GPRC5C
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| G protein spregnuti receptor, familija C, grupa 5, član C | |||||||||||
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| Identifikatori | |||||||||||
| Simboli | GPRC5C; RAIG-3; RAIG3 | ||||||||||
| Vanjski ID | OMIM: 605949 MGI: 1917605 HomoloGene: 11099 IUPHAR: RAIG3 GeneCards: GPRC5C Gene | ||||||||||
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| Pregled RNK izražavanja | |||||||||||
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| podaci | |||||||||||
| Ortolozi | |||||||||||
| Vrsta | Čovek | Miš | |||||||||
| Entrez | 55890 | 70355 | |||||||||
| Ensembl | ENSG00000170412 | ENSMUSG00000051043 | |||||||||
| UniProt | Q9NQ84 | Q8K3J9 | |||||||||
| RefSeq (mRNA) | NM_018653.3 | NM_001110337.1 | |||||||||
| RefSeq (protein) | NP_061123.3 | NP_001103807.1 | |||||||||
| Lokacija (UCSC) | Chr 17: 72.43 - 72.45 Mb | Chr 11: 114.71 - 114.73 Mb | |||||||||
| PubMed pretraga | [1] | [2] | |||||||||
G protein spregnuti receptor, familija C, grupa 5, član C je protein koji je kod ljudi kodiran GPRC5C genom.[1][2]
Ovaj protein pripada familiji tipa 3 G protein spregnutih receptora, koja ima karakteristični 7-transmembranski domen. On potencijalno učestvuje u interakciji između retinoidne kiseline i G protein signalnih puteva. Retinoinska kiselina ima kritičnu ulogu u razvoju, ćelijskom rastu, i diferencijaciji. Ovaj gen potencijalno učestvuje u embrionskom razvoju i diferencijaciji epitelnih ćelija.[2]
- ↑ Robbins MJ, Michalovich D, Hill J, Calver AR, Medhurst AD, Gloger I, Sims M, Middlemiss DN, Pangalos MN (Nov 2000). „Molecular cloning and characterization of two novel retinoic acid-inducible orphan G-protein-coupled receptors (GPRC5B and GPRC5C)”. Genomics 67 (1): 8–18. DOI:10.1006/geno.2000.6226. PMID 10945465.
- ↑ 2,0 2,1 „Entrez Gene: GPRC5C G protein-coupled receptor, family C, group 5, member C”.
- Maruyama K, Sugano S (1994). „Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides”. Gene 138 (1–2): 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID 8125298.
- Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, (1997). „Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library”. Gene 200 (1–2): 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID 9373149.
- Bräuner-Osborne H, Krogsgaard-Larsen P (2000). „Sequence and expression pattern of a novel human orphan G-protein-coupled receptor, GPRC5B, a family C receptor with a short amino-terminal domain”. Genomics 65 (2): 121–8. DOI:10.1006/geno.2000.6164. PMID 10783259.
- Bräuner-Osborne H, Jensen AA, Sheppard PO, (2001). „Cloning and characterization of a human orphan family C G-protein coupled receptor GPRC5D”. Biochim. Biophys. Acta 1518 (3): 237–48. PMID 11311935.
- Strausberg RL, Feingold EA, Grouse LH, (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.
- Lehner B, Semple JI, Brown SE, (2004). „Analysis of a high-throughput yeast two-hybrid system and its use to predict the function of intracellular proteins encoded within the human MHC class III region”. Genomics 83 (1): 153–67. DOI:10.1016/S0888-7543(03)00235-0. PMID 14667819.
- Ota T, Suzuki Y, Nishikawa T, (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, (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.
- Rual JF, Venkatesan K, Hao T, (2005). „Towards a proteome-scale map of the human protein-protein interaction network”. Nature 437 (7062): 1173–8. DOI:10.1038/nature04209. PMID 16189514.
- Otsuki T, Ota T, Nishikawa T, (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.
- „GPRC5 Receptors: RAIG3”. IUPHAR Database of Receptors and Ion Channels. International Union of Basic and Clinical Pharmacology. Arhivirano iz originala na datum 2016-03-04.