[91D4-91D4];[92A11-92A11];
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.
91D4;92A11
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)ED5938 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.
Confirmed by PCR (using the 3-step process described on http://www.drosdel.org.uk/del_confirm.php).
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}sprd05284 and P{PZ}cdi07013&P{lacW}nosj3B6 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP650 and P{PZ}l(3)1058510585