Variation Information: n766

Namen766 View on WormBase
Species C. elegans
Genetic positionIII:-0.45 +/- 0.000 cM
Genomic positionIII: 8017886..8017886
Protein changeF44B9.6 Substitution

Strains carrying this variation

Strain Genotype Species Description
MT1643 lin-36(n766) III; lin-15A(n767) X. C. elegans Double mutant is Muv. lin-36 alone is non-Muv.
MT1799 lin-36(n766) unc-32(e189) III. C. elegans Unc.
MT5828 lin-36(n766) unc-36(e251) III; lin-15A(n767) X. C. elegans Unc. Muv.
MT6034 lin-36(n766) III. C. elegans WT. Synthetic Muv with lin-8, lin-38 or lin-15(n767).
MT9343 lin-36(n766) III; lin-15A(n767) X; nIs93. C. elegans nIs93 [(pJHT27)lin-36p::GFP::lin-36 (full-length coding) + rol-6(su1006)]. Rollers. Non-Muv -- nearly completely penetrant rescue of Lin-36. Reference: Thomas & Horvitz (1999) Development 126(15):3449-59.