[53E4-53E4];[53F8-53F8];
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.
53E4;53F8
Inferred to overlap with: Df(2R)P803-Delta15.
Lethal in combination with Df(2R)P803-Δ15.
Lethal in combination with In(2LR)DTD99. Lethal in combination with Df(2R)P803-Δ15.
Heterozygotes show resistance to halothane compared to controls.
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 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}l(2)k11405k11405&P{EP}EP641 and P{lacW}l(2)k10815k10815