[64A1-64A1];[64A7-64A7];
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.
64A1;64A7
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
Df(3L)BSC369/Df(3L)BSC368 mutant embryos show high frequency of defects in the salivary gland lumen (including variations in lumen diameter, bending/folding or occasional branching of the lumen) compared to wild-type controls.
The presence of P+PBac{XP5.WH5}BSC369 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(3L)BSC369 predicted from the Release 5 genomic coordinates of the PBac{WH}f04973a and P{XP}CG14998d02685 transposable element insertions sites are 64A1;64A7.