TMEM47

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Transmembrane protein 47
Identifiers
Symbol(s) TMEM47; BCMP1; DKFZP761J17121; DKFZp564E153; MGC32949; TM4SF10
External IDs MGI: 2177570 HomoloGene: 41830
RNA expression pattern

More reference expression data
Orthologs
Human Mouse
Entrez 83604 192216
Ensembl ENSG00000147027 ENSMUSG00000025666
Uniprot Q9BQJ4 Q9JJG6
Refseq NM_031442 (mRNA)
NP_113630 (protein)		 NM_138751 (mRNA)
NP_620090 (protein)
Location Chr X: 34.56 - 34.59 Mb Chr X: 77.32 - 77.35 Mb
Pubmed search [1] [2]

Transmembrane protein 47, also known as TMEM47, is a human gene.[1]

This gene encodes a member of the PMP22/EMP/claudin protein family. The encoded protein is localized to the ER and the plasma membrane. In dogs, transcripts of this gene exist at high levels in the brain.[1]

[edit] References

  1. ^ a b Entrez Gene: TMEM47 transmembrane protein 47.

[edit] Further reading

  • Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination.". Genome Res. 10 (11): 1788–95. PMID 11076863. 
  • Wiemann S, Weil B, Wellenreuther R, et al. (2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs.". Genome Res. 11 (3): 422–35. doi:10.1101/gr.154701. PMID 11230166. 
  • Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing.". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMID 11256614. 
  • Christophe-Hobertus C, Szpirer C, Guyon R, Christophe D (2003). "Identification of the gene encoding Brain Cell Membrane Protein 1 (BCMP1), a putative four-transmembrane protein distantly related to the Peripheral Myelin Protein 22 / Epithelial Membrane Proteins and the Claudins.". BMC Genomics 2 (1): 3. PMID 11472633. 
  • 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. PMID 12477932. 
  • 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. 
  • Christophe-Hobertus C, Kooy F, Gecz J, et al. (2004). "TM4SF10 gene sequencing in XLMR patients identifies common polymorphisms but no disease-associated mutation.". BMC Med. Genet. 5: 22. doi:10.1186/1471-2350-5-22. PMID 15345028. 
  • 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. PMID 15489334. 
  • Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline.". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMID 15489336. 
  • Ross MT, Grafham DV, Coffey AJ, et al. (2005). "The DNA sequence of the human X chromosome.". Nature 434 (7031): 325–37. doi:10.1038/nature03440. PMID 15772651. 
  • Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006.". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMID 16381901. 
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