[49C3-49C3];[49E7-49E7];
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.
49C3;49E7
Lethal in combination with Df(2R)Exel8056.
Heterozygotes show hypersensitivity to halothane and enflurane 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.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}Nacα04329 and P{lacW}bick10712 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}Psck07834&P{lacW}Su(z)2k06344 and P{EP}EP873EP873