DFNA5

GSDME
Identifiers
AliasesGSDME, ICERE-1, DFNA5, DFNA5, deafness associated tumor suppressor, gasdermin E
External IDsOMIM: 608798; MGI: 1889850; HomoloGene: 3242; GeneCards: GSDME; OMA:GSDME - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_004403
NM_001127453
NM_001127454

NM_018769

RefSeq (protein)

NP_001120925
NP_001120926
NP_004394
NP_001120926.1

NP_061239

Location (UCSC)Chr 7: 24.7 – 24.76 MbChr 6: 50.17 – 50.24 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Non-syndromic hearing impairment protein 5 is a protein that in humans is encoded by the DFNA5 gene.[5][6][7]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000105928Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000029821Ensembl, 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. ^ van Camp G, Coucke P, Balemans W, van Velzen D, van de Bilt C, van Laer L, Smith RJ, Fukushima K, Padberg GW, Frants RR (Mar 1996). "Localization of a gene for non-syndromic hearing loss (DFNA5) to chromosome 7p15". Hum Mol Genet. 4 (11): 2159–63. doi:10.1093/hmg/4.11.2159. hdl:2066/20568. PMID 8589696.
  6. ^ Van Laer L, Van Camp G, van Zuijlen D, Green ED, Verstreken M, Schatteman I, Van de Heyning P, Balemans W, Coucke P, Greinwald JH, Smith RJ, Huizing E, Willems P (Mar 1998). "Refined mapping of a gene for autosomal dominant progressive sensorineural hearing loss (DFNA5) to a 2-cM region, and exclusion of a candidate gene that is expressed in the cochlea". Eur J Hum Genet. 5 (6): 397–405. doi:10.1159/000484798. PMID 9450185.
  7. ^ "Entrez Gene: DFNA5 deafness, autosomal dominant 5".