Variation Information: gk522

Namegk522 View on WormBase
Species C. elegans
Genetic positionII:-0.86 +/- 0.000 cM
Genomic positionII: 5890674..5891241
Protein changeF55C12.1a F55C12.1a F55C12.1a F55C12.1b F55C12.1c F55C12.1d Deletion

Strains carrying this variation

Strain Genotype Species Description
VC1082 F55C12.1a(gk522)/mIn1 [mIs14 dpy-10(e128)] II. C. elegans F55C12.1a. Homozygous lethal deletion chromosome balanced by GFP- and dpy-10-marked inversion. Heterozygotes are WT with relatively dim pharyngeal GFP signal, and segregate WT dim GFP, Dpy bright GFP (mIn1 homozygotes), and non-GFP gk522 homozygotes (early larval arrest). Pick WT dim GFP and check for correct segregation of progeny to maintain. Attribution: This strain was provided by the C. elegans Reverse Genetics Core Facility at the University of British Columbia, which is part of the international C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use. Paper_evidence WBPaper00041807