[50E1-50E1];[50E6-50E6];
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.
50E1;50E6
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).
Flies heterozygous for the deletion show a Minute bristle phenotype.
Df(2R)BSC134 heterozygotes show a severe Minute phenotype from deletion of the haploinsufficient RpS23 gene.
The stock contains a second-site deletion uncovering l(2)gl.
Presence of P+PBac{XP5.WH5}BSC134 was verified using the PCR methods and primers described in FBrf0175003.
Cytological breakpoints of Df(2R)BSC134 predicted from the transposable element insertions sites using release 4 coordinates are 50E1;50E6.