Variation Information: gk161

Namegk161 View on WormBase
Species C. elegans
Genetic positionIII:5.95 +/- 0.000 cM
Genomic positionIII: 11095068..11097219
Protein changeW09D6.6 Deletion

Strains carrying this variation

Strain Genotype Species Description
VC287 hmt-1(gk161) III. C. elegans W09D6.6. Superficially wild type. Attribution: This strain was provided by the C. elegans Reverse Genetics Core Facility at the University of British Columbia, which is part of the international C. elegans Gene Knockout Consortium, which should be acknowledged in any publications resulting from its use. Paper_evidence WBPaper00041807
VF14 arIs37 I; unc-119(ed3) hmt-1(gk161) III; cdIs32. C. elegans arIs37 [myo-3p::ssGFP + dpy-20(+)] I. cdIs32 [unc-122p::DT-A(E148D) + myo-2p::GFP + unc-119(+)]. Hypersensitive to cadmium. Lacks coelomocytes and accumulates GFP in pseudocoelome. Maintain under normal conditions. Reference: Schwartz MS, et al., PLoS One. 2010 Mar 5;5(3):e9564.
VF3 hmt-1(gk161) III. C. elegans Hypersensitive to cadmium; refractile inclusions in intestinal cells on Cd plates. Maintain under normal conditions. 2,149 bp deletion encompasses exons 5, 6 & 7; introduces premature stop codon. 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.