85D12;85E10
85D12;85E10
85D11;85E10
85D11-85D13;85E10
bk1 << l(3)85Db << Scm << bk2 << MtnA
Breakpoint(s) molecularly mapped
Df(3R)GB104 mutant embryos exhibit frequent breaks and/or gaps in the dorsal trunk, often associated with shorter ventral tracheal branches. Individual salivary ducts often have significant gaps or are completely missing.
In homozygous Df(3R)GB104 embryos the salivary gland fails to migrate posteriorly by stage 14.
The Df(3R)GB104 chromosome does not act as a dominant suppressor of telomeric silencing (assayed using the effect of the chromosome on the eye colour phenotype of flies carrying "P{wvar}KR3-2", a stable "brown-red" variant of the P{3'WP-2,wvar}2Lt insertion).
Dominantly enhances the KrIf-1/+ eye phenotype.
Shows a dose-sensitive interaction with pbhs.PB.
Dominantly causes tergite defects in less than 50% of run3 heterozygotes.
Heterozygosity for this deletion has no effect on the mutant ovarian phenotype of ovoD2.
Embryonic lethal.
Ref: FBrf0066905.
All limits from polytene analysis (FBrf0080317)