Variation Information: ok1398

Nameok1398 View on WormBase
Species C. elegans
Genetic positionII:1.06 +/- 0.006 cM
Genomic positionII: 9161879..9162632
Protein changeW07A12.7 Deletion

Strains carrying this variation

Strain Genotype Species Description
VC895 rhy-1(ok1398)/mIn1 [mIs14 dpy-10(e128)] II. C. elegans W07A12.7. 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 ok1398 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