EMP2

EMP2
Identifiers
AliasesEMP2, NPHS10, XMP, epithelial membrane protein 2
External IDsOMIM: 602334; MGI: 1098726; HomoloGene: 1089; GeneCards: EMP2; OMA:EMP2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

2013

13731

Ensembl

ENSG00000213853

ENSMUSG00000022505

UniProt

P54851

O88662

RefSeq (mRNA)

NM_001424

NM_007929

RefSeq (protein)

NP_001415

NP_031955

Location (UCSC)Chr 16: 10.53 – 10.58 MbChr 16: 10.1 – 10.13 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Epithelial membrane protein 2 is a protein that in humans is encoded by the EMP2 gene.[5][6][7][8]

Clinical significance

Mutations in EMP2 cause childhood-onset nephrotic syndrome.[9]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000213853 Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000022505 Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. Ben-Porath I, Benvenisty N (Feb 1997). "Characterization of a tumor-associated gene, a member of a novel family of genes encoding membrane glycoproteins". Gene. 183 (1–2): 69–75. doi:10.1016/S0378-1119(96)00475-1. PMID 8996089.
  6. Liehr T, Kuhlenbaumer G, Wulf P, Taylor V, Suter U, Van Broeckhoven C, et al. (Jul 1999). "Regional localization of the human epithelial membrane protein genes 1, 2, and 3 (EMP1, EMP2, EMP3) to 12p12.3, 16p13.2, and 19q13.3". Genomics. 58 (1): 106–8. doi:10.1006/geno.1999.5803. PMID 10331954.
  7. Wadehra M, Forbes A, Pushkarna N, Goodglick L, Gordon LK, Williams CJ, et al. (Nov 2005). "Epithelial membrane protein-2 regulates surface expression of alphavbeta3 integrin in the endometrium". Dev Biol. 287 (2): 336–45. doi:10.1016/j.ydbio.2005.09.003. PMID 16216233.
  8. "Entrez Gene: EMP2 epithelial membrane protein 2".
  9. Gee HY, Ashraf S, Wan X, Vega-Warner V, Esteve-Rudd J, Lovric S, et al. (June 2014). "Mutations in EMP2 cause childhood-onset nephrotic syndrome". American Journal of Human Genetics. 94 (6): 884–890. doi:10.1016/j.ajhg.2014.04.010. PMC 4121470. PMID 24814193.

Further reading


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