GPR179 Chromosome 17

G protein-coupled receptor 179
120 variants 120 Health Risk

Upload your DNA to see your personal genotypes for variants in GPR179.

What This Gene Does
This gene encodes a member of the glutamate receptor subfamily of G protein-coupled receptors. The encoded protein has an EGF-like calcium binding domain and a seven transmembrane domain in the N-terminal region of the protein. Mutations in this gene are associated with congenital stationary night blindness type 1E. [provided by RefSeq, Apr 2012]
Gene Info
Gene Group
G protein-coupled receptors, Class C orphans
Locus Type
gene with protein product
Location
17q12
Ensembl
ENSG00000277399
Associated Conditions (8)
Congenital stationary night blindness 1E
Inborn genetic diseases
Congenital stationary night blindness
GPR179-related disorder
Retinal dystrophy
Retinitis pigmentosa
Congenital stationary night blindness 1B
Optic atrophy
Key Variants
RS1023039979
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
Health Risk
RS112987826
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS117255299
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
Health Risk
RS1200683561
Conflicting classifications of pathogenicity
Congenital stationary night blindness, Congenital stationary night blindness
Health Risk
RS1243092519
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1329542100
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
Health Risk
RS137860025
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
Health Risk
RS144104172
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
Health Risk
RS147753316
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS147966258
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
Health Risk
RS149998444
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
Health Risk
RS181844178
Conflicting classifications of pathogenicity
Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
Health Risk
All Variants (120)
RSID Category Clinical Significance Conditions
RS1023039979 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS112987826 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS117255299 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS1200683561 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness, Congenital stationary night blindness
RS1243092519 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS1329542100 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS137860025 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS144104172 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
RS147753316 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS147966258 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS149998444 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
RS181844178 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS183799079 Health Risk Conflicting classifications of pathogenicity GPR179-related disorder, Inborn genetic diseases, GPR179-related disorder
RS185715311 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Retinal dystrophy, Congenital stationary night blindness 1E
RS187512697 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Inborn genetic diseases, Congenital stationary night blindness 1E
RS188849668 Health Risk Conflicting classifications of pathogenicity —
RS189931659 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
RS192426710 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Inborn genetic diseases, Congenital stationary night blindness 1E
RS199619898 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS199671233 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS200167781 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
RS200392643 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Inborn genetic diseases, Congenital stationary night blindness 1E
RS200421731 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS200583958 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS200731095 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS200801090 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS200936863 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Retinitis pigmentosa, Retinal dystrophy
RS201014514 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201086495 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
RS201283251 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, GPR179-related disorder, Inborn genetic diseases
RS201368251 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
RS201461684 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS201583620 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201654499 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS201772198 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS201963254 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS202030098 Health Risk Conflicting classifications of pathogenicity GPR179-related disorder, Inborn genetic diseases, GPR179-related disorder
RS202208376 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS202228440 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS281875236 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS368426715 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS369324783 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Retinal dystrophy
RS370586289 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS371603020 Health Risk Conflicting classifications of pathogenicity Retinal dystrophy, Inborn genetic diseases, Retinal dystrophy
RS372049950 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS372101002 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375898051 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, GPR179-related disorder, Congenital stationary night blindness 1E
RS375908513 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS376750375 Health Risk Conflicting classifications of pathogenicity Congenital stationary night blindness 1E, Congenital stationary night blindness 1E
RS376803348 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
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