[87C7-87C7];[87F6-87F6];
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.
87C7;87F6
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
No cardiac or bristle phenotypes are observed in heterozygous Df(3R)ED5612 mutant females.
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}Vha55j2E9 and P{PZ}CtBP03463 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}CtBP03463 and P{lacW}B52s2249&P{lacW}flflL4179