[53D14-53D14];[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.
53D14;53F8
Lethal in combination with Df(2R)BSC359.
Inferred to overlap with: Df(2R)BSC359.
Inferred to overlap with: Df(2R)BSC331.
Heterozygotes show resistance to halothane and hypersensitivity to enflurane compared to controls.
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{EP}BEST:SD02913EP2148&P{lacW}Dekk09907 and P{lacW}CG6426k10209&P{lacW}vegk07202 Limits of break 2 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