Variation Information: tm514

Nametm514 View on WormBase
Species C. elegans
Genetic positionIII:-1.45 +/- 0.000 cM
Genomic positionIII: 5724307..5724729
Protein changeB0336.1a B0336.1b Deletion

Strains carrying this variation

Strain Genotype Species Description
HS732 wrm-1(tm514) III/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans Homozygous lethal deletion chromosome 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 tm514 homozygotes (probable embryonic or early larval arrest). Homozygous hT2[bli-4 let-? qIs48] inviable. Note: qIs48 has been observed to recombine off hT2, typically leaving behind a functional homozygous viable hT2 with Bli-4 phenotype. Pick WT GFP and check for correct segregation of progeny to maintain.
WM75 wrm-1(tm514) III; neIs2 IV. C. elegans neIs2 [wrm-1::GFP + rol-6(su1006)] IV. Rollers.