Variation Information: ma164

Namema164 View on WormBase
Species C. elegans
Genetic positionV:4.77 +/- 0.000 cM
Genomic positionV: 12969889..12969889
Protein changeR186.4 Substitution

Strains carrying this variation

Strain Genotype Species Description
VT1102 lin-28(n719) I; lin-46(ma164) nDf51 V; mir-84(n4037) X. C. elegans Strong retarded heterochronic phenotype, reiteration of L2-stage program resulting in extra seam cells and failure to generate alae. nDf51 is a 5930 bp deletion starting 1762 bp upstream of mir-241, removing mir-241, mir-48, and F56A12.6 (snoRNA).
VT1145 lin-46(ma164) nDf51 V; mir-84(n4037) X. C. elegans Strong retarded heterochronic phenotype, reiteration of L2-stage program resulting in extra seam cells and failure to generate alae. Vul. nDf51 is a 5930 bp deletion starting 1762 bp upstream of mir-241, removing mir-241, mir-48, and F56A12.6 (snoRNA).
VT581 dpy-5(e61) lin-28(n719) I; lin-46(ma164) unc-76(e911) V. C. elegans Dpy Unc. Egl+. lin-46 suppresses precocious Egl- phenotype of lin-28. lin-46 alone makes gaps in adult alae; enhanced at 15C.