Variation Information: ok487

Nameok487 View on WormBase
Species C. elegans
Genetic positionIV:14.63 +/- 0.002 cM
Genomic positionIV: 16255565..16257819
Protein changeF38C2.2 F38C2.8 Deletion

Strains carrying this variation

Strain Genotype Species Description
VC486 hlh-17(ok487) IV/nT1 [qIs51] (IV;V). C. elegans F38C2.2. Homozygous lethal deletion balanced by GFP-marked translocation. Heterozygotes are WT with GFP signal in pharynx, and segregate WT GFP, arrested nT1 aneuploids, and non-GFP ok487 homozygotes (early larval arrest). qIs51 homozygotes 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
XA6400 hlh-17(ok487) IV/nT1 [qIs51] (IV;V). C. elegans Heterozygotes are WT and GFP+ in the pharynx. ok487 homozygotes arrest as early larvae and are GFP-. qIs51 homozygotes are inviable.