Variation Information: tm1598

Nametm1598 View on WormBase
Species C. elegans
Genetic positionIII:16.78 +/- 0.123 cM
Genomic positionIII: 12350856..12351370
Protein changeY75B8A.30 Deletion

Strains carrying this variation

Strain Genotype Species Description
OC271 pph-4.1(tm1598) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans Homozygous sterile mutation balanced by bli-4- and GFP-marked translocation. Heterozygotes are WT with pharyngeal GFP signal, and segregate WT GFP, arrested hT2 aneuploids, and non-GFP tm1598 homozygotes (produce ~100% dead eggs, slightly higher penetrance at 25C). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. Reference: Peters N, et al., J Cell Sci. 2010 Mar 1;123(Pt 5):795-805.