Variation Information: ok1066

Nameok1066 View on WormBase
Species C. elegans
Genetic positionIII:-0.88 +/- 0.004 cM
Genomic positionIII: 6937058..6937765
Protein changeF57B9.4a F57B9.4e Deletion

Strains carrying this variation

Strain Genotype Species Description
VC752 coq-2(ok1066) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans F57B9.4a. Homozygous viable deletion chromosome balanced by bli-4- and GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP ok1066 homozygotes (viable lethargic Unc, various body morphology defects, often grotty, does not starve plate easily). Homozygous hT2[bli-4 let-? qIs48] inviable. Note: qIs48 has been observed to recombine off hT2, typically leaving behind a functional homozygous viable hT2 with Bli-4 phenotype. Pick WT 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