Variation Information: tm2639

Nametm2639 View on WormBase
Species C. elegans
Genetic positionII:0.75 +/- 0.001 cM
Genomic positionII: 8183841..8184651
Protein changeT05C12.6a T05C12.6b T05C12.6c Deletion

Strains carrying this variation

Strain Genotype Species Description
HS1795 dsh-2(or302) mig-5(tm2639)/mIn1 [dpy-10(e128) mIs14] II. C. elegans Heterozygotes are WT with pharyngeal GFP. Segregates WT GFP+, Dpy GFP+ (mIn1 homozygotes) and few GFP- dsh-2(or302) mig-5(tm2639) homozygotes (Sys). Pick WT GFP+ animals and check for correct segregation of progeny to maintain.
HS2725 dsh-2(or302) dsh-1(ok1445) mig-5(tm2639)/mIn1 [dpy-10(e128) mIs14] II. C. elegans Heterozygotes are WT with pharyngeal GFP. Segregates WT GFP+, Dpy GFP+ (mIn1 homozygotes) and non-GFP triple homozygotes (mostly Emb with a few animals surviving to early L1). Pick WT GFP+ animals and check for correct segregation of progeny to maintain.
HS2728 dsh-1(ok1445) mig-5(tm2639) II. C. elegans One or no gonad arm. Frequently ruptures at vulva.