Variation Information: n5453

Namen5453 View on WormBase
Species C. elegans
Genetic positionI:3.52 +/- 0.000 cM
Genomic positionI: 9078307..9079234
Protein changeT06D10.2 Deletion

Strains carrying this variation

Strain Genotype Species Description
MT20434 chaf-1(n5453) I/hT2 [bli-4(e937) let-?(q782) qIs48] (I;III). C. elegans Heterozygotes are WT and GFP+ in the pharynx. qIs48 is an insertion of ccEx9747 (carries myo-2::GFP, pes-10::GFP, and a gut enhancer fused to GFP) onto the hT2 chromosome and is homozygous lethal. Presence of ces-1 is inferred from strain construction but not experimentally verified. Note: qIs48 has been observed to recombine off hT2, typically leaving behind a functional homozygous viable hT2 with Bli-4 phenotype. Reference: Nakano S, et al. Cell. 2011 Dec 23;147(7):1525-36.