Variation Information: n1091
Name | n1091 View on WormBase |
---|---|
Species | C. elegans |
Genetic position | III:-3.25 +/- 0.000 cM |
Genomic position | III: 4278389..4278389 |
Protein change | R10E4.2a 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. |