Variation Information: ok881

Nameok881 View on WormBase
Species C. elegans
Genetic positionI:3.32 +/- 0.002 cM
Genomic positionI: 8929658..8930256
Protein changeF53B6.1 Deletion

Strains carrying this variation

Strain Genotype Species Description
VC634 tsp-15(ok881) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans F53B6.1. Homozygous lethal 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 ok881 homozygotes (larval arrest, lumpy body). 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