89A1;89B9-89B10
88F9-89A1;89B9-89B10
88F9-89A1;89B4-89B5
l(3)neo44 << bk1 << mu1 << Sap47 << bk2 << gish
Breakpoint(s) molecularly mapped Deletes entire Sb chromosome walk. Used as part of cloning strategy to jump from 88F into 89B.
Lethal with Df(3R)sbd45.
Suppressor of In(1)wm4h position-effect variegation.
Homozygous lethal.
Shows no maternal enhancement of dpphr4.
Lethal as homozygote.
Homozygous embryos are very abnormal compared to wild-type.
Heterozygosity for this deletion enhances the mutant ovarian phenotype of ovoD2.
Crossing over in X reduced in Df(3R)sbd105/+ females (Hinton, 1966, Genetics 55: 157-64); no effect on spontaneous male recombination (Lutkin and Baker, 1979, Mutat. Res. 61: 221-27)
Df(3R)sbd105 fails to complement mu21. At least one Df(3R)sbd105 chromosome carries mu2b.
Left limit of break 1 from non-inclusion of l(3)neo44 (FBrf0067338) Right limit of break 1 from inclusion of spno (FBrf0056149) Left limit of break 2 from inclusion of Sb (FBrf0031288) Right limit of break 2 from polytene analysis (FBrf0031288)