Variation Information: n1761

Namen1761 View on WormBase
Species C. elegans
Genetic positionIV:-8.49 +/- 0.000 cM
Genomic positionIV: 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.