GPR34
From Wikipedia, the free encyclopedia
| G protein-coupled receptor 34 | ||||||||
|---|---|---|---|---|---|---|---|---|
| Identifiers | ||||||||
| Symbol | GPR34 | |||||||
| External IDs | OMIM: 300241 MGI: 1346334 HomoloGene: 36174 IUPHAR: GPR34 GeneCards: GPR34 Gene | |||||||
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| Orthologs | ||||||||
| Species | Human | Mouse | ||||||
| Entrez | 2857 | 23890 | ||||||
| Ensembl | ENSG00000171659 | ENSMUSG00000040229 | ||||||
| UniProt | Q9UPC5 | Q9R1K6 | ||||||
| RefSeq (mRNA) | NM_001033513.2 | NM_011823.4 | ||||||
| RefSeq (protein) | NP_001091048.1 | NP_035953.3 | ||||||
| Location (UCSC) | Chr X: 41.55 – 41.56 Mb |
Chr X: 13.63 – 13.64 Mb |
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| PubMed search | [1] | [2] | ||||||
Probable G-protein coupled receptor 34 is a protein that in humans is encoded by the GPR34 gene.[1][2][3]
G protein-coupled receptors (GPCRs), such as GPR34, are integral membrane proteins containing 7 putative transmembrane domains (TMs). These proteins mediate signals to the interior of the cell via activation of heterotrimeric G proteins that in turn activate various effector proteins, ultimately resulting in a physiologic response.[supplied by OMIM][3]
[edit] References
- ^ Schoneberg T, Schulz A, Grosse R, Schade R, Henklein P, Schultz G, Gudermann T (Aug 1999). "A novel subgroup of class I G-protein-coupled receptors". Biochim Biophys Acta 1446 (1–2): 57–70. PMID 10395919.
- ^ Marchese A, Sawzdargo M, Nguyen T, Cheng R, Heng HH, Nowak T, Im DS, Lynch KR, George SR, O'dowd BF (May 1999). "Discovery of three novel orphan G-protein-coupled receptors". Genomics 56 (1): 12–21. doi:10.1006/geno.1998.5655. PMID 10036181.
- ^ a b "Entrez Gene: GPR34 G protein-coupled receptor 34". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2857.
[edit] Further reading
- Hillier LD, Lennon G, Becker M, et al. (1997). "Generation and analysis of 280,000 human expressed sequence tags". Genome Res. 6 (9): 807–28. doi:10.1101/gr.6.9.807. PMID 8889549.
- Jacobi FK, Broghammer M, Pesch K, et al. (2000). "Physical mapping and exclusion of GPR34 as the causative gene for congenital stationary night blindness type 1". Hum. Genet. 107 (1): 89–91. doi:10.1007/s004390050017. PMID 10982042.
- 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:10.1073/pnas.242603899. PMC 139241. PMID 12477932. //www.ncbi.nlm.nih.gov/pmc/articles/PMC139241/.
- Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
- 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:10.1101/gr.2596504. PMC 528928. PMID 15489334. //www.ncbi.nlm.nih.gov/pmc/articles/PMC528928/.
- Otsuki T, Ota T, Nishikawa T, et al. (2007). "Signal sequence and keyword trap in silico for selection of full-length human cDNAs encoding secretion or membrane proteins from oligo-capped cDNA libraries". DNA Res. 12 (2): 117–26. doi:10.1093/dnares/12.2.117. PMID 16303743.
- Engemaier E, Römpler H, Schöneberg T, Schulz A (2006). "Genomic and supragenomic structure of the nucleotide-like G-protein-coupled receptor GPR34". Genomics 87 (2): 254–64. doi:10.1016/j.ygeno.2005.10.001. PMID 16338117.
- Oh JH, Yang JO, Hahn Y, et al. (2006). "Transcriptome analysis of human gastric cancer". Mamm. Genome 16 (12): 942–54. doi:10.1007/s00335-005-0075-2. PMID 16341674.
- Liebscher I, Müller U, Teupser D, et al. (2011). "Altered immune response in mice deficient for the G protein-coupled receptor GPR34". J Biol Chem. 286 (3): 2101-10. doi:10.1074/jbc.M110.196659. PMC 3023507. PMID 21097509. //www.ncbi.nlm.nih.gov/pmc/articles/PMC3023507/.
- Ritscher L, Engemaier E, Stäubert C, et al. (2012). "The ligand specificity of the G-protein-coupled receptor GPR34". Biochem J. 443 (3): 841-50. doi:10.1042/BJ20112090. PMID 22348703.
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