[38B1-38B1];[38C2-38C2];
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.
38B1;38C2
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Inferred to overlap with: Df(2L)ED1305.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
The presence of P+PBac{XP5.WH5}BSC258 was verified using the PCR methods and primers described in FBrf0175003.
The cytological breakpoints of Df(2L)BSC258 predicted from the Release 4 genomic coordinates of the insertion sites of the progenitor PBac{WH}sNPFf06876 and P{XP}d00322 transposable element are 38B1;38C2.