[61C1-61C1];[61C3-61C3];
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.
61C1;61C3
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Inferred to overlap with: Df(3L)BSC362.
Df(3L)BSC247 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}BSC247 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(2L)BSC247 predicted from the Release 4 genomic coordinates of the transposable element insertions sites are 61C1;61C3.