GPR35
From Wikipedia, the free encyclopedia
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G protein-coupled receptor 35
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| Identifiers | ||||||||||||||
| Symbol(s) | GPR35; | |||||||||||||
| External IDs | OMIM: 602646 MGI: 1929509 HomoloGene: 3874 | |||||||||||||
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| RNA expression pattern | ||||||||||||||
| Orthologs | ||||||||||||||
| Human | Mouse | |||||||||||||
| Entrez | 2859 | 64095 | ||||||||||||
| Ensembl | ENSG00000178623 | ENSMUSG00000026271 | ||||||||||||
| Uniprot | Q9HC97 | Q3TBY9 | ||||||||||||
| Refseq | NM_005301 (mRNA) NP_005292 (protein) |
NM_022320 (mRNA) NP_071715 (protein) |
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| Location | Chr 2: 241.22 - 241.22 Mb | Chr 1: 94.62 - 94.82 Mb | ||||||||||||
| Pubmed search | [1] | [2] | ||||||||||||
GPR35 is a G protein-coupled receptor discovered in 1998.[1] Hightened expression of GPR35 is found in immune and gastrointestinal tissues, including the crypts of Lieberkühn.
[edit] Ligands
One study has shown that kynurenic acid acts as an endogenous ligand for this receptor.[2] Zaprinast, a PDE5A inhibitor, was found to be an agonist for GPR35.[3]
[edit] Role in pathology
Deletion of GPR35 gene may be responsible for brachydactyly mental retardation syndrome.[4]In one study GPR35 has been recognised as a potential oncogene in the stomach cancer.[5]
[edit] References
- ^ O'Dowd BF, Nguyen T, Marchese A, Cheng R, Lynch KR, Heng HH, Kolakowski LF, George SR (1998). "Discovery of three novel G-protein-coupled receptor genes". Genomics 47 (2): 310–3. doi:. PMID 9479505.
- ^ Wang J, Simonavicius N, Wu X, Swaminath G, Reagan J, Tian H, Ling L (2006). "Kynurenic acid as a ligand for orphan G protein-coupled receptor GPR35". J. Biol. Chem. 281 (31): 22021–8. doi:. PMID 16754668.free fulltext
- ^ Taniguchi Y, Tonai-Kachi H, Shinjo K (2006). "Zaprinast, a well-known cyclic guanosine monophosphate-specific phosphodiesterase inhibitor, is an agonist for GPR35". FEBS Lett. 580 (21): 5003–8. doi:. PMID 16934253.
- ^ Shrimpton AE, Braddock BR, Thomson LL, Stein CK, Hoo JJ (2004). "Molecular delineation of deletions on 2q37.3 in three cases with an Albright hereditary osteodystrophy-like phenotype". Clin. Genet. 66 (6): 537–44. doi:. PMID 15521982.
- ^ Okumura S, Baba H, Kumada T, Nanmoku K, Nakajima H, Nakane Y, Hioki K, Ikenaka K (2004). "Cloning of a G-protein-coupled receptor that shows an activity to transform NIH3T3 cells and is expressed in gastric cancer cells". Cancer Sci. 95 (2): 131–5. PMID 14965362.

