Variation Information: n569

Namen569 View on WormBase
Species C. elegans
Genetic positionII:3.17 +/- 0.006 cM
Genomic positiongenomic coordinates unknown or not listed
Protein changeprotein change unknown or not listed

Strains carrying this variation

Strain Genotype Species Description
MT1580 dpy-10(e128) unc-53(n569) II. C. elegans Dpy. Egl.
ST13 klf-3(nc13)/dpy-10(e128) unc-53(n569) II; him-8(e1489) IV. C. elegans Heterozygotes are WT and segregate WT, Dpy Uncs, and animals with muscle attachment defects and ventral cord displacement and detachment. Not well balanced. klf-3 was formerly known as mua-1.
ST30 spon-1(nc30) ncIs2/dpy-10(e128) unc-53(n569) II. C. elegans ncIs2 [pH20::GFP + pBlueScript]. Heterozygotes are WT and segregate WT, DpyUnc, and animals with muscle attachment defects and ventral cord displacement and detachment which arrest in larval development. Not well balanced. Neurons visualized with ncIs2.