Variation Information: n1790

Namen1790 View on WormBase
Species C. elegans
Genetic positionIV:-8.49 +/- 0.000 cM
Genomic positionIV: 2277275..2277275
Protein change Substitution

Strains carrying this variation

Strain Genotype Species Description
WU125 lin-1(n1790) IV. C. elegans n1790 causes a partially penetrant "rod-like" larval lethal phenotype (17% at 20C) and a partially penetrant vulvaless defect (50% at 20C). A Smg mutation enhances these phenotypes. The n1790 mutation is a nonsense change at codon 352.