Variation Information: ok1547

Nameok1547 View on WormBase
Species C. elegans
Genetic positionV:6.26 +/- 0.000 cM
Genomic positionV: 14357232..14357682
Protein changeY49A3A.4 Deletion

Strains carrying this variation

Strain Genotype Species Description
VC1103 Y49A3A.4(ok1547) V/nT1 [qIs51] (IV;V). C. elegans Y49A3A.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 ok1547 homozygotes (early larval arrest). Lethal phenotype is suspicious, as deletion appears to affect only intron sequence. 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