Variation Information: tm1191

Nametm1191 View on WormBase
Species C. elegans
Genetic positionII:3.13 +/- 0.000 cM
Genomic positionII: 10883425..10883854
Protein changeF44F4.2 Deletion

Strains carrying this variation

Strain Genotype Species Description
AD226 egg-3(tm1191)/mIn1 [mIs14 dpy-10(e128)] II. C. elegans Heterozygotes are WT with relatively dim pharyngeal GFP signal, and segregate WT dim GFP+ (heterozygotes), Dpy bright GFP+ (mIn1 homozygotes), and non-GFP tm1191 homozygotes. Pick WT dim GFP and check for correct segregation of progeny to maintain.