Variation Information: ok1681

Nameok1681 View on WormBase
Species C. elegans
Genetic positionIV:0.31 +/- 0.015 cM
Genomic positionIV: 4448025..4449176
Protein changeR08C7.2a R08C7.2c R08C7.2d Deletion

Strains carrying this variation

Strain Genotype Species Description
VC1258 R08C7.2(ok1681) IV/nT1 [qIs51] (IV;V). C. elegans R08C7.2. Homozygous sterile 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 ok1681 homozygotes (sterile, lays eggs that don't hatch). Homozygous nT1[qIs51] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. External left primer: GATACTCGGCCGCTACTCAG. External right primer: TCAACGTCATTGTCACACGA. Internal left primer: ACGAACATTGGGAAAAATCG. Internal right primer: ATGAATTTCCGAGACGTTGC. Internal WT amplicon: 2519 bp. Deletion size: 1152 bp. 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