[101F1-101F1];[102A6-102A6];
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.
101F1;102A6
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Flies heterozygous for the deletion show a Minute bristle phenotype.
Df(4)ED6364 does not uncover hybrid sterility when heterozygous in males containing the D.simulans 4th chromosome introgressed into an otherwise D.melanogaster background.
Shows a Minute phenotype: this chromosome predicted to delete RpS3A.
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 computationally determined from location of progenitor P insertion on genome sequence between P{SUPor-P}KG01127&PBac{5HPw+}A173 and PBac{5HPw+}A437