Variation Information: n767

Namen767 View on WormBase
Species C. elegans
Genetic positionX:22.95 +/- 0.000 cM
Genomic positionX: 15734038..15734215
Protein changeZK678.1 Deletion

Strains carrying this variation

Strain Genotype Species Description
MT10408 lin-53(n833) I; unc-76(e911) V; lin-15A(n767) X; nEx998. C. elegans nEx998 [lin-53::GFP + unc-76(+)]. Pick non-Unc, non-Muv to maintain.
MT12719 lin-61(n3809) I; lin-15A(n767) X. C. elegans Reference: Andersen EC, et al. Genetics. 2008 Aug;179(4):2001-12. Harrison MM, et al. Genetics. 2007 May;176(1):255-71.
MT15537 unc-30(e191) lin-54(n3423) IV/nT1 [qIs51] (IV;V); lin-15A(n767) X. C. elegans Heterozygotes are Muv and GFP+ and segregate SteUncMuv GFP- and dead eggs. n3423 is PVul and sterile when alone; Muv in synMuv class A background.
MT16429 set-6(tm1611) lin-15A(n767) X. C. elegans Reference: Andersen EC & Horvitz HR., Development. 2007 Aug;134(16):2991-9.
MT1643 lin-36(n766) III; lin-15A(n767) X. C. elegans Double mutant is Muv. lin-36 alone is non-Muv.
MT16529 lin-61(n3447) I; lin-15A(n767) X. C. elegans SynMuv B. Reference: Andersen EC, et al. Genetics. 2008 Aug;179(4):2001-12. Harrison MM, et al. Genetics. 2007 May;176(1):255-71.
MT1806 lin-15A(n767) X. C. elegans WT phenotype. Synthetic Muv.
MT5828 lin-36(n766) unc-36(e251) III; lin-15A(n767) X. C. elegans Unc. Muv.
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.