[7F7-7F7];[8B4-8B4];
A set of ~800 largely isogenic deficiency stocks created by FLP-induced recombination between FRT-carrying transgenic insertions; molecularly defined deletion endpoints correspond to initial location of the progenitor insertions. Designed to fill gaps in deletion coverage and breakpoint placement; also used to replace older available deficiencies that have not been molecularly mapped.
7F7;8B4
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Df(1)BSC592/Df(1)BSC627 embryos display axon guidance defects.
Inferred to overlap with: Df(1)BSC592.
1: PBac{WH}CG12659f07899
2: P{XP}CG12075d09295
Homozygous Df(1)BSC627 embryos display axon guidance defects in which axons appear to circle the midline.
The presence of P+PBac{XP5.WH5}BSC627 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(1)BSC627 predicted from the Release 5 genomic coordinates of the insertions sites of the progenitor PBac{WH}CG12659f07899 and P{XP}CG12075d09295 transposable elements are 7F7;8B4.