[49C2-49C2];[49E1-49E1];
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 set of 519 isogenic deletions provides 56% genome coverage.
The current Exelixis collection at the Bloomington Stock Center differs from the original described in FBrf0175003 : a significant number were shown not to carry a deletion and have been removed from the collection; a number of stocks have been lost; a number of additional deletions are included that were generated after publication.
49C2;49E1
Breakpoint from FlyBase's release 5 sequence location of progenitor insertion.
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Df(2R)Exel8056/Df(2R)vg-D transheterozygosity is lethal.
Lethal in combination with Df(2R)ED2308.
Df(2R)Exel8056 homozygosity is lethal.
Heterozygotes show hypersensitivity to halothane compared to controls.
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}AmphEP2175/P{lacW}spt4k05316 and P{PZ}ox1 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}bick10712 and P{PZ}l(2)0142401424