[43A4-43A4];[43F1-43F1];
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.
43A4;43F1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Heterozygotes show resistance to halothane compared to controls.
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{lacW}vimark16722 and P{lacW}cosk16101 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CanB2EP774 and P{lacW}lin19k01207&P{lacW}rnh1k07624