Variation Information: q89

Nameq89 View on WormBase
Species C. elegans
Genetic positionII:1.67 +/- 0.000 cM
Genomic positionII: 9714506..9714506
Protein changeY53C12A.1 Substitution

Strains carrying this variation

Strain Genotype Species Description
SL940 wee-1.3(q89eb94) unc-4(e120)/mIn1 [dpy-10(e128) mIs14] II. C. elegans Heterozygotes are WT with major GFP signal in pharynx. Segregates Dpy GFP+ mIn1 homozygotes and GFP- Uncs which are viable but lay oocytes (lay viable embryos if mated to WT males). Strain has a Him phenotype. 3.4% males. Mutant males have abnormal sperm. Class 1 suppressor.
SL978 wee-1.3(q89eb60) unc-4(e120)/mIn1 [dpy-10(e128) mIs14] II. C. elegans Heterozygotes are WT with major GFP signal in pharynx. Segregates Dpy GFP+ mIn1 homozygotes and GFP- Uncs which are viable but lay inviable embryos (lay viable embyros if mated to WT males). Strain has a Him phenotype. 0.4% males. Mutant males are fertile. Class 2 suppressor.