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.
Genomic location indicated corresponds to first base of unique genomic sequence (coordinate 132 in CZ474635).
Genomic location previously reported as X:1268453..1268453 .
A P{XP} element is inserted in the opus transposon.
Location X:1231240-1231241 determined by FlyBase alignment of dbGSS accession CZ474635 to D. melanogaster arm Release_4 and heterochromatin Release_3.2b. Insertion orientation revised.
Accession CZ474635: initial 132nt consists of unique sequence.