Variation Information: ok1588

Nameok1588 View on WormBase
Species C. elegans
Genetic positionIV:3.71 +/- 0.001 cM
Genomic positionIV: 8304223..8306197
Protein changeF35H10.4 F35H10.4 F35H10.4 Deletion

Strains carrying this variation

Strain Genotype Species Description
VC1148 vha-5(ok1588) IV/nT1 [qIs51] (IV;V). C. elegans F35H10.4. Homozygous lethal deletion chromosome balanced by GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested nT1[qIs51] aneuploids, and non-GFP ok1588 homozygotes (arrest stage/phenotype undetermined). Homozygous nT1[qIs51] inviable. 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