Variation Information: tm2868

Nametm2868 View on WormBase
Species C. elegans
Genetic positionII:-2.55 +/- 0.006 cM
Genomic positionII: 5063076..5063520
Protein changeC27A2.1 Deletion

Strains carrying this variation

Strain Genotype Species Description
YE59 smc-5(tm2868)/mIn1 [mIs14 dpy-10(e128)] II. C. elegans Homozygous viable mutation balanced by GFP- and dpy-10-marked inversion. Heterozygotes are WT with relatively dim pharyngeal GFP signal, and segregate WT dim GFP, Dpy bright GFP (mIn1 homozygotes), and non-GFP tm2868 homozygotes. Pick WT dim GFP and check for correct segregation of progeny to maintain. tm2868 homozygotes are morphologically wild-type but show ~30% reduction in fertilized eggs and a trans-generational increase in sterility. Maintain under normal conditions. Reference: Bickel JS, et al. PLoS Genet. 2010 Jul 22;6(7):e1001028.