[52D11-52D11];[52E7-52E7];
A set of 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. Initial core set of 209 isogenic deletions provides ~60% euchromatic genome coverage.
52D11;52E7
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Lethal in combination with Df(2R)BSC888.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Confirmed by 3-step PCR confirmation as shown in http://www.drosdel.org.uk/del_confirm.php Confirmed by lack of complementation to a known lethal mutation predicted to fall between the progenitor insertions.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k02205k02205&P{PZ}sli05248 and P{lacW}ATPCLk09217 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}spinEP645&P{lacW}spink09905 and P{lacW}Lis-1k11702&P{EP}CG8443EP969