[69C2-69C2];[69F5-69F5];
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.
69C2;69F5
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(3L)ED4483.
Inferred to overlap with: Df(3L)BSC613.
Df(3L)BSC413 mutant clones in sensory neurons in adult wing do not display any defects in injury-induced axon degeneration (following an axotomy, the severed axons are cleared away normally).
The presence of P+PBac{XP5.WH5}BSC413 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(3L)BSC413 predicted from the Release 5 genomic coordinates of the progenitor P{XP}d01629 and PBac{WH}MICAL-likef05713 insertion sites are 69C2;69F5.