Variation Information: tm1833

Nametm1833 View on WormBase
Species C. elegans
Genetic positionV:3.98 +/- 0.003 cM
Genomic positionV: 12271818..12272675
Protein changeF55C5.4 Deletion

Strains carrying this variation

Strain Genotype Species Description
KIR2 capg-2(tm1833) V/nT1 [qIs51] (IV;V). C. elegans Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested nT1[qIs51] aneuploids, and non-GFP capg-2 homozygotes (sick, sterile, Unc). Homozygous nT1[qIs51] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. Reference: Csankovszki G, et al., Curr Biol. 2009 Jan 13;19(1):9-19.