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GPR12

From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
GPR12
Identifiers
AliasesGPR12, GPCR12, GPCR21, PPP1R84, G protein-coupled receptor 12
External IDsOMIM:600752;MGI:101909;HomoloGene:3868;GeneCards:GPR12;OMA:GPR12 - orthologs
Gene location (Human)
Chromosome 13 (human)
Chr.Chromosome 13 (human)[1]
Chromosome 13 (human)
Genomic location for GPR12
Genomic location for GPR12
Band13q12.13Start26,755,200bp[1]
End26,760,786bp[1]
Gene location (Mouse)
Chromosome 5 (mouse)
Chr.Chromosome 5 (mouse)[2]
Chromosome 5 (mouse)
Genomic location for GPR12
Genomic location for GPR12
Band5|5 G3Start146,519,208bp[2]
End146,522,049bp[2]
RNA expression pattern
Bgee
HumanMouse (ortholog)
Top expressed in
  • ganglionic eminence

  • cerebellar hemisphere

  • right hemisphere of cerebellum

  • nucleus accumbens

  • caudate nucleus

  • prefrontal cortex

  • putamen

  • Brodmann area 9

  • cingulate gyrus

  • anterior cingulate cortex
Top expressed in
  • perirhinal cortex

  • entorhinal cortex

  • CA3 field

  • primary visual cortex

  • superior frontal gyrus

  • dentate gyrus of hippocampal formation granule cell

  • hippocampus proper

  • Region I of hippocampus proper

  • dorsal striatum

  • nucleus of stria terminalis
More reference expression data
BioGPS
More reference expression data
Gene ontology
Molecular function
Cellular component
Biological process
Sources:Amigo /QuickGO
Orthologs
SpeciesHumanMouse
Entrez

2835

14738

Ensembl

ENSG00000132975

ENSMUSG00000041468

UniProt

P47775

P35412

RefSeq (mRNA)

NM_005288

NM_001010941
NM_008151
NM_001359055
NM_001359056
NM_001359057

NM_001359058

RefSeq (protein)

NP_005279

NP_001010941
NP_032177
NP_001345984
NP_001345985
NP_001345986

NP_001345987

Location (UCSC)Chr 13: 26.76 – 26.76 MbChr 5: 146.52 – 146.52 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Probable G-protein coupled receptor 12 is aprotein that in humans is encoded by theGPR12gene.[5][6][7]

The gene product of GPR12 is anorphan receptor, meaning that its endogenousligand is currently unknown. Gene disruption of GPR12 in mice results indyslipidemia and obesity.[8]

Ligands

[edit]
Inverse agonists

Evolution

[edit]

Paralogues

[edit]

Source:[10]

References

[edit]
  1. ^abcGRCh38: Ensembl release 89: ENSG00000132975Ensembl, May 2017
  2. ^abcGRCm38: Ensembl release 89: ENSMUSG00000041468Ensembl, 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. ^Saeki Y, Ueno S, Mizuno R, Nishimura T, Fujimura H, Nagai Y, Yanagihara T (December 1993)."Molecular cloning of a novel putative G protein-coupled receptor (GPCR21) which is expressed predominantly in mouse central nervous system".FEBS Letters.336 (2):317–22.doi:10.1016/0014-5793(93)80828-I.PMID 8262253.S2CID 31345248.
  6. ^Song ZH, Modi W, Bonner TI (July 1995)."Molecular cloning and chromosomal localization of human genes encoding three closely related G protein-coupled receptors".Genomics.28 (2):347–9.doi:10.1006/geno.1995.1154.PMID 8530049.
  7. ^"Entrez Gene: GPR12 G protein-coupled receptor 12".
  8. ^Bjursell M, Gerdin AK, Jönsson M, Surve VV, Svensson L, Huang XF, et al. (September 2006). "G protein-coupled receptor 12 deficiency results in dyslipidemia and obesity in mice".Biochemical and Biophysical Research Communications.348 (2):359–66.doi:10.1016/j.bbrc.2006.07.090.PMID 16887097.
  9. ^Brown KJ, Laun AS, Song ZH (November 2017)."Cannabidiol, a novel inverse agonist for GPR12".Biochemical and Biophysical Research Communications.493 (1):451–454.doi:10.1016/j.bbrc.2017.09.001.PMC 5849771.PMID 28888984.
  10. ^"GeneCards®: The Human Gene Database".

Further reading

[edit]
  • Uhlenbrock K, Huber J, Ardati A, Busch AE, Kostenis E (2003). "Fluid shear stress differentially regulates gpr3, gpr6, and gpr12 expression in human umbilical vein endothelial cells".Cellular Physiology and Biochemistry.13 (2):75–84.doi:10.1159/000070251.PMID 12649592.S2CID 45156405.
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