TMC8

TMC8
Identifiers
AliasesTMC8, EV2, EVER2, EVIN2, transmembrane channel like 8
External IDsMGI: 2669037 HomoloGene: 45126 GeneCards: TMC8
Gene location (Human)
Chr.Chromosome 17 (human)[1]
BandNo data availableStart78,130,770 bp[1]
End78,142,968 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

147138

217356

Ensembl

ENSG00000167895

ENSMUSG00000050106

UniProt

Q8IU68

Q7TN58

RefSeq (mRNA)

NM_152468

NM_001195088
NM_001195089
NM_001195090
NM_181856

RefSeq (protein)

NP_689681

NP_001182017
NP_001182018
NP_001182019
NP_862904

Location (UCSC)Chr 17: 78.13 – 78.14 MbChr 17: 117.78 – 117.79 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Transmembrane channel-like 8 is a protein which in humans is encoded by the TMC8 gene.[5][6]

Function

The protein encoded by this gene is an integral membrane protein that localize to the endoplasmic reticulum and is predicted to form transmembrane channels. This gene encodes a transmembrane channel-like protein with 8 predicted transmembrane domains and 3 leucine zipper motifs.[6]

Clinical significance

Mutations in the TMC8 gene are associated with epidermodysplasia verruciformis (EV), an autosomal recessive dermatosis characterized by abnormal susceptibility to human papillomaviruses (HPVs) and a high rate of progression to squamous cell carcinoma on sun-exposed skin.[6]

References

  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000167895 - Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000050106 - Ensembl, May 2017
  3. "Human PubMed Reference:".
  4. "Mouse PubMed Reference:".
  5. Ramoz N, Rueda LA, Bouadjar B, Montoya LS, Orth G, Favre M (December 2002). "Mutations in two adjacent novel genes are associated with epidermodysplasia verruciformis". Nature Genetics. 32 (4): 579–81. PMID 12426567. doi:10.1038/ng1044.
  6. 1 2 3 "Entrez Gene: TMC8 transmembrane channel-like 8".

Further reading

This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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