GPR179

Protein-coding gene in the species Homo sapiens
GPR179
Identifiers
AliasesGPR179, CSNB1E, GPR158L, GPR158L1, G protein-coupled receptor 179
External IDsOMIM: 614515 MGI: 2443409 HomoloGene: 34917 GeneCards: GPR179
Gene location (Human)
Chromosome 17 (human)
Chr.Chromosome 17 (human)[1]
Chromosome 17 (human)
Genomic location for GPR179
Genomic location for GPR179
Band17q12Start38,324,571 bp[1]
End38,343,956 bp[1]
Gene location (Mouse)
Chromosome 11 (mouse)
Chr.Chromosome 11 (mouse)[2]
Chromosome 11 (mouse)
Genomic location for GPR179
Genomic location for GPR179
Band11|11 DStart97,222,935 bp[2]
End97,242,903 bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • prefrontal cortex

  • superior frontal gyrus

  • sural nerve

  • Brodmann area 9

  • skeletal muscle tissue

  • hypothalamus

  • nucleus accumbens

  • cerebellum

  • cerebellar cortex

  • cerebellar hemisphere
Top expressed in
  • hypothalamus

  • left ventricle

  • diencephalic nucleus

  • aortic valve

  • adrenal gland

  • islet of Langerhans

  • supraoptic nucleus

  • thigh

  • cerebellar cortex

  • pituitary gland
More reference expression data
BioGPS
n/a
Gene ontology
Molecular function
  • G protein-coupled receptor activity
  • signal transducer activity
Cellular component
  • integral component of membrane
  • plasma membrane
  • membrane
Biological process
  • G protein-coupled receptor signaling pathway
  • signal transduction
  • visual perception
  • response to stimulus
Sources:Amigo / QuickGO
Orthologs
SpeciesHumanMouse
Entrez

440435

217143

Ensembl

ENSG00000276469
ENSG00000277399

ENSMUSG00000070337

UniProt

Q6PRD1

E9PY61

RefSeq (mRNA)

NM_001004334

NM_001081220
NM_175453

RefSeq (protein)

NP_001004334

NP_001074689

Location (UCSC)Chr 17: 38.32 – 38.34 MbChr 11: 97.22 – 97.24 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Probable G-protein coupled receptor 179 is a protein that in humans is encoded by the GPR179 gene.[5]

Clinical relevance

Mutations in this gene have been associated to cases of congenital stationary Night Blindness.[6]

References

  1. ^ a b c ENSG00000277399 GRCh38: Ensembl release 89: ENSG00000276469, ENSG00000277399 – Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000070337 – Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ "Entrez Gene: GPR179 G protein-coupled receptor 179".
  6. ^ Audo I, Bujakowska K, Orhan E, Poloschek CM, Defoort-Dhellemmes S, Drumare I, Kohl S, Luu TD, Lecompte O, Zrenner E, Lancelot ME, Antonio A, Germain A, Michiels C, Audier C, Letexier M, Saraiva JP, Leroy BP, Munier FL, Mohand-Saïd S, Lorenz B, Friedburg C, Preising M, Kellner U, Renner AB, Moskova-Doumanova V, Berger W, Wissinger B, Hamel CP, Schorderet DF, De Baere E, Sharon D, Banin E, Jacobson SG, Bonneau D, Zanlonghi X, Le Meur G, Casteels I, Koenekoop R, Long VW, Meire F, Prescott K, de Ravel T, Simmons I, Nguyen H, Dollfus H, Poch O, Léveillard T, Nguyen-Ba-Charvet K, Sahel JA, Bhattacharya SS, Zeitz C (Feb 10, 2012). "Whole-Exome Sequencing Identifies Mutations in GPR179 Leading to Autosomal-Recessive Complete Congenital Stationary Night Blindness". American Journal of Human Genetics. 90 (2): 321–30. doi:10.1016/j.ajhg.2011.12.007. PMC 3276675. PMID 22325361.

Further reading

  • Bjarnadóttir TK, Fredriksson R, Schiöth HB (2006). "The gene repertoire and the common evolutionary history of glutamate, pheromone (V2R), taste(1) and other related G protein-coupled receptors". Gene. 362: 70–84. doi:10.1016/j.gene.2005.07.029. PMID 16229975.
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Neurotransmitter
Adrenergic
Purinergic
Serotonin
Other
Metabolites and
signaling molecules
Eicosanoid
Other
Peptide
Neuropeptide
Other
Miscellaneous
Taste, bitter
Orphan
Other
Adhesion
Orphan
Other
Taste, sweet
Other
Class F: Frizzled & Smoothened
Frizzled
Smoothened
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