break- point of In(1)sc8. - Lacks the portion of hA distal to the right breakpoint of In(1)sc8. # Df(1)sc8Lsc4R: see In(1)sc8Lsc4R # Df(1)sc8LscL8R: see In(1)sc8LscL8R # Df(1)sc8LscS1R: see In(1)sc8LscS1R # Df(1)sc260-25: see In(1LR)sc260-25 # Df(1)scL8Lsc8R: see In(1)scL8Lsc8R # Df(1)scL8LscS1R: see In(1)scL8LscS1R # Df(1)scV1: see In(1LR)scV1 # Df(1)sc10-1 cytology: Df(1)1B1-2;1B2-3. new order: 1A - 1B1|1B14 - 1B3|1C1 - 20; 1B2 missing. origin: X-ray-induced derivative of In(1)ac3 = In(1)1B2- 3;1B14-C1. discoverer: Sturtevant, 1930. references: 1935, DIS 3: 15. 1936, Genetics 21: 444-66. Garcia-Bellido, 1979, Genetics 91: 491-520. Villares and Cabrera, 1987, Cell 50: 415-24. genetics: Mutant for ac and sc; male viability low. The adults, which occasionally eclose, lack macro- and microchae- tae, except those of the eye and wing margin. Homozygous cell clones in wing lack neurons except along anterior margin (Schubiger and Palka, 1985, Dev. Biol. 108: 399-410). molecular biology: No deletion detected in cloned ac region (Campuzano, Carramolino, Cabrera, Ru'z-G'mez, Villares, Boronat, and Modolell, 1985, Cell 40: 327-38). Sequence data indicate that there is a C to T change in nucleotide 669, a C to G change in nucleotide 1143 that converts Ser 101 to Arg, and a C to T change in nucleotide 1147 that generates a stop codon (Villares and Cabrera, 1987). #*Df(1)sc15 origin: X ray induced. discoverer: Muller. references: Patterson and Muller, 1930, Genetics 15: 495-577. Dubinin, 1933, J. Genet. 27: 443-64. genetics: Mutant for sc; deficient for y and ac. Apparently, y+ and ac+ loci were inserted into an autosome and subse- quently lost. Originally tested as an allele of sc only. Male lethal. # Df(1)sc19: see Tp(1;2)sc19 # Df(1)sc-B57 references: Gonzalez, Romani, Cubas, Modolell, and Campuzano, 1989, EMBO J. 8: 3553-62. genetics: Deficient for ASC and l(1)1Bb. molecular biology: Shown to have left breakpoint between y and ac and right breakpoint just to the right of that of Df(1)260-1. # Df(1)sc-Fah: Deficiency (1) scute of Fahmy cytology: Df(1)1A8-B1;1B2-3. origin: Induced by DL-p-N,N-di-(2-chloroethyl) aminophenylalan- ine (CB. 3007). discoverer: Fahmy, 1954. references: 1958, DIS 32: 74. genetics: Probably mutant for sc. Male viable; homozygous female lethal. # Df(1)sc-J4: see T(1;3)scJ4 # Df(1)sd72b: Df (1) scalloped cytology: Df(1)13F1;14B1. origin: X ray induced. discoverer: Lefevre, 72b26. synonym: Df(1)sd. references: Craymer and Roy, 1980, DIS 55: 200-04. Ganetzky and Wu, 1982, Genetics 100: 597-614. Mortin and Lefevre, 1981, Chromosoma 82: 237-47. genetics: Deficient for sd but not for bas. Extreme sd phenotype over RpII215Ubl. # In(1)Si: Inversion (1) Simmons origin: Selected as sex-linked recessive lethals from P-M dys- genic crosses. references: Simmons, Raymond, Culbert, and Laverty, 1984, Genetics 107: 49-63. location of inversion cytology lethal ( __________________________________________ In(1)Si1 2B;14D1-2;19D1-2 14B13-15A9 In(1)Si2 11A2-6;14D1-2 19A1-20E In(1)Si3 14C7-D1;19C2-D1 14B13-15A9 In(1)Si4 14C7-D1;19C2-D1 14B13-15A9 In(1)Si5 14C8-D2;19C2-6 In(1)Si6 14D;19C 14B13-15A9 In(1)Si7 14D;19C 14B13-15A9 In(1)Si8 14D;19C 14B13-15A9 In(1)Si9 14D1-2;19A-D 14B13-15A9 In(1)Si10 14D1-2;19C2-5 14B13-15A9 In(1)Si11 14D1-2;19C-E 14B13-15A9 In(1)Si12 14D2-3;19C 14B13-15A9 In(1)Si13 14D2-E1;18F2-5 19A1-20E ( Determined by deficiency testing against Df(1)r75c = Df(1)14B13;15A9 and Df(1)mal3 = Df(1)19A1-2;20E-F. # Df(1)SJ1 origin: Spontaneous. discoverer: Schalet. deficiency genetics ___________________________________ Df(1)SJ1a l(1)1Aa--ewg- arth+ Df(1)SJ1b l(1)1Aa--l(1)1Ac- dmd+ Df(1)SJ1c l(1)1Aa--l(1)1Ac- dmd+ Df(1)SJ1d l(1)1Aa--l(1)1Ac- dmd+ # Df(1)slc-A113: see Df(1)A113 # DF(1)SMG # Df(1)SMG54: Deficiency (1) Semenova Mglinetz Glotoff cytology: Df(1)1C;1F. origin: / ray induced. synonym: Df(1)1C;1F. references: Semenova, Mglinetz, and Glotoff, 1970, Genetika (Moscow) 6: 165-69. # Df(1)sn: Deficiency (1) singed cytology: {Df(1)7C-D1;7D22-E1}. Distal breakpoint (7B2-3) of Hinton and Welshons, 1955, moved proximally since not defi- cient for ct. origin: Spontaneous in R(1)2. discoverer: C. Hinton. references: Hinton and Welshons, 1955, DIS 29: 125-26. genetics: Deficient for sn but not ct, oc, or ptg. # Df(1)sn-C128: see Df(1)C128 # Df(1)sno-N12: see Df(1)N12 # Df(1)sol: Deficiency (1) small optic lobes cytology: Small deficiency on X. references: Miklos, Kelly, Coombe, Leeds, and Lefevre, 1987, J. Neurogenet. 4: 1-19. genetics: Recessive lethal. Deficient for sol and four lethals, one to the left and three to the right. # Df(1)Sp: Deficiency (1) Spontaneous origin: Spontaneous in Amherst laboratory wild-type males, with the exception of Df(1)Sp(J1.d) and Df(1)Sp(ras-v). discoverer: Schalet. deficiency cytology synonym genetics _________________________________________________________________________ Df(1)Sp2F-3A 2F2;3A6 ( l(1)11-83 kz+ l(1)2Fb--l(1)3Ac- l(1)3Ad+ Df(1)Sp8A 7F10-8A1;8A2-3 l(1)7-107 gg+ l(1)8Aa--l(1)8Ab- oc+ Df(1)Sp20A-F 20A3;20F4 l(1)19-117 eo+ wap--su(f)- bb+ Df(1)Sp(br-dor) |/ l(1)19-30P sta+ br--dor- Df(1)Sp(J1a) l(1)1-96 l(1)1Ab--ewg- arth+ Df(1)Sp(J1b) l(1)5-13 l(1)1Ab--dmd- l(1)1Aa+ Df(1)Sp(J1c) l(1)17-18 l(1)1Ab--dmd- l(1)1Aa+ Df(1)Sp(J1d) / l(1)05-22 l(1)1Aa--l(1)1Ab- cin+ Df(1)Sp(ras-v) ` l(1)04-27 ras--v- Fs(1)10A+ Df(1)Sp(rb) - l(1)15-81 cho+ mei-9--peb- ( Cytology by Lefevre, who finds l(1)3Ad included. | Does not complement Df(1)sta = Df(1)1D3-E1;2A. / Spontaneous in a cross between wild-type males and mei-9 females. ` Covered by Dp(1;2)v+75d = Dp(1;2)9A2;10C2;40-41. - Complements Df(1)JC70 = Df(1)4C15-16;5A1-2. # Df(1)St472 cytology: Df(1)2B6-8;2B11-12. origin: X ray induced. discoverer: Pak. references: Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kramers, and Zhimulev, 1982, DIS 58: 184-90. genetics: Deficient for dor-fmf. # Df(1)sta: see Tp(1;3)sta # Df(1)su(f): Deficiency (1) suppressor of forked origin: X ray induced. deficiency cytology ref ( genetics | ____________________________________________________ Df(1)su(f)4B / 20A;20F 2, 4 wap--su(f)- bb+ Df(1)su(f)5A 20A;20F 1, 3 wap--su(f)- bb+ Df(1)su(f)724 20B;20F 1 stn--su(f)- Df(1)su(f)733 20D;20F 1 l(1)20Cb--su(f)- Df(1)su(f)754 20A;20F 1 eo--su(f)- Df(1)su(f)795 20A;20F 1 uncl--su(f)- Df(1)su(f)7009 20B;20F 1 stn--su(f)- Df(1)su(f)7085 19E;20F 1 unc--su(f)- Df(1)su(f)9122 19F;20F 1 fli-I--su(f)- ( 1 = Lifschytz and Yakobovitz, 1978, Mol. Gen. Genet. 161: 275-84; 2 = Schalet; 3 = Schalet and Lefevre, 1973, Chromosoma 44: 183-200; 4 = Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307. | Constitution with respect to bb not provided. / Induced in In(1)scS1Lsc8R In(1)dl-49 (Schalet). # Df(1)su(s): Deficiency (1) suppressor of sable deficiency genetics ______________________________ Df(1)su(s)2 l(1)1Bg--brc- Df(1)su(s)3 l(1)1Bg--brc- Df(1)su(s)4 l(1)1Bb--l(1)Ca- # Df(1)su(s)83 cytology: Df(1)1B10;1D6-E1 (Lefevre; Voelker). origin: / ray induced in y cho chromosome (Flemming). references: Voelker, Huang, Wisely, Sterling, Bainbridge, and Hiraizumi, 1989, Genetics 122: 625-42. genetics: Deficient for su(s). # Df(1)su(s)E2 references: Voelker. genetics: Deficient for l(1)1Bg - l(1)1Bk. # Df(1)svr: Deficiency (1) silver cytology: Df(1)1A1;1B9-10 (Lefevre). An apparently terminal deficiency. origin: Found among progeny of cold-treated female. discoverer: L. V. Morgan. references: 1940, DIS 13: 51. Sutton, 1943, Genetics 28: 213. Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53. White, 1980, Dev. Biol. 80: 332-34. Kramers, Schalet, Paradi, and Huiser-Hooteyling, 1983, Mutat. Res. 107: 187-201. genetics: Deficient for l(1)1Aa - vnd but not su(s) or sta. Embryonic lethal; abnormal development of nervous system and cell lethal (Ripoll and Garcia-Bellido). # Df(1)Sxl-bt: Deficiency (1) Sex-lethal cytology: Df(1)6E2;7A6. references: Nicklas and Cline, 1983, Genetics 103: 617-31. Cline, 1984, Genetics 107: 231-77. Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307. genetics: Deficient for l(1)6Eb - l(1)7Aa. # Df(1)Sxl-ra cytology: Df(1)6F5;7B1 (Lim); Df(1)7A1;7B3 (Wieschaus et al., 1984). origin: Revertant of dominant male lethality of SxlM#1. discoverer: Cline. references: Nicklas and Cline, 1983, Genetics 103: 617-31. Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307. genetics: Deficient for Sxl-l(1)7Ad. # Df(1)T origin: Induced by triethylenemelamine. references: Lim and Snyder, 1974, Genet. Res. 24: 1-10. deficiency cytology ____________________________ Df(1)T3 ( 1A1-2;1A7-8 Df(1)T4 1A1-2;1A5-6 Df(1)T9A 11D3-5;11D10-E1 Df(1)T9B 12A2-4;12A9-B1 Df(1)T19 1A1-2;1A8-B1 Df(1)T24 16A6-B1;16B2-4 Df(1)T30 3C6-7;3C8-9 Df(1)T34 2C2-4;2C10-D1 Df(1)T36 11A3-5;11A10-11 ( Deficient for l(1)1Ac - cin. # Df(1)T2-4A cytology: Df(1)19B3;19C4. origin: Tritiated deoxycytidine. discoverer: Kaplan. synonym: l(1)t2-4a. references: Schalet and Finnerty, 1968, DIS 43: 128-29. Schalet and Lefevre, 1976, The Genetics and Biology of Droso- phila (Ashburner and Novitski, eds.). Academic Press, Lon- don, New York, San Francisco, Vol. 1b, pp. 846-902. genetics: Deficient for sw-mel; lethal with sw and mutant with mel. # Df(1)T2-14A cytology: Df(1)19E5-6;19E7-8. origin: Induced by tritiated dioxycytidine. discoverer: Kaplan. synonym: l(1)t2-14a. references: Schalet and Finnerty, 1968, DIS 43: 128-29. Schalet and Lefevre, 1976, The Genetics and Biology of Droso- phila (Ashburner and Novitski, eds.). Academic Press, Lon- don, New York, San Francisco, Vol. 1b, pp. 846-902. genetics: Deficient for lf-vao. Viable with Df(1)16-3-35 (Schalet and Lefevre, 1976) in spite of the cytology listed for the deficiencies. # Df(1)T100 - Df(1)T138 origin: Induced by methyl methanesulfonate. references: Paradi, Vogel, and Szilagyi, 1983, Mutat. Res. 111: 145-59. genetics: Recessive lethal. deficiency cytology _________________________ Df(1)T100 19D-E;20A Df(1)T101 19F;20F Df(1)T103 19E;20F Df(1)T105 20A;20F Df(1)T106 19E-F;19F Df(1)T107 ( 19C;20A Df(1)T110 20B;20F Df(1)T113 19C;20A Df(1)T114 ( 19F;19F-20A Df(1)T122 19F;20A Df(1)T123 19F;20F Df(1)T124 ( 19D-E;20F Df(1)T136 ( 20B;20F Df(1)T137 ( 20A;20F Df(1)T138 ( 19E;20F ( Double mutant. #*Df(1)t282-1: Deficiency (1) tan cytology: Df(1)8C2-3;8C14-D1 (Sutton). Green and Green (1956, Z. Indukt. Abstamm. Vererbungsl. 87: 708-21) suggested that the deficiency probably extends farther to the right. origin: X ray induced. discoverer: Demerec, 34c. references: CP627. genetics: Deficiency for t, lz, and amx but not dd, dvr, flp, ny, or ras. # Df(1)TEM origin: Induced by triethylenemelamine. references: Lim and Snyder, 1974, Genet. Res. 24: 1-10. deficiency cytology ref ( genetics ______________________________________________________________ Df(1)TEM1 2E2-F1;3C1-2 1, 3, 5, 6 kz--w- Df(1)TEM6 2F5-3A1;3A3 3 gt--z- Df(1)TEM7 3A3;3B3 3,4 l(1)3Ac--l(1)3Bc- Df(1)TEM75 2F5-3A1;3C2-4 3 gt--w- Df(1)TEM202 | 3B2;3C3-5 3, 4 l(1)3Bb--w- Df(1)TEM304 2E2-F1;3A4-6 1, 3, 4 l(1)2Fd--l(1)3Ac- Df(1)TEM501 2E1;3C1-3 1, 2, 3 kz--w- ( 1 = Gvozdev, Gerasimova, Kovalev, and Ananiev, 1977, DIS 52: 67-68; 2 = Lim, 1979, Genetics 93: 681-701; 3 = Lim and Snyder, 1974, Genet. Res. 24: 1-10; 4 = Liu and Lim, 1975, Genetics 79: 601-11; 5 = Raymond, Laverty, and Sim- mons, 1986, DIS 63: 111-14; 6 = Simmons, Raymond, Culbert, and Laverty, 1984, Genetics 107: 49-63. | Deletion includes per (Bargiello, Jackson, and Young, 1984, Nature 312: 752-54; Bargiello and Young, 1984, Proc. Nat. Acad. Sci. USA 81: 2142-46). Molecular data show left breakpoint approximately 108 kb distal to wa copia inser- tion point (Pirrotta, Hadfield, and Pretorius, 1983, EMBO J. 2: 927-34; Reddy, Zehring, Wheeler, Pirrotta, Hadfield, Hall, and Rosbach, 1984, Cell 38: 701-10). # Df(1)v: Deficiency (1) vermilion origin: X ray induced. deficiency cytology ref ( genetics ____________________________________________________________________________ *Df(1)v63i 9D4-E1;10A11-10B1; see Dp(1;2)v+63i Df(1)v64f | 9E7-8;10A1-2 1, 2, 3, 4, 9 ras+ l(1)9Fa--l(1)10Aa- Df(1)v65b 9F13-10A1;11A7-8; see T(1;2)v65b Df(1)v73 / 10A2;10A5 6 sev--l(1)10Ac- *Df(1)v166 10A1-2;10A6-8 3 v--l(1)10Ac- Df(1)v-B151 9A1-4;10A1-2 8 v- Df(1)v-JA22 9F13;10A1 5 v- Df(1)v-L1 10A1;10A5; see T(1;3)vL1 Df(1)v-L2 9F13;10A1 3, 4, 9 l(1)9Fg--l(1)10Aa- Df(1)v-L3 9F10;10A7-8 3, 4, 9 fliG--l(1)10Ae- rtv+ Df(1)v-L4 9F5-6;10A1-2 3, 4, 9 ras+ sbr--l(1)10Aa- *Df(1)v-L5 9E8-10;10A1-2 3 ras+ v- *Df(1)v-L6 9E1-2;10A1-2 3 ras--v- Df(1)v-L7 9E1-2;10A1-2 3, 9 ras--l(1)10Aa- Df(1)v-L8 9D3-4;10A1-2; see T(1;2;3)vL8 *Df(1)v-L9 9D2;10A1-2 3 ras--v- *Df(1)v-L10 9D2;10A6-8 3 ras--v- Df(1)v-L11 9C4;10A1-2 3, 9 ras--l(1)10Aa- *Df(1)v-L12 9C1;10A2-6 3 ras--v- *Df(1)v-L13 9B13-14;10A1-2; see T(1;3)vL13 *Df(1)v-L14 9B10-11;10A2-6 3 ras--v- Df(1)v-L15 9B1-2;10A1-2 3, 7, 9 Hk--l(1)10Aa- *Df(1)v-L16 9F3-5;10A1-2 4 ras+ v- Df(1)v-M1 9D3;10A1-2 9, 10 ras--l(1)10Aa- Df(1)v-M5 9F13;10A1-2 9, 10 v--l(1)10Aa- Df(1)v-M6 9F11-12;10A1-2 9, 10 l(1)9Fg--l(1)10Aa- Df(1)v-M7 9D3;10A1-2 9, 10 ras--l(1)10Aa- Df(1)v-N48 see Tp(1;1)vN48 Df(1)v-P5 9D1-2;10A1-2 9, 10 ras--l(1)10Aa- Df(1)v-P22 ` 10A1;10A2 9, 10 v--l(1)10Aa- Df(1)v-VAM19 9E1;10A 5 v- ( 1 = Craymer and Roy, 1980, DIS 55: 200-04; 2 = Green; 3 = Lefevre, 1969, Genetics 63: 589-600; 4 = Lefevre, 1971, Genetics 67: 497-513; 5 = Perrimon, Engstrom, and Mahowald, 1989, Genetics 121: 333-52; 6 = Ripoll and Garcia-Bellido, 1979, Genetics 91: 443-53; 7 = Wieschaus, Nusslein-Volhard, and Jurgens, 1984, Wilhelm Roux's Arch. Dev. Biol. 193: 296-307; 8 = Zhimulev, Pokholkova, Bgatov, Umbetova, Solovjeva, Khudyakov, and Belyaeva, 1987, Biol. Zentrabl. 106: 699-720; 9 = Zhimulev, Belyaeva, Pokholkova, Kochneva, Fomina, Bgatov, Kudyakov, Patzevich, Semeshin, Baritcheva, Aizenzon, Kramers, and Eeken, 1982, DIS 58: 210-14; 10 = Zhimulev, Semeshin, and Belyaeva, 1981, Chromosoma 82: 9-23. | 10A1-2 breakpoint mapped to a restriction fragment at -2.7 to -1.3 kb (Hafen, Kasler, Edstrom, and Rubin, 1987, Science 236: 55-63); see molecular biology under sev for coordi- nates). / Lethal in germ-line clones (Garcia-Bellido and Robbins, 1983, Genetics 103: 235-47). ` / ray induced in T(1;Y)B149. # Df(1)V51: Deficiency (1) Valencia cytology: Df(1)19E1-2;19E3-4. origin: X ray induced. references: Valencia, 1970, DIS 45: 37-38. #*Df(1)vB: Deficiency (1) vermilion of Bridges origin: Spontaneous. discoverer: Bridges, 16e9. references: 1919, J. Gen. Physiol. 1: 645-56. genetics: Deficient for v. Genetic map shortened 1-3 units. # Df(1)VE624 cytology: Df(1)7E4;8B. discoverer: Lefevre. references: Perrimon, Engstrom, and Mahowald, 1989, Genetics 121: 333-52. # Df(1)VE696 cytology: Df(1)19F1;20F. discoverer: Lefevre. references: Perrimon, Engstrom, and Mahowald, 1989, Genetics 121: 333-52. # Df(1)vt: Deficiency (1) verticals cytology: Df(1)3C2-3;3C6-7 inferred from Young and Judd's fig- ure 1 (1978). references: Young and Judd, 1978, Genetics 88: 723-42. genetics: Deficient for rst-vt. # Df(1)wm4Lrst3R: see In(1)wm4Lrst3R # Df(1)wm4LwmJR: see In(1)wm4LwmJR # Df(1)wmaN: Deficiency (1) white-marbled Notch cytology: Df(1)3C2-3;3E2-3. origin: X ray induced. references: Lefevre and Moore, 1968, Genetics 58: 557-71. genetics: Deficient for rst, spl, dm, and N. Heterozygous females viable and fertile. Eyes "white-marbled" (like wsp). # Df(1)wmJLrst3R: see In(1)wmJLrst3R # Df(1)w26d: Deficiency (1) white cytology: Deletion of 3C2-6 + interband 3C6-7; 3C1 "fused" to 3C7, forming a thick band. origin: Df(1)w67k30 + Df(1)fa-swb recombinant. references: Keppy and Welshons, 1977, Genetics 85: 497-506. 1980, Chromosoma 76: 191-200. genetics: Deficient for w, rst, and vt. faswb phenotype absent although faswb can be recovered as a recombinant product from Df(1)w26D. # Df(1)w55j cytology: 3C2;3C2. origin: Unequal recombination in wa/wa4 female. references: Green, 1959, Heredity 13: 303-15. 1963, Z. Indukt. Abstamm. Vererbungsl. 94: 200-14. Goldberg, Paro, and Gehring, EMBO J. 1: 93-98. genetics: Homozygous viable. Deficient for wsp and we sites. molecular biology: Copia insertion near breakpoint. # Df(1)W61 cytology: Df(1)10B8;10E1-2. genetics: Deficient for RpII215. # Df(1)w62g26: see Tp(1;2)w+62g # Df(1)w63b: see Df(1)N63b # Df(1)w64b: see T(1;2)w+64b # Df(1)w64c cytology: Df(1)2D6-E1;3C2-3. origin: X ray induced. discoverer: Lefevre, 64c18. references: Stewart and Merriam, 1974, Genetics 76: 301-09. Craymer and Roy, 1980, DIS 55: 200-04. genetics: Deficient for pn, gt, and w. # Df(1)w64d: see In(1)w-64d # Df(1)w67 origin: Derived from mutable w8, except for X-ray-induced Df(1)w67k30. male deficiency cytology syn. ref ( genetics viab.? ___________________________________________________________________ Df(1)w67c2 | 3C1-2;3C2-3 w-1 1,2,6 w- rst+ vt+ + Df(1)w67c3 3C1-2;3C3-4 w-4 5, 6 w- rst+ vt+ + / Df(1)w67c9 3C1-2;3C2-3 w-2 6 w- rst+ vt+ + Df(1)w67c11 3C1-2;3C5-6 wrv-4 6, 8 w- rst- vt+ + / Df(1)w67c14 3C1-2;3C5 wr-2 6 w- rst_ vt+ + / Df(1)w67c23 3C1-2;3C5 wv-1 6 w- rst+ vt- + / Df(1)w67c23.1 3C1-2;3C5 wrv-1 6 w- rst_ vt_ + / Df(1)w67c23.2 3C1-2;3C6-7 wrv-5 6 w- rst- vt- - Df(1)w67d4 3C1-2;3C6-7 wrv-6 6 w- rst- vt- - Df(1)w67d7 3C1-2;3C3-4 w-3 6 w- rst+ vt+ + / Df(1)w67d17 3C1-2;3C5 wr-3 6 w- rst_ vt+ + / Df(1)w67d22 3C1-2;3C5-6 wrv-2 6 w- rst- vt- + / Df(1)w67d24 3C1-2;3C5-6 wrv-3 6, 8 w- rst- vt- + / Df(1)w67d38 3C1-2;3C5 wr-1 6 w- rst_ vt+ + / Df(1)w67e8 ` 3C1-2;3C6-7 wrv-7 3,6,8 w- rst- vt- - Df(1)w67k30 `- 3C1-2;3C6-7 wrv-X 4,6,7 w- rst- vt- - ( 1 = Goldberg, Paro, and Gehring, 1982, EMBO J. 1: 93; 2 = Green, 1969, Genetics 61: 429-41; 3 = Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82; 4 = Lefevre, 1970, DIS 45: 32; 5 = Lefevre and Green, 1971, DIS 46: 141; 6 = Lefevre and Green, 1972, Chromosoma 36: 391- 412; 7 = Ripoll and Garcia-Bellido, 1978, Genetics 91: 443-53; 8 = Welshons and Welshons, 1985, Genetics 110: 465-77. | Molecular biology: 3C2-3 (right or proximal) breakpoint between 2.4 and 3.5 kb to the right of the wa copia inser- tion point (Pirrotta and Brockl, 1984, EMBO J. 3: 563-68; Pirrotta, Hadfield, and Pretorius, 1983, EMBO J. 2: 927- 34). / Slow to emerge. ` Cell viable. - Covered by Dp(1;3)wvco. Suppresses faswb. Deletes 5' half of the transcription unit immediately upstream of N (Kidd, Kelley, and Young, 1986, Mol. Cell Biol. 6: 3094-3108). # In(1)w-68b15 - In(1)w-71a27.1 origin: X ray induced in In(1)z+64b9=In(1)3C1-2;12B8-9. references: Sorsa, Green, and Beerman, 1973, Nature (London), New Biol. 245: 34-37. inversion cytology new order genetics _______________________________________________________________________ In(1)w-68b15 3Cl;11F3;12B8 1A - 3C1|11F3 - 12B8| male viable; 11F2 - 3C1|12B9 - 20 zv w- In(1)w-70L26.3 4C;12A + 1A - 3B|12B|4C - 12A| male lethal; Df(1)3B;3C1 + 4C - 3C2|12B9 - 20 crm+ w- g+ Df(1)12A;12B8-9 In(1)w-70L26.8 3Cl;12B1;12B8 1A - 3C1|12B1 - 12B8| male viable; (reinversion) 12A10 - 3C2|12B9 - 20 zv w- In(1)w-71a9.3 1D1;3C1 1A - 1C5|3C1 - 1D1| male viable; 12B8 - 3C2|12B9 - 20 zv w- In(1)w-71a27.1 3Cl;11A1;12B8 1A - 3C1|11A1 -12B8| male viable 10F11 - 3C2|12B9 - 20 zv w- # Df(1)w78 cytology: Df(1)3C1-2;3C2-3; inferred from genetic data. origin: Spontaneous in Dp(1;1)wawsp, z male; simultaneous with recovery of transposon w+II(78h24). references: Rasmuson and Montell, 1980, DIS 55: 127. Rasmuson, Montell, Rasmuson, Svahlin, and Westerberg, 1980, Mol. Gen. Genet. 177: 567-70. genetics: Deficient for w but not for rst or vt. # Df(1)w79 cytology: Df(1)3C2-8;3C6-7 superimposed on In(1)3C1-2;3C7-8. origin: Spontaneous derivative of In(1)N66h26. new order: 1A - 3C1|3C7|3C8 - 20. 3C2-6 missing. references: Welshons and Keppy, 1981, Mol. Gen. Genet. 181: 319-24. genetics: Deficient for w, rst, vt, and N. # Df(1)w80k1 cytology: Df(1)3C2;3C2. origin: Spontaneous (presumably induced by recombination between FB elements). references: Collins and Rubin, 1984, Nature 308: 323-27. genetics: Mutant for w. Male viable and fertile. molecular biology: Sequences within wc insertion partially deleted and sequences in left copy of the wi duplication absent. # Df(1)w86.8 references: Kaufman, Tasaka, and Suzuki, 1973, Genetics 75: 299-321. genetics: Dominant suppressor of z and za. Deficient for w. # Df(1)W172 cytology: Df(1)10A1-2;11A1-2. genetics: Deficient for RpII215. # Df(1)w258 origin: X ray induced. discoverer: Demerec. deficiency cytology ref ( genetics ________________________________________________________________ Df(1)w258-3 3B2-3;3C1-2 br+ w- fa+ Df(1)w258-11 3A2-3;3C3-5 1, 2, 4 kz+ z--w- rst+; embryonic lethal *Df(1)w258-14 3A3-4;3C2-3 4, 5 kz+ w- rst+ Df(1)w258-42 3A4-6;3C5-6 1, 2 kz+ l(1)3Ad--rst-; embryonic lethal Df(1)w258-45 | 3B2-3;3C2-3 1, 2, 3 kz+ l(1)3Bc--w- rst+; embryonic lethal Df(1)w258-48 3A9-B1;3C2-3 5 kz+ w- rst+ ( 1 = Judd, Shen, and Kaufman, 1972, Genetics 71: 139-56; 2 = Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82; 3 = Lefevre, 1968, DIS 43: 141, 165; 4 = Slizynska, 1938, Genetics 23: 291-99; 5 = Wright, 1970, Adv. Genet. 15: 261-395. | Proximal member of double deficiency Df(1)64j4 Df(1)w258-45 (Kaufman et al., 1975). Germ-line clones lethal (Garcia- Bellido and Robbins, 1983, Genetics 103: 235-47). Defi- ciency extends from 85-90 kb to the left to approximately 65 kb to the right of the wa copia insertion point (Pirrotta, Hadfield, and Pretorius, 1983, EMBO J. 2: 927-34; Reddy, Zehring, Wheeler, Pirrotta, Hadfield, Hall, and Rosbach, 1984, Cell 38: 701-10). # Df(1)w-c: Deficiency (1) white-crimson cytology: Df(1)3C2;3C2. origin: Spontaneous (presumably induced by recombination between FB elements). references: Collins and Rubin, 1984, Nature 308: 323-27. genetics: Mutant for w. Male viable and fertile. molecular biology: Sequences adjacent to and extending to the left of the wc insertion are deleted, while sequences to the right are conserved. Restriction maps of the following six deletions have been made: Df(1)w-c80j2, Df(1)w-c81b1, Df(1)w-c81b4, Df(1)w-c81b8, Df(1)w-c82a2, and Df(1)w-c82d1. # Df(1)w-DZL origin: In wDZL/wDZL females. Presumed to be a rearrangement generated by wDZL. deficiency cytology ref ( genetics __________________________________________________________ Df(1)w-DZL-1 3A2-4;3C1-2 1 l(1)3Bf--w- Df(1)w-DZL-2 | / 3C1-2;3D2-3 1, 2, 3, 4 wDZL- -N- Df(1)w-DZL-3 3B4-5;3C1-2 1 l(1)3Bf--w- Df(1)w-DZL-14 | ` 3C1-2;3C7-9 1, 2, 3 wDZL- -N- ( 1 = Bingham, 1980, Cold Spring Harbor Symp. Quant. Biol. 45(2): 519-25; 2 = Bingham, Levis, and Rubin, 1981, Cell 25: 693-704; 3 = Zachar and Bingham, 1982, Cell 30: 529- 41; 4 = Bingham and Zachar, Cell 40: 819-25. | Df(1)w-DZL-2 begins at or very near the right-hand FB seg- ment of the wDZL transposon, removing sequences at or near the transposon insertion and extending to the right (away from w) for several hundred kilobases, leaving the w locus, the unique sequence, and the left-hand FB segment of the wDZL transposon (Bingham and Zachar, 1985, Cell 40: 819- 25). The left breakpoint of Df(1)w-DZL-14 lies between coordinates +8.0 and +10.6, with 0 the site of the copia insertion in wa (Levis, Bingham, and Rubin, 1982, Proc. Nat. Acad. Sci. USA 79: 564-68). / Associated with wDZL; removes sequence at/or near the wDZL TE insertion and extending proximally (Bingham and Zachar, 1982). ` Associated with w+; lacks most of wDZL TE (Zachar and Bing- ham, 1982). # Df(1)w-ec: see Tp(1;2)w-ec # Df(1)w-m49a: see Tp(1;3)wm49a #*Df(1)w-m53a: see Tp(1;2)wm53a # Df(1)w-N14a: Deficiency (1) white to Notch cytology: Df(1)2C8-9;3E3-4. origin: X ray induced. discoverer: Lefevre. genetics: Deficient for usp-slc. # Df(1)w-N71a cytology: Df(1)3A4-6;3C10-11. origin: Spontaneous in crossover experiment involving Df(1)N- 54l9/w females. discoverer: Lefevre. references: Judd, Shen, and Kaufman, 1972, Genetics 71: 139- 56. Craymer and Roy, 1980, DIS 55: 200-04. genetics: Deficient for l(1)3Ad. # Df(1)w-NFM20 cytology: Df(1)3C1-2;3C7-D1 (Bingham). references: McGinnis, Farrell, and Beckendorf, 1980, Proc. Nat. Acad. Sci. USA 77: 7367-71. genetics: Deficient for w, N, and Sgs-4. molecular biology: Lacks w and Sgs-4 sequences. # Df(1)w-r: Deficiency (1) white-recombinant origin: Regular product of unequal exchange between 3C1-2 (or 3) of a wa, wa2, or wrdp chromosome and the 3A or 3C-D region of a specific homologue. deficiency cytology ref ( genetics _______________________________________________________________________ Df(1)w-rG 3A3-4;3C1-2 1 z+ w- (or w) rst+ Df(1)w-rJ1 | 3A1-2;3C2-3 2, 3, 4, 5 gt+ tko--w- (or w) rst+; embryonic lethal and lethal in germ-line clones / Df(1)w-rJ2 3A8-9;3C2-3 2, 3, 4, 5 l(1)3Ag+ l(1)3Ah--w- (or w) rst+; embryonic lethal Df(1)w-rJ3 ` 3C1-2;3C12-D1 2, 3 w- (or w) -dm- (or dm) ( 1 = Green, 1959, Genetics 44: 1243-56; 2 = Judd, 1961, Genetics 46: 1687-97; 3 = Judd, 1964, DIS 39: 59-60; 4 = Judd, Shen, and Kaufman, 1972, Genetics 71: 139-56; 5 = Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82. | Survives as w female when heterozygous with Df(1)wm4L rst3R; such females display reduced crossing over and increased nondisjunction for all pairs of homologues. Deletes per locus (Bargiello and Young, 1984, Proc. Nat. Acad. Sci. USA 81: 2142-46). Molecular biology: 3A3-4 (left or distal) breakpoint local- ized to an approximately 4-kb restriction fragment 2-6 kb to the left of the origin of a 160-kb walk in the vicinity of z (Gunaratne, Mansukhani, Lipari, Liou, Martindale, and Gold- berg, 1986, Proc. Nat. Acad. Sci. USA 83: 701-05). / According to Garcia-Bellido and Robbins, 1983, Genetics 103: 235-47. ` Survives as w female when heterozygous with Df(1)w258-45, Df(1)w-rJ1, or Df(1)w-rJ2. # Df(1)w-vco: see Tp(1;3)wvco # Df(1)w-Vogt cytology: Df(1)3A9-B1;3C3-4. references: Wright, 1970, Adv. Genet. 15: 261-395. genetics: Deficient for w. Lethal phase in embryo. # Df(1)w-zh: see Tp(1;3)wzh # Df(1)wl-2 cytology: Df(1)19E6;20F. origin: X ray induced. references: Lifschytz and Falk, 1969, Mutat. Res. 8: 147-55. genetics: Deficient for lf-bb. # Df(1)wrv: see Df(1)w67 # Df(1)wy2: Deficiency (1) wavy cytology: Df(1)11A6-12;11F2-4. origin: X ray induced. discoverer: Goralski. genetics: Deficient for M(1)11F and wy. # Df(1)wy26 cytology: Df(1)11B17-C1;11E9-10. origin: X ray induced. discoverer: Goralski. genetics: Deficient for wy. # Df(1)X1 cytology: Df(1)20D-E;20F. origin: X ray induced. references: Lifschytz and Falk, 1969, Mutat. Res. 8: 147-55. Schalet and Lefevre, 1973, Chromosoma 44: 183-200. Rahman and Lindsley, 1981, Genetics 99: 49-64. genetics: Deficient for sph-bb. Male viable and fertile with BSYy+, viable and sterile with y+Ymal+. # Df(1)X10 cytology: Df(1)2F5-3A1;3C3; status of 2F6 in doubt. origin: X ray induced. discoverer: R. Falk. references: Lifschytz, 1967, DIS 42: 89. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82. Lifschytz and Green, 1984, EMBO J. 3: 999-1002. genetics: Deficient for gt-w; covered by w+Y (Lifschytz, 1967). Lethal in embryonic period. Used as marker for z- w- (Lifs- chytz and Green, 1984). # Df(1)X12 cytology: Df(1)2F6-3A1;3B5-3C1; status of 2F6 in doubt. origin: X ray induced. discoverer: R. Falk. references: Lifschytz, 1967, DIS 42: 89. Kaufman, Shannon, Shen, and Judd, 1975, Genetics 79: 265-82. Lifschytz and Green, 1984, EMBO J. 3: 999-1002. Perrimon, Engstrom, and Mahowald, 1984, Genetics 108: 559-72. genetics: Deficient for phl-l(1)3Bf. Lethal in embryonic period. Used as marker for z- w- (Lifschytz and Green, 1984). # Df(1)X15: see Df(1)y-X15 # Dp(1;Y)y2: Duplication (1;Y) yellow origin: / ray induced in attached -XY, y2 su(wa) wa males. discoverer: Gorelova. synonym: y2Y. duplication cytology ref ( genetics ________________________________________________ Dp(1;Y)y221T 1A;2B6(2B7-8?) 1,2 y+-hfw+ Dp(1;Y)y222T 1A;2B9-10 1 y+-fmf+ Dp(1;Y)y240T 1A;2B9-11 1,2 y+-fmf+ Dp(1;Y)y243T 1A;2E1-2 1 Dp(1;Y)y253T 1A;2B6(2B7-8?) 1,2 y+-hfw+ ( 1 = Belyaeva, Aizenzon, Kiss, Gorelova, Pak, Umbetova, Kra- mers, and Zhimulev, 1982, DIS 58: 184-90; 2 = Belyaeva, Aizenzon, Semeshin, Kiss, Koczka, Baritcheva, Gorelova, and Zhimulev, 1980, Chromosoma 81: 281-306. # Df(1)y3PLsc8R: see In(1)y3PLsc8R # Df(1)y4Lsc4R: see In(1)y4Lsc4R # Df(1)y4Lsc8R: see In(1)y4Lsc8R # Df(1)y4Lsc9R: see In(1)y4Lsc9R # Df(1)y74 - Df(1)y75 deficiency cytology origin ( ref | genetics ______________________________________________________________________________ Df(1)y74i4.2 / 1A1;1B4 1 2, 3 l(1)1Aa--sc- Df(1)y74k10.1 1A1;1B5-6 1 2, 3, 5 l(1)1Aa--l(1)Bh- l(1)Bi+ Df(1)y74k10.3 1A1;1B5-6 1 2, 3 l(1)1Aa--sc- Df(1)y74k24.1 1A1;1B9-10 1 1, 2, 3, 5 l(1)1Aa--l(1)1Bi- su(s)+ Df(1)y74k24.2 1A1;1B5-6 1 2, 3 l(1)1Aa--sc- Df(1)y75a22.1 1A1;1B5-6 1 3 l(1)1Aa--sc- Df(1)y75e 1A1;1B6-9 2 4 l(1)1Aa--sc- ( 1 = y2 mutator stock of M.M. Green; 2 = TEM. | 1 = Craymer and Roy, 1980, DIS 55: 200-04; 2 = Garcia- Bellido, 1979, Genetics 91: 491-520; 3 = Lefevre; 4 = Lim, 1979, Genetics 93: 681-701; 5 = Voelker. / Viable and strong sc over Dp(1;4)sc-H (Garcia-Bellido, 1979). # Df(1)y-A: Deficiency (1) yellow of Alexandrov references: Alexandrov, Ankina, and Alexandrova, 1985, DIS 61: 212-13. deficiency cytology origin ( genetics _________________________________________________ Df(1)y-A71k2 1B1;1B2 3 y34C- Df(1)y-A71l1 1B1;1B2 3 y- Df(1)y-A72d2 1B1;1B2 3 y- Df(1)y-A74b151 1B1;1B2 2 y- Df(1)y-A74d2 1B1;1B2 3 y- Df(1)y-A74d30 1B1;1B2 2 y- Df(1)y-A74d40 1B1;1B2 2 y- Df(1)y-A74e2 1B1;1B2 2 y- Df(1)y-A74k 1B1;1B2 3 yc4- Df(1)y-A75l1 1B1;1B2 3 y- Df(1)y-A75l3 1B1;1B2 3 y- Df(1)y-A76i 1B1;1B2 1 y- Df(1)y-A76j 1B1;1B2 1 yc4- Df(1)y-A76k 1B1;1B2 1 yc4- Df(1)y-A77a 1B1;1B2 1 y- Df(1)y-A78a 1B1;1B2 1 y- Df(1)y-A78d | 1A3;1B1-2 3 lethal Df(1)y-A79b / 1A5-6;1B6 4 lethal Df(1)y-A79d1 | 1A3;1B1-2 3 lethal Df(1)y-A79h2 | 1A3;1B1-2 3 lethal Df(1)y-A82c38 / 1A6;1B4 4 lethal ( 1 = actinomycin-D and / rays; 2 = caffeine and / rays; 3 = ( rays; 4 = neutrons. | Df(1)y/y+Y males not viable. / Df(1)y/y+Y males viable. # Df(1)y-ac: Deficiency (1) yellow-achaete references: Biessmann and Mason, 1988, EMBO J. 7: 1081-86. Walter, Black, Afshar, Kermabon, Wright, and Biessmann, 1990. phenotype: Homozygous viable y-ac deficiency. molecular biology: Removes entire y gene coding region (Biessmann and Mason, 1988). # Df(1)y-X: Deficiency (1) yellow-X ray origin: All deficiencies X ray induced in In(1)sc8 with the exception of Df(1)y-X2rl. deficiency cytology ref ( genetics ________________________________________________________________________ Df(1)y-X2 deletion of X tip 3, 4 l(1)1Ac--ac-, bb-; + part of 20F (170 rRNA sequences); covered by y+Y; Df/bb females bb Df(1)y-X2rl | deletion of X tip 1, 4 l(1)1Ac--ac- bbl + more of 20F Df(1)y-X5 deletion of X tip 5, 6 l(1)1Ac--ac-, + 20A4-5 fog--bb- through 20F; capped by 2L(?) Df(1)y-X7 deletion of X tip 3 l(1)1Ac--ac-, + 20C-D l(1)20Cb--bb-; through 20F males viable with BSYy+ and y+Ymal+ Df(1)y-X9 deletion of X tip 3 l(1)1Ac--ac-, + 20B-C fog--bb-; through 20F males lethal with BSYy+, viable with y+Ymal+ Df(1)y-X15 deletion of X tip 2, 3, 5 l(1)1Ac--ac-, + 20D-E sph--bb-; through 20F + males with y+Y inversion with lethal, with 8C break capped by 4 / BSYy+ viable and fertile, with y+Ymal+ viable and sterile. Df(1)y-X16 deletion of X tip 3 l(1)1Ac--ac-, + 20B-C fog--bb-; through 20F males with BSYy+ lethal, with y+Ymal+ viable ( 1 = Procunier and Tartof, 1978, Genetics 88: 67-79; 2 = Rahman and Lindsley, 1981, Genetics 99: 49-64; 3 = Schalet, 1968, DIS 43: 64; 4 = Schalet, 1969, Genetics 63: 133-53; 5 = Schalet and Lefevre, 1973, Chromosoma 44: 184-200; 6 = Zusman and Wieschaus, 1987, Genetics 115: 725-36. | Derived from Df(1)y-X2 by reduction in number of rDNA genes under the influence of Ybb-. / new order: 102-101|8C - 20D|8C - 1B|20F. # Df(1)yl-1 cytology: Df(1)19E6;20A1-2. origin: X ray induced. references: Lifschytz and Falk, 1969, Mutat. Res. 8: 147-55. genetics: Deficient for lf-eo. # Df(1)yT: Deficiency (1) yellow Terminal cytology: Putative terminal deficiencies with breaks between 1B1 and 1F. origin: Irradiation of mu-2 females (Mason, Strobel, and Green, 1984, Proc. Nat. Acad. Sci. USA 81: 6090-94; Biessman and Mason, 1988, EMBO J. 7: 1081-86). synonym: Df(1)yRT (Sherald and Voelker, 1985, DIS 61: 155). deficiency ( ref | genetics mol biol / ______________________________________________________ Df(1)yT1a-276 2, 3 y2- y1+ 71.5-69.5 Df(1)yT1a-394 2, 3 y2- y1+ 72.3-71.6 Df(1)yT1a-473 2, 3 y2- y1+ 72.3-71.6 Df(1)yT1a-653 2, 3 y2- y1+ 72.3-71.6 Df(1)yT1a-741 2, 3 y2- y1+ 71.5-69.5 Df(1)yT1b-81 2, 3 y1- ac+ 67.8-67.7 Df(1)yT1b-94 2, 3 y1- ac+ 67.7-67.2 Df(1)yT1b-96 2 y1- ac+ Df(1)yT1b-303 2, 3 y1- ac+ 67.2-66.3 Df(1)yT1b-488 2, 3 y1- ac+ 64.2-63.2 Df(1)yT1b-497 2, 3 y1- ac+ 65.6-65.3 Df(1)yT1b-625 2, 3 y1- ac+ 65.3-64.8 Df(1)yT1b-627 2 y1- ac+ Df(1)yT1b-628 2, 3 y1- ac+ 67.2-66.3 Df(1)yT1b-685 2, 3 y1- ac+ 45.4-43.9 Df(1)yT1b-688 2 y1- ac+ Df(1)yT1b-689 2, 3 y1- ac+ 67.2-66.3 Df(1)yT1b-733 2 y1- ac+ Df(1)yT2-26 2 ac- sc+ Df(1)yT2-29 2, 3 ac- sc+ 42.3-39.5 Df(1)yT2-83 2, 3 ac- sc+ 50.2-49.4 Df(1)yT2-84 2, 3 ac- sc+ 53.2-52.4 Df(1)yT2-85 2, 3 ac- sc+ 46.0-45.4 Df(1)yT2-86 2, 3 ac- sc+ 53.2-52.4 Df(1)yT2-89 2, 3 ac- sc+ 46.0-45.4 Df(1)yT2-90 2, 3 ac- sc+ 52.4-50.2 Df(1)yT2-92 2, 3 ac- sc+ 50.6-49.4 Df(1)yT2-93 2, 3 ac- sc+ 49.4-47.9 Df(1)yT2-95 2, 3 ac- sc+ 54.3-53.2 Df(1)yT2-97 2, 3 ac- sc+ 55.8-54.3 Df(1)yT2-99 2, 3 ac- sc+ Df(1)yT2-103 2, 3 ac- sc+ 42.1-41.5 Df(1)yT2-150 2, 3 ac- sc+ 33.8-33.4 Df(1)yT2-165 2, 3 ac- sc+ 45.4-43.9 Df(1)yT2-195 2, 3 ac- sc+ 62.4-61.8 Df(1)yT2-212 2, 3 ac- sc+ 56.8-56.3 Df(1)yT2-214 2, 3 ac- sc+ 33.4-32.7 Df(1)yT2-216 2, 3 ac- sc+ 52.4-50.6 Df(1)yT2-233 2, 3 ac- sc+ 38.4-36.3 Df(1)yT2-242 2, 3 ac- sc+ 61.2-60.3 Df(1)yT2-252 2, 3 ac- sc+ 42.1-41.5 Df(1)yT2-288 2, 3 ac- sc+ 46.0-45.4 Df(1)yT2-293 2, 3 ac- sc+ 57.6-56.6 Df(1)yT2-304 2, 3 ac- sc+ 44.4-43.9 Df(1)yT2-331 2, 3 ac- sc+ 61.2-60.3 Df(1)yT2-336 2, 3 ac- sc+ 47.9-46.8 Df(1)yT2-343 2, 3 ac- sc+ 36.6-33.8 Df(1)yT2-351 2, 3 ac- sc+ 47.9-46.8 Df(1)yT2-356 2, 3 ac- sc+ 52.4-50.6 Df(1)yT2-398 2, 3 ac- sc+ 58.9-58.2 Df(1)yT2-438 2, 3 ac- sc+ 50.6-49.4 Df(1)yT2-503 2, 3 ac- sc+ 54.3-53.2 Df(1)yT2-520 2, 3 ac- sc+ 52.4-50.6 Df(1)yT2-524 2, 3 ac- sc+ 42.3-42.1 Df(1)yT2-551 2, 3 ac- sc+ 42.3-39.5 Df(1)yT2-558 2, 3 ac- sc+ 58.9-58.2 Df(1)yT2-589 2, 3 ac- sc+ 62.9-62.4 Df(1)yT2-590 2, 3 ac- sc+ 52.4-50.6 Df(1)yT2-618 2, 3 ac- sc+ 39.5-37.1 Df(1)yT2-623 2, 3 ac- sc+ 45.4-44.4; 36.7-34.4 Df(1)yT2-624 2, 3 ac- sc+ 54.3-53.2 Df(1)yT2-626 2, 3 ac- sc+ 59.7-58.9 Df(1)yT2-629 2, 3 ac- sc+ 42.3-39.5 Df(1)yT2-630 2, 3 ac- sc+ 45.4-43.9 Df(1)yT2-631 2, 3 ac- sc+ 37.1-35.5 Df(1)yT2-633 2, 3 ac- sc+ 62.4-61.8 Df(1)yT2-634 2 ac- sc+ Df(1)yT2-637 2, 3 ac- sc+ 49.4-47.9 Df(1)yT2-643 2, 3 ac- sc+ 46.0-45.4 Df(1)yT2-650 2, 3 ac- sc+ 37.1-35.5 Df(1)yT2-655 2, 3 ac- sc+ 55.8-54.3 Df(1)yT2-659 2, 3 ac- sc+ 62.4-61.8 Df(1)yT2-691 2, 3 ac- sc+ 59.9-59.7 Df(1)yT2-695 2 ac- sc+ Df(1)yT2-696 2, 3 ac- sc+ 60.2-59.9; 53.2-52.4; 47.9-45.8 Df(1)yT2-701 2, 3 ac- sc+ 53.2-52.4 Df(1)yT2-730 2, 3 ac- sc+ 49.4-47.9 Df(1)yT2-734 2 ac- sc+ Df(1)yT2-735 2 ac- sc+ Df(1)yT2-738 2 ac- sc+ Df(1)yT2-739 2, 3 ac- sc+ 60.3-59.9 Df(1)yT2-742 2, 3 ac- sc+ 47.9-46.8 Df(1)yT2-744 2 ac- sc+ Df(1)yT2-748 2, 3 ac- sc+ 38.4-36.3 Df(1)yT2-749 2 ac- sc+ Df(1)yT3-15 2 sc- l(1)1Bb+ Df(1)yT3-22 2 sc- l(1)1Bb+ Df(1)yT3-24 2 sc- l(1)1Bb+ Df(1)yT3-55 2 sc- l(1)1Bb+ Df(1)yT4-8 2 l(1)1Bb- l(1)1Bc+ Df(1)yT4-19 2 l(1)1Bb- l(1)1Bc+ Df(1)yT4-20 2 l(1)1Bb- l(1)1Bc+ Df(1)yT4-25 2 l(1)1Bb- l(1)1Bc+ Df(1)yT6-151 2 svr- elav+ Df(1)yT6-188 2 svr- elav+ Df(1)yT6-244 2 svr- elav+ Df(1)yT6-291 2 svr- elav+ Df(1)yT6-437 2 svr- elav+ Df(1)yT6-450 2 svr- elav+ Df(1)yT6-506 2 svr- elav+ Df(1)yT6-522 2 svr- elav+ Df(1)yT6-544 2 svr- elav+ Df(1)yT7-104 2 elav- vnd+ Df(1)yT7-107 2 elav- vnd+ Df(1)yT7-108 2 elav- vnd+ Df(1)yT7-109 2 elav- vnd+ Df(1)yT7-114 2 elav- vnd+ Df(1)yT7-115 2 elav- vnd+ Df(1)yT7-129 2 elav- vnd+ Df(1)yT7-130 2 elav- vnd+ Df(1)yT7-155 2 elav- vnd+ Df(1)yT7-157 2 elav- vnd+ Df(1)yT7-178 2 elav- vnd+ Df(1)yT7-191 2 elav- vnd+ Df(1)yT7-194 2 elav- vnd+ Df(1)yT7-208 2 elav- vnd+ Df(1)yT7-218 2 elav- vnd+ Df(1)yT7-229 2 elav- vnd+ Df(1)yT7-234 2 elav- vnd+ Df(1)yT7-250 2 elav- vnd+ Df(1)yT7-263 2 elav- vnd+ Df(1)yT7-284 2 elav- vnd+ Df(1)yT7-292 2 elav- vnd+ Df(1)yT7-296 2 elav- vnd+ Df(1)yT7-301 2 elav- vnd+ Df(1)yT7-311 2 elav- vnd+ Df(1)yT7-329 2 elav- vnd+ Df(1)yT7-341 2 elav- vnd+ Df(1)yT7-348 2 elav- vnd+ Df(1)yT7-358 2 elav- vnd+ Df(1)yT7-366 2 elav- vnd+ Df(1)yT7-371 2 elav- vnd+ Df(1)yT7-376 2 elav- vnd+ Df(1)yT7-377 2 elav- vnd+ Df(1)yT7-400 2 elav- vnd+ Df(1)yT7-401 2 elav- vnd+ Df(1)yT7-404 2 elav- vnd+ Df(1)yT7-406 2 elav- vnd+ Df(1)yT7-435 2 elav- vnd+ Df(1)yT7-446 2 elav- vnd+ Df(1)yT7-448 2 elav- vnd+ Df(1)yT7-458 2 elav- vnd+ Df(1)yT7-518 2 elav- vnd+ Df(1)yT7-525 2 elav- vnd+ Df(1)yT7-532 2 elav- vnd+ Df(1)yT7-547 2 elav- vnd+ Df(1)yT8-9 2 vnd- l(1)Bg+ Df(1)yT8-12 2 vnd- l(1)Bg+ Df(1)yT8-18 2 vnd- l(1)Bg+ Df(1)yT8-101 2 vnd- l(1)Bg+ Df(1)yT8-124 2 vnd- l(1)Bg+ Df(1)yT8-128 2 vnd- l(1)Bg+ Df(1)yT8-143 2 vnd- l(1)Bg+ Df(1)yT8-148 2 vnd- l(1)Bg+ Df(1)yT8-158 2 vnd- l(1)Bg+ Df(1)yT8-184 2 vnd- l(1)Bg+ Df(1)yT8-185 2 vnd- l(1)Bg+ Df(1)yT8-197 2 vnd- l(1)Bg+ Df(1)yT8-206 2 vnd- l(1)Bg+ Df(1)yT8-241 2 vnd- l(1)Bg+ Df(1)yT8-271 2 vnd- l(1)Bg+ Df(1)yT8-361 2 vnd- l(1)Bg+ Df(1)yT8-362 2 vnd- l(1)Bg+ Df(1)yT8-368 2 vnd- l(1)Bg+ Df(1)yT8-369 2 vnd- l(1)Bg+ Df(1)yT8-385 2 vnd- l(1)Bg+ Df(1)yT8-409 2 vnd- l(1)Bg+ Df(1)yT8-420 2 vnd- l(1)Bg+ Df(1)yT8-500 2 vnd- l(1)Bg+ Df(1)yT8-530 2 vnd- l(1)Bg+ Df(1)yT9-7 2, 4 l(1)1Bg- l(1)Bh+ Df(1)yT9-21 2, 4 l(1)1Bg- l(1)Bh+ Df(1)yT9-220 2, 4 l(1)1Bg- l(1)Bh+ Df(1)yT9-275 2, 4 l(1)1Bg- l(1)Bh+ Df(1)yT10-102 2, 4 l(1)1Bh- l(1)Bi+ Df(1)yT10-106 2, 4 l(1)1Bh- l(1)Bi+ Df(1)yT10-581 2, 4 l(1)1Bh- l(1)Bi+ Df(1)yT10-665 2, 4 l(1)1Bh- l(1)Bi+ Df(1)yT10-673 2, 4 l(1)1Bh- l(1)Bi+ Df(1)yT10-677 2, 4 l(1)1Bh- l(1)Bi+ Df(1)yT12-173 2, 4 M(1)Bld- su(s)+ Df(1)yT12-187 2, 4 M(1)Bld- su(s)+ Df(1)yT12-200 2, 4 M(1)Bld- su(s)+ Df(1)yT12-206 2, 4 M(1)Bld- su(s)+ Df(1)yT12-246 2, 4 M(1)Bld- su(s)+ Df(1)yT12-667 2, 4 M(1)Bld- su(s)+ Df(1)yT13-423 ` 2, 4 su(s)- l(1)1Bk+ Df(1)yT13-464 ` 2, 4 su(s)- l(1)1Bk+ Df(1)yT14-546 2, 4 l(1)1Bk- l(1)1Ca+ Df(1)yT14-576 2, 4 l(1)1Bk- l(1)1Ca+ Df(1)yT15-5 2, 4 l(1)Ca- mul+ Df(1)yT15-6 2, 4 l(1)Ca- mul+ Df(1)yT15-28 2, 4 l(1)Ca- mul+ Df(1)yT15-56 2, 4 l(1)Ca- mul+ Df(1)yT15-105 2, 4 l(1)Ca- mul+ Df(1)yT15-158b 2, 4 l(1)Ca- mul+ Df(1)yT15-161 2, 4 l(1)Ca- mul+ Df(1)yT15-171 2, 4 l(1)Ca- mul+ Df(1)yT15-177 2, 4 l(1)Ca- mul+ Df(1)yT15-183 2, 4 l(1)Ca- mul+ Df(1)yT15-189 2, 4 l(1)Ca- mul+ Df(1)yT15-219 2, 4 l(1)Ca- mul+ Df(1)yT15-222 2, 4 l(1)Ca- mul+ Df(1)yT15-270 2, 4 l(1)Ca- mul+ Df(1)yT15-274 2, 4 l(1)Ca- mul+ Df(1)yT15-286 2, 4 l(1)Ca- mul+ Df(1)yT15-300 2, 4 l(1)Ca- mul+ Df(1)yT15-318 2, 4 l(1)Ca- mul+ Df(1)yT15-325 2, 4 l(1)Ca- mul+ Df(1)yT15-327 2, 4 l(1)Ca- mul+ Df(1)yT15-334 2, 4 l(1)Ca- mul+ Df(1)yT15-364 2, 4 l(1)Ca- mul+ Df(1)yT15-365 2, 4 l(1)Ca- mul+ Df(1)yT15-383 2, 4 l(1)Ca- mul+ Df(1)yT15-390 2, 4 l(1)Ca- mul+ Df(1)yT15-392 2, 4 l(1)Ca- mul+ Df(1)yT15-405 2, 4 l(1)Ca- mul+ Df(1)yT15-408 2, 4 l(1)Ca- mul+ Df(1)yT15-410 2, 4 l(1)Ca- mul+ Df(1)yT15-412 2, 4 l(1)Ca- mul+ Df(1)yT15-433 2, 4 l(1)Ca- mul+ Df(1)yT15-449 2, 4 l(1)Ca- mul+ Df(1)yT15-460 2, 4 l(1)Ca- mul+ Df(1)yT15-468 2, 4 l(1)Ca- mul+ Df(1)yT15-502 2, 4 l(1)Ca- mul+ Df(1)yT15-509 2, 4 l(1)Ca- mul+ Df(1)yT15-511 2, 4 l(1)Ca- mul+ Df(1)yT15-517 2, 4 l(1)Ca- mul+ Df(1)yT15-533 2, 4 l(1)Ca- mul+ Df(1)yT15-543 2, 4 l(1)Ca- mul+ Df(1)yT15-548 2, 4 l(1)Ca- mul+ Df(1)yT15-552 2, 4 l(1)Ca- mul+ Df(1)yT15-564 2, 4 l(1)Ca- mul+ Df(1)yT15-568 2, 4 l(1)Ca- mul+ Df(1)yT15-575 2, 4 l(1)Ca- mul+ Df(1)yT15-586 2, 4 l(1)Ca- mul+ Df(1)yT15-597 2, 4 l(1)Ca- mul+ Df(1)yT15-599 2, 4 l(1)Ca- mul+ Df(1)yT16-14 2, 4 mul- tw+ Df(1)yT16-411 2, 4 mul- tw+ Df(1)yT16-499 2, 4 mul- tw+ Df(1)yT16-534 2, 4 mul- tw+ Df(1)yT16-554 2, 4 mul- tw+ Df(1)yT17-570 2, 4 tw- l(1)1Da+ Df(1)yT17-600 2, 4 tw- l(1)1Da+ Df(1)yT18-319 2, 4 l(1)Da- brc+ Df(1)yT19-16 2, 4 brc- l(1)1Dc+ Df(1)yT19-253 2, 4 brc- l(1)1Dc+ ( The number preceeding the hyphen designates the intergenic interval in which the break has occurred, and the numbers following the hyphen represent independent occurrences. | 1 = Campos, Grossman, and White, 1985, J. Neurogenet. 2: 197-218; 2 = Mason, Voelker, Rosen, Campos, White, and Lim, 1986, DIS 63: 164-65; 3 = Ruiz-Gomez and Modolell, 1988, Genes Dev. 1: 1238-46; 4 = Voelker. / DNA coordinates from Caramolino, Ruiz-Gomez, Guerrero, Cam- puzano, and Modolell, 1982, EMBO J. 1: 1185-91 and Cam- puzano, Carramolino, Cabrera; Ruiz-Gomez, Villares, Boronat, and Modolell, 1985, Cell 40: 3227-38. Origin (coordinate 0) is the distal EcoR1 site within the scS2 molecular defi- ciency ("+" values to the left, "-" values to the right). Df(1)yT2-623 and Df(1)yT2-696 have multiple breakpoints. The unstable chromosome ends lose approximately 75 base pairs per generation (Biessman and Mason, 1988, EMBO J. 7: 1081-86). The presented data represent the extents of the deficiencies as of 1985. ` Broken within su(s). # In(1)z+: Inversion (1) zeste wild origin: X ray induced. Recovered as z reversion in genotype ordinarily exhibiting z phenotype. inversion cytology ref ( ___________________________________________ In(1)z+1 3C1;3F5-6 1 In(1)z+2 3C1-2;7A 1 In(1)z+7G3 3C3-5;14B4-C1;20A3 2 In(1)z+8 3C1-3;20D-F 1 In(1)z+11E7 3C2-5;17C4-D1;20A3 2 In(1)z+28 2B-C;3C 1 In(1)z+30 3C1-2;5D 1 In(1)z+38 3C;10C-D 1 In(1)z+48 3C1-2;4D-5D 1 In(1)z+50 3C1-2;20B-C 1 In(1)z+51 1F3-4;3B4-C1;12B-D;20 1 ( 1 = Gelbart, 1971, Ph.D. Thesis, Univ. of Wisconsin; 2 = Gans, 1953, Bull. Biol. Fr. Belg., Suppl. 38: 1-90. # Df(1)ZWD5 cytology: Band at 3C in Df(1)ZWD5/+ salivaries wedge-shaped indicating small deficiency. origin: Irradiation of z1 males. references: Smolik-Utlaut and Gelbart, 1987, Genetics 116: 285-98. genetics: Homozygous lethal. Notch wing in Df(1)ZWD5/+. # Df(Y)bb: see Ybb- # Df(YL) and Df(YS) origin: X ray or / ray induced in BSYy+ (Lindsley et al, 1972; Hazelrigg et al, 1982) or y+Y (Brosseau, 1960); / ray induced in y+Y (Schwartz). genetics: Recovered as male-sterile Y chromosomes; presence of deficiencies established by cytological examination of pro- phase and metaphase figures. Missing fertility factors in deficiencies of Brosseau, Hazelrigg et al., and Schwartz indi- cated. deficiency cytology ( ref | genetics _______________________________________________________________ Df(YL)A5 3 kl-3- kl-2+ kl-1- Df(YL)A10 3 kl-3--kl-1- Df(YL)A11 3 BS- kl-5--kl-3- Df(YL)A17 3 kl-3--kl-1- Df(YL)A29 / 3 kl-3- Df(YL)A32 3 kl-5--kl-3- Df(YL)A33 / Df(YL)A39 3 kl-5--kl-3- Df(YL)A49 ` 3 kl-3--kl-2- Df(YL)A78 BSXh;h10;87B 2, 5 Df(YL)A80 BSXh;h7 + h21;35B 2, 5 Df(YL)A109 BSXh;h13;83E 2, 5 Df(YL)A111 h5;h11 + h14;28D 2, 5 Df(YL)A158 h3;h14;63A 2, 5 Df(YL)B2 - h3;h8 1, 2 kl-5--kl-3- Df(YL)B4 3 kl-5--kl-3- Df(YL)B12 3 BS-kl-5--kl-3- Df(YL)B14 3 kl-5--kl1- Df(YL)B172 BSXh;h3;95A 2, 5 Df(YL)B225 h3;h10 + BSXh;73D 2, 5 Df(YL)B236 BSXh;h16;25D-E 2, 5 Df(YL)D211 BSXhj;h3;26A 2, 5 Df(YL)G8 h3;h8;85F 2, 5 Df(YL)G18 4 kl-5--kl-1- Df(YL)G19 4 kl-3--kl-2- Df(YL)G20 4 kl-3--kl-2- Df(YL)G21 4 kl-5--kl-2- Df(YL)G22 4 kl-5--kl-2- Df(YL)G23 4 kl-5--kl-2- Df(YL)G24 4 kl-5--kl-2- Df(YL)G26 4 kl-5--kl-3- Df(YL)G27 4 kl-5--kl-3- Df(YL)G28 4 kl-5--kl-3- Df(YL)G29 4 kl-5--kl-3- Df(YL)G30 4 kl-5--kl-3- Df(YL)G48 h3;h7 + Xhy+;88C 2, 5 Df(YL)H52 h3;h16 + Xhy+;27E 2, 5 Df(YL)H121 h3;h13 + h16;26B 2, 5 Df(YL)H143 BSXh;h14;59F 2, 5 Df(YL)J59 h3;h16 + Xhy+;43A 2, 5 Df(YL)J96 BSXh;h8 + h16;25A 2, 5 Df(YL)J112 BSXhj;h3 + h25D;71B-C 2, 5 Df(YL)J118 h3;h10 + h21;22D 2, 5 Df(YL)J136 h3;h9 + BSXh;26F 2, 5 Df(YL)J154 h1-2;h3 + h25D;63A 2, 5 Df(YL)L132 BSXh;h16 + Xhy+;83C-D 2, 5 Df(YL)R136 h3;h7;22D 2, 5 Df(YL)R158 BSXhj;h10 + Xhy+;32F 2, 5 Df(YL)S5 h13;h14-15 2 kl-1- Df(YL)S6 h13;h17 2 kl-1- Df(YL)S7 h3;h8-9 2 kl-5--kl-3- Df(YL)S8 y+Xh;h8 2 kl-5--kl-3- Df(YL)S9 h3;h11 2 kl-5--kl-2- Df(YL)S10 y+Xh;h11 2 kl-5--kl-2- Df(YL)S11 h3;h11 2 kl-5--kl-2- Df(YL)S13 / h3;h9 2 kl-5--kl-3- Df(YL)S14 / y+Xh;h14 2 kl-5--kl-1- Df(YL)S21 y+Xh;h2 2 kl-5- Df(YS)A6 3 ks-1--ks-2- Df(YS)A29 / 3 ks-1- Df(YS)A33 / 3 ks-1- Df(YS)B4 h21;h25 1, 2 ks-1--ks-2- Df(YS)B13 n 3 ks-1--ks-2- Df(YS)G4 4 ks-1--ks-2- Df(YS)G5 4 ks-1--ks-2- Df(YS)S12 h18;h25 2 ks-1--ks-2- Df(YS)S13 / h22;h25 2 ks-1--ks-2- Df(YS)S14 / h19;h25 2 ks-1--ks2- ( Many Y deficiencies are also Y-autosome translocations. Three-break translocations that have lost a segment between two Y chromosome breakpoints are listed with three break- points, the last one being the autosomal breakpoint of the translocation (for example, Df(YL)A78=BSXh;h10;87B), whereas deficiencies that are independent of the Y-autosome- translocation breakpoints are listed with two deficiency breakpoints plus two translocation breakpoints when known (for example, Df(YL)A80=BSXh;h7 + h21;35B. New orders of these rearrangements are provided with description of the like-designated Y-autosome translocations. Deficiencies unassociated with translocations are listed with two break- points (for example, Df(YL)B2=h3;h8). | 1 = Brosseau, 1960, Genetics 45: 257-74; 2 = Gatti and Pim- pinelli, 1983, Chromosoma 83: 349-73; 3 = Hazelrigg, For- nili, and Kaufman, 1982, Chromosoma 87: 535-59; 4 = Kennison; 5 = Lindsley, Sandler, Baker, Carpenter, Denell, Hall, Jacobs, Miklos, Davis, Gethman, Hardy, Hessler, Miller, Nozawa, Parry, and Gould-Somero, 1972, Genetics 71: 157-84. / Occurs in chromosome carrying two noncontiguous deletions, one in YL and the other in YS (for example, Df(YL)A29 and Df(YS)A29). ` Also see In(YLS)A49. - Also see In(YL)B2. Also see T(Y;3)S21. n Also see T(Y;2)B13. # Df(YS)bb: see Ybb-