GPR179
protein-coding gene in the species Homo sapiens
Facts
13 properties- Instance of
- gene
- Subclass of
- protein-coding gene
- Chromosome
- human chromosome 17[13]
- Cytogenetic location
- 17q12[16]
- Encodes
- G protein-coupled receptor 179, Probable G-protein-coupled receptor 179[10][11]
- Expressed in
- testicle, prefrontal cortex, superior frontal gyrus, sural nerve, primary visual cortex, Brodmann area 9, skeletal muscle tissue, hypothalamus, right frontal lobe, nucleus accumbens[17][18][19][20][21][22][23][24][25][26]
- Found in taxon
- Homo sapiens[12]
- Genetic association
- congenital stationary night blindness 1E[14]
- HomoloGene ID
- 34917[3]
- Strand orientation
- reverse strand[15]
🏷️ Also known as
en CSNB1E
en GPR158L
en GPR158L1
en GPR179
en G protein-coupled receptor 179
🔖 Identifiers · 10
- Ensembl gene ID
- ENSG00000276469, ENSG00000277399
- Ensembl transcript ID
- ENST00000610867, ENST00000616987, ENST00000622573, ENST00000610650
- Entrez Gene ID
- 440435
- Exact match
- identifiers.org
- Freebase ID
- /m/03d41dc
- HGNC ID
- 31371
- HGNC gene symbol
- GPR179
- OMIM ID
- 614515
- RefSeq RNA ID
- NM_001004334
- UMLS CUI
- C1825411
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