Variation Information: n1790
| Name | n1790 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | IV:-8.49 +/- 0.000 cM |
| Genomic position | IV: 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. |