Variation Information: n1091

Namen1091 View on WormBase
Species C. elegans
Genetic positionIII:-3.25 +/- 0.000 cM
Genomic positionIII: 4278389..4278389
Protein changeR10E4.2a R10E4.2a R10E4.2a R10E4.2a R10E4.2b R10E4.2b R10E4.2c R10E4.2f R10E4.2f R10E4.2g R10E4.2g R10E4.2i R10E4.2j R10E4.2k R10E4.2l R10E4.2m R10E4.2n R10E4.2o R10E4.2q R10E4.2r Substitution

Strains carrying this variation

Strain Genotype Species Description
BW916 sup-26(n1091) III. C. elegans Superficially wild-type. Maintain under normal conditions. Reference: Manser J, et al. (2002) Genesis 34(3):184-95.
VT3077 nDf50/mIn1 [mIs14 dpy-10(e128)] II; sup-26(n1091) III; her-1(n695) V. C. elegans Pick wild-type GFP+ to maintain. Heterozygotes are WT with GFP+ pharynx, and segregate Dpy GFP+ mIn1 homozygotes, and GFP- low viability non-Egl hermaphrodites. Viability of first generation nDf50 homozygotes (GFP-) segregated from balanced heterozygotes is rescued by maternal contribution of mir-35-41 from balancer. Second generation GFP- animals are low viability. Reference: McJunkin K, Ambros V. Genes Dev. 2017 Feb 15;31(4):422-437.