Variation Information: n1792

Namen1792 View on WormBase
Species C. elegans
Genetic positionI:-1.72 +/- 0.000 cM
Genomic positionI: 4127063..4127063
Protein changeE01A2.3 Substitution

Strains carrying this variation

Strain Genotype Species Description
EW52 lin-44(n1792) I; cwn-2(ok895) IV. C. elegans
EW53 lin-44(n1792) I; cwn-1(ok546) II; cwn-2(ok895) IV. C. elegans
EW68 lin-44(n1792) I; cwn-1(ok546) II. C. elegans
EW77 lin-44(n1792) I; egl-20(n585) IV/nT1 [qIs51] (IV;V); dpy-11(e1180) mom-2(or42) V/nT1 [qIs51] (IV;V). C. elegans
HS1680 lin-44(n1792) zdIs5 I; cwn-1(ok546) II; egl-20(n585) cwn-2(ok895) IV/nT1 [qIs51] (IV;V); mom-2(ne874) V/nT1. C. elegans zdIs5 [mec-4p::GFP + lin-15(+)] I. Homozygous nT1[qIs51] are inviable. mec-4::GFP is expressed in touch neurons. Heterozygotes are strong Egl Psa GFP+ and segregate dead eggs and non-GFP Unc Egl Psa that give only dead eggs at 25C.
KS46 lin-44(n1792) I; egl-20(n585) IV. C. elegans
MT4051 lin-44(n1792) I; him-5(e1490) V. C. elegans At 20C about 50% of the hermaphrodites are Egl. Males have an abnormal tail and do not mate.
MT4705 lin-17(n671) lin-44(n1792) I; him-5(e1490) V. C. elegans
MT5383 lin-44(n1792) I. C. elegans At 20C about 50% of the hermaphrodites are Egl.