Variation Information: ok1586

Nameok1586 View on WormBase
Species C. elegans
Genetic positionI:-3.94 +/- 0.036 cM
Genomic positionI: 3289525..3291177
Protein changeW01B11.2a W01B11.2b Deletion

Strains carrying this variation

Strain Genotype Species Description
VC1167 sulp-6(ok1586) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans W01B11.2. Apparent 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 ok1586 homozygotes (probable early larval arrest). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. External left primer: TGGTTGGAACAGTTGTGGAA. External right primer: TTCATGTCTATTCGCCCACA. Internal left primer: TGGCTCAACAAATGGAACAA. Internal right primer: TTCGGTATTTCCGCATCTTC. Internal WT amplicon: 3052 bp. Deletion size: 1653 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