Variation Information: n1760

Namen1760 View on WormBase
Species C. elegans
Genetic positionIII:-0.68 +/- 0.000 cM
Genomic positionIII: 7529783..7529783
Protein changeC07H6.7 C07H6.7 Substitution

Strains carrying this variation

Strain Genotype Species Description
CF439 lin-39(n1760) III; dpy-20(e1282) IV; him-5(e1490) V; muIs23. C. elegans muIs23 [hsp::lin-39 + (pMH86) dpy-20(+)]. Heat-shock inducible lin-39. muIs23 is a spontaneous integrant whose chromosomal location is unknown.
MT4007 lin-39(n1760) III. C. elegans Vulvaless. Strong loss of function allele.
MT4009 lin-39(n1760)/dpy-17(e164) unc-32(e189) III. C. elegans Heterozygotes are WT and segregate WT, DpyUnc and Vul. Pick WT to maintain.
MT7236 lin-39(n1760) egl-5(n945) III. C. elegans n1760: strong allele of lin-39, vulvaless (n300-like). n945: HSN-. Egl. Coiler.
MT7238 sma-3(e491) mab-5(e1239) egl-5(n945)/lin-39(n1760) mab-5(e1239) egl-5(n945) III. C. elegans
MT7255 lin-39(n1760) mab-5(e1239) egl-5(n945) III. C. elegans Small brood size. Semi-sterile. n945: HSN-. Egl. Coiler.
MT7419 lin-39(n1760) mab-5(e1239)/sma-3(e491) mab-5(e1239) III. C. elegans
MT7594 lin-39(n1760) ncl-1(e1865) unc-36(e251) III; sDp3 (III;f). C. elegans Pick WT to maintain strain. Dp lost at high frequency, usable for mosaic analysis. Animals without the Dp are Unc, Vul and Ncl.