Пређи на садржај

GPR124

С Википедије, слободне енциклопедије
G protein spregnuti receptor 124
Identifikatori
Simboli GPR124; TEM5
Vanjski ID OMIM606823 MGI1925810 HomoloGene13112 IUPHAR: GPR124 GeneCards: GPR124 Gene
Pregled RNK izražavanja
podaci
Ortolozi
Vrsta Čovek Miš
Entrez 25960 78560
Ensembl ENSG00000020181 ENSMUSG00000031486
UniProt Q96PE1 Q91ZV8
RefSeq (mRNA) NM_032777.9 NM_054044.2
RefSeq (protein) NP_116166.9 NP_473385.2
Lokacija (UCSC) Chr 8:
37.64 - 37.7 Mb
Chr 8:
28.2 - 28.23 Mb
PubMed pretraga [1] [2]

G protein spregnuti receptor 124 je protein koji je kod ljudi kodiran GPR124 genom.[1][2][3]

GPR124 formira interakcije sa interact sa DLG1.[4]

  1. ^ Carson-Walter EB, Watkins DN, Nanda A, Vogelstein B, Kinzler KW, St Croix B (septembar 2001). „Cell surface tumor endothelial markers are conserved in mice and humans”. Cancer Res. 61 (18): 6649—55. PMID 11559528. 
  2. ^ Fredriksson R, Gloriam DE, Hoglund PJ, Lagerstrom MC, Schioth HB (februar 2003). „There exist at least 30 human G-protein-coupled receptors with long Ser/Thr-rich N-termini”. Biochem Biophys Res Commun. 301 (3): 725—34. PMID 12565841. doi:10.1016/S0006-291X(03)00026-3. 
  3. ^ „Entrez Gene: GPR124 G protein-coupled receptor 124”. 
  4. ^ Yamamoto, Yasunori; Irie Kenji; et al. (maj 2004). „Direct binding of the human homologue of the Drosophila disc large tumor suppressor gene to seven-pass transmembrane proteins, tumor endothelial marker 5 (TEM5), and a novel TEM5-like protein”. Oncogene. England. 23 (22): 3889—97. ISSN 0950-9232. PMID 15021905. doi:10.1038/sj.onc.1207495. 
  • Nakajima D; Okazaki N; Yamakawa H; et al. (2003). „Construction of expression-ready cDNA clones for KIAA genes: manual curation of 330 KIAA cDNA clones.”. DNA Res. 9 (3): 99—106. PMID 12168954. doi:10.1093/dnares/9.3.99. 
  • Nagase T; Kikuno R; Ishikawa K; et al. (2000). „Prediction of the coding sequences of unidentified human genes. XVII. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.”. DNA Res. 7 (2): 143—50. PMID 10819331. doi:10.1093/dnares/7.2.143. 
  • 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. PMC 139241Слободан приступ. PMID 12477932. doi:10.1073/pnas.242603899. 
  • 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. PMID 14702039. doi:10.1038/ng1285. 
  • Yamamoto Y; Irie K; Asada M; et al. (2004). „Direct binding of the human homologue of the Drosophila disc large tumor suppressor gene to seven-pass transmembrane proteins, tumor endothelial marker 5 (TEM5), and a novel TEM5-like protein.”. Oncogene. 23 (22): 3889—97. PMID 15021905. doi:10.1038/sj.onc.1207495. 
  • Bjarnadóttir TK; Fredriksson R; Höglund PJ; et al. (2005). „The human and mouse repertoire of the adhesion family of G-protein-coupled receptors.”. Genomics. 84 (1): 23—33. PMID 15203201. doi:10.1016/j.ygeno.2003.12.004. 
  • Vallon M, Essler M (2006). „Proteolytically processed soluble tumor endothelial marker (TEM) 5 mediates endothelial cell survival during angiogenesis by linking integrin alpha(v)beta3 to glycosaminoglycans.”. J. Biol. Chem. 281 (45): 34179—88. PMID 16982628. doi:10.1074/jbc.M605291200.