Gene Information: lin-32

Namelin-32 View on WormBase
Species C. elegans
SequenceT14F9.5
Genetic positionX:-16.05 +/- 0.091 cM
Genomic positionX: 2229055..2230122

Strains carrying this gene

Strain Genotype Description
CB4377 lin-22(n372) pal-2(e2260) IV; him-5(e1490) V; lin-32(e1926) X. Hermaphrodites segregating males with abnormal ray lineages. Reference: Hodgkin et al. (1989) Genome, 31, 625-637. doi:10.1139/g89-116.
EM172 unc-4(e120) II; him-5(e1490) V; lin-32(bx46) X. Missing Rays. Unc.
EM496 hlh-2(bx108) I; him-5(e1490) V; lin-32(e1926) X. Males are rayless. hlh-2(bx108) strongly and semi-dominantly enhances the ray-loss phenotype of lin-32(e1926).
OH4226 vtIs1 V; lin-32(ot259) X. vtIs1 [dat-1p::GFP + rol-6(su1006)] V. Rollers. Fewer or extra cells expressing dat-1::GFP in various penetrances.
OH4335 vtIs1 V; lin-32(ot297) X. vtIs1 [dat-1p::GFP + rol-6(su1006)] V. Rollers. Missing CEPVs and PDEs; ADEs variably affected.
OH6072 vtIs1 vsIs33 V; lin-32(ot338) X. vtIs1 [dat-1p::GFP + rol-6(su1006)] V. vsIs33 [dop-3::RFP] V. Missing CEPVs and PDEs; ADEs variably affected.
OH7008 vtIs1 vsIs33 V; lin-32(ot343) X. vtIs1 [dat-1p::GFP + rol-6(su1006)] V. vsIs33 [dop-3::RFP] V. Rollers. Fewer or extra cells expressing dat-1::GFP in various penetrances.
OH7118 vtIs1 vsIs33 V; lin-32(ot366) X. vtIs1 [dat-1p::GFP + rol-6(su1006)] V. vsIs33 [dop-3::RFP] V. Missing CEPVs and PDEs; ADEs variably affected.
TU282 lin-32(u282) X. Touch insensitive in tail.