[89E11-89E11];[90C1-90C1];
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.
89E11;90C1
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Df(3R)BSC634 failed to complement Df(3R)ED5780 for lethality.
Inferred to overlap with: Df(3R)BSC634.
Inferred to overlap with: Df(3R)BSC565.
Df(3R)Exel6176 fails to complement Df(3R)ED5780.
Inferred to overlap with: Df(3R)Exel6176.
Inferred to overlap with: Df(3R)ED5794.
No cardiac or bristle phenotypes are observed in heterozygous Df(3R)ED5780 mutant females.
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.
Confirmed by PCR (using the 3-step process described on http://www.drosdel.org.uk/del_confirm.php).
Limits of break 1 computationally determined from location of progenitor P insertion on genome sequence between P{EP}CG5208EP562&P{EP}DadEP3196 and P{PZ}l(3)0788207882 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{PZ}l(3)0788207882 and P{EP}cpoEP3679