Variation Information: tn1540

Nametn1540 View on WormBase
Species C. elegans
Genetic positionI:-3.12 +/- 0.000 cM
Genomic positionI: 3612348..3618056
Protein changeY47G6A.1 Deletion

Strains carrying this variation

Strain Genotype Species Description
DG3887 inx-21(tn1540) I/hT2[bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans Homozygous sterile allele 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 sterile homozygotes (inx-21(tn1540) homozygous animals are sterile, producing few germ cells). Homozygous hT2[bli-4 let-? qIs48] inviable. Pick WT GFP and check for correct segregation of progeny to maintain. Reference: Starich TA, Hall DH, Greenstein D. Genetics. 2014 Nov;198(3):1127-53.