[94A2-94A2];[94C4-94C4];
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.
94A2;94C4
This deletion removes a single ribosomal protein-coding gene (though other genes are also removed).
Flies heterozygous for the deletion do not show a Minute bristle phenotype.
Potential deficiency; could be generated as the recombinant product between the reduced derivatives of P{RS5}5-SZ-3238 and P{RS3}CB-5827-3.
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{lacW}howj5B5&P{EP}EP738 and P{lacW}l(3)L3560L3560 Limits of break 2 computationally determined from location of progenitor P insertion on genome sequence between P{lacW}GclmL0580 and P{EP}hhEP3521