P{XP} insertion lines from Exelixis were remapped and assessed for inclusion in the Gene Disruption Project collection; flanking sequence data were submitted to GenBank.
A set of transgenic insertion stocks derived by TE mobilization using the P-element construct P{XP}. The P{XP} construct carries the w+mC mini-white marker, long (199-bp) Scer\FRT sites, and is designed to allow flexible use of Scer\UAS sites for Scer\GAL4-driven misexpression of adjacent genes. FRT sites allow Scer\FLP-mediated recombination between other FRT-containing elements, and thus can be used to generate molecularly defined deletions.
The insertion site location is not known precisely because of low quality sequence in the region of the vector-flank junction. The location is at an unknown distance (probably < 300 bp) to the right (centromere-proximal) of 3L:2192273 (release 6), upstream of the 5' end of CG5707.
The insertion site location is not precise because the readable 3' flank sequence does not extend to the vector-flank junction. The actual insertion site location is to the right of position 2192273 (release 6).
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