[55B8-55B8];[55E3-55E3];
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.
55B8;55E3
Df(2R)edl-S0520/Df(2R)ED3636 transheterozygotes do not show any obvious cardioblast patterning defects in the embryo.
Inferred to overlap with: Df(2R)BSC335.
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{PZ}Hsf03091&P{EP}Dgp-1EP731 and P{PZ}sbb04525&P{EP}EP1081EP1081 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}EP437 and P{PZ}l(2)0370903709