Variation Information: ok2889

Nameok2889 View on WormBase
Species C. elegans
Genetic positionV:24.52 +/- 0.017 cM
Genomic positionV: 20057027..20057914
Protein changeY113G7A.6a Y113G7A.6b Y113G7A.6c Y113G7A.6d Deletion

Strains carrying this variation

Strain Genotype Species Description
VC2961 ttx-1(ok2889)/unc-51(e369) rol-9(sc148) V. C. elegans Y113G7A.6. Apparent homozygous lethal deletion chromosome balanced by flanking markers. Heterozygotes are WT and segregate WT, Unc-51 Rol-9 homozygotes and ok2889 homozygotes (arrest stage/phenotype undetermined). Pick WT and check for correct segregation of progeny to maintain. External left primer: TCTCGGGGAGTTGAATTTTG. External right primer: TTTTTCCCGAATTTTTGCAC. Internal left primer: ATGTCTTCCCGCATGAAAAT. Internal right primer: CCAGTGGTCAGAAAGCCAAT. Internal WT amplicon: 1294 bp. Deletion size: 888 bp. Deletion left flank: GTTGTTTTCTAGAAAATCTGAAAATTTTTA. Deletion right flank: TTACGAATATGAAATTTATCAAGGTCTAGG. 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