Variation Information: tn1231

Nametn1231 View on WormBase
Species C. elegans
Genetic positionV:3.32 +/- 0.000 cM
Genomic positionV: 11734436..11734436
Protein changeB0240.2 Substitution

Strains carrying this variation

Strain Genotype Species Description
SL1138 spe-42(tn1231) V/nT1 [unc-?(n754) let-? qIs50] (IV;V). C. elegans Heterozygotes are Unc and express myo-2::GFP in the pharynx. spe-42(tn1231) homozygotes are non-Unc and non-GFP. spe-42(tn1231) produces <1 self progeny at 16C and no self progeny at 25C. The Spe defect can be rescued by WT sperm. Homozygous nT1[unc-?(n754) let-? qIs50] are embryonic lethal.