Variation Information: tm1748

Nametm1748 View on WormBase
Species C. elegans
Genetic positionII:3.77 +/- 0.005 cM
Genomic positionII: 11576985..11577572
Protein changeF54D5.1a F54D5.1b Deletion

Strains carrying this variation

Strain Genotype Species Description
VF2 pcs-1(tm1748) II. C. elegans Hypersensitive to cadmium. Maintain under normal conditions. 588 bp deletion + 3 bp insertion [36918/36919 - AAA - 37506/37507]. Reference: Schwartz MS, et al., PLoS One. 2010 Mar 5;5(3):e9564.
VF9 pcs-1(tm1748) II; hmt-1(gk161) III. C. elegans Acute hypersensitivity to heavy metals (Cd, As, Cu). Reference: Schwartz MS, et al., PLoS One. 2010 Mar 5;5(3):e9564.