Variation Information: rh147

Namerh147 View on WormBase
Species C. elegans
Genetic positionII:0.75 +/- 0.000 cM
Genomic positionII: 8183750..8183750
Protein changeT05C12.6a T05C12.6b T05C12.6c Substitution

Strains carrying this variation

Strain Genotype Species Description
SU352 mig-5(rh147)/mIn1 [dpy-10(e128) mIs14] II. C. elegans Heterozygotes are WT with GFP in pharynx. Segregate Dpy and GFP+. mig-5 homozygotes are non-GFP and show a weakly penetrant gonad defect and a fully penetrant QL.d migration defect.