Variation Information: n1761
| Name | n1761 View on WormBase |
|---|---|
| Species | C. elegans |
| Genetic position | IV:-8.49 +/- 0.000 cM |
| Genomic position | IV: 2277191..2277191 |
| Protein change | Substitution |
Strains carrying this variation
| Strain | Genotype | Species | Description |
|---|---|---|---|
| MT7949 | lin-1(n1761) IV. | C. elegans | n1761 cuases a partially penetrant "rod-like" larval lethal phenotype (70% at 20C) and a partially penetrant vulvaless phenotype (30% at 20C). It is a splice site defect predicted to eliminate 62 amino acids at the C-terminus. |