GPR119
From Wikipedia, the free encyclopedia
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G protein-coupled receptor 119
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| Identifiers | ||||||||||||||
| Symbol(s) | GPR119; GPCR2; MGC119957; hGPCR2 | |||||||||||||
| External IDs | OMIM: 300513 MGI: 2668412 HomoloGene: 18670 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 139760 | 236781 | ||||||||||||
| Ensembl | ENSG00000147262 | ENSMUSG00000051209 | ||||||||||||
| Uniprot | Q8TDV5 | Q2ABS2 | ||||||||||||
| Refseq | NM_178471 (mRNA) NP_848566 (protein) |
NM_181751 (mRNA) NP_861416 (protein) |
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| Location | Chr X: 129.35 - 129.35 Mb | Chr X: 44.92 - 44.92 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
G protein-coupled receptor 119, also known as GPR119, is a human gene.[1]
GPR119 is a member of the rhodopsin family of G protein-coupled receptors (GPRs) (Fredriksson et al., 2003).[supplied by OMIM][1]
[edit] References
[edit] Further reading
- Takeda S, Kadowaki S, Haga T, et al. (2002). "Identification of G protein-coupled receptor genes from the human genome sequence.". FEBS Lett. 520 (1-3): 97–101. PMID 12044878.
- Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences.". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:. PMID 12477932.
- Fredriksson R, Höglund PJ, Gloriam DE, et al. (2003). "Seven evolutionarily conserved human rhodopsin G protein-coupled receptors lacking close relatives.". FEBS Lett. 554 (3): 381–8. PMID 14623098.
- Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:. PMID 15489334.
- Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature 434 (7031): 325–37. doi:. PMID 15772651.
- Overton HA, Babbs AJ, Doel SM, et al. (2006). "Deorphanization of a G protein-coupled receptor for oleoylethanolamide and its use in the discovery of small-molecule hypophagic agents.". Cell Metab. 3 (3): 167–75. doi:. PMID 16517404.

