Variation Information: e1926

Namee1926 View on WormBase
Species C. elegans
Genetic positionX:-16.05 +/- 0.091 cM
Genomic positiongenomic coordinates unknown or not listed
Protein changeprotein change unknown or not listed

Strains carrying this variation

Strain Genotype Species Description
CB4377 lin-22(n372) pal-2(e2260) IV; him-5(e1490) V; lin-32(e1926) X. C. elegans Hermaphrodites segregating males with abnormal ray lineages. Reference: Hodgkin et al. (1989) Genome, 31, 625-637. doi:10.1139/g89-116.
EM496 hlh-2(bx108) I; him-5(e1490) V; lin-32(e1926) X. C. elegans Males are rayless. hlh-2(bx108) strongly and semi-dominantly enhances the ray-loss phenotype of lin-32(e1926).