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 < 100 bp) to the right (centromere-proximal) of 2L:9908615 (release 6), either within the annotated CG13124 transcription unit or just upstream of its 5' end.
7.303
d10773
Exelixis, Inc. determined the insertion site of P{XP}CG13124d10773 to be at Release 3 genomic coordinate 9900868, which is predicted to lie in 30E3 on the Release 3 map and 30E1 on the Release 4 map.