Entity Details

Primary name TMC6
Entity type gene
Source Source Link

Details

PrimaryID11322
RefseqGeneNG_007879
SymbolTMC6
Nametransmembrane channel like 6
Chromosome17
Location17q25.3
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate1999-09-17
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsTMC6_HUMAN

GO terms

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GOName
GO:0005737 cytoplasm
GO:0005783 endoplasmic reticulum
GO:0005789 endoplasmic reticulum membrane
GO:0005794 Golgi apparatus
GO:0005886 plasma membrane
GO:0005887 integral component of plasma membrane
GO:0008381 mechanosensitive ion channel activity
GO:0031965 nuclear membrane
GO:0035579 specific granule membrane
GO:0043312 neutrophil degranulation
GO:0070062 extracellular exosome
GO:0070821 tertiary granule membrane

Diseases

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Disease IDSourceNameDescription
226400 OMIMEpidermodysplasia verruciformis 1 (EV1)A form of epidermodysplasia verruciformis, a rare genodermatosis associated with a high risk of skin carcinoma that results from an abnormal susceptibility to infection by specific human papillomaviruses, including the oncogenic HPV5. Infection leads to the early development of disseminated flat wart-like and pityriasis versicolor-like skin lesions. Cutaneous Bowen's carcinomas in situ and invasive squamous cell carcinomas develop in about half of the patients, mainly on sun-exposed skin areas. EV1 inheritance is autosomal recessive. The disease is caused by variants affecting the gene represented in this entry.

Interactions

14 interactions