Entity Details

Primary name TMC6_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionQ7Z403
EntryNameTMC6_HUMAN
FullNameTransmembrane channel-like protein 6
TaxID9606
Evidenceevidence at protein level
Length805
SequenceStatuscomplete
DateCreated2005-12-06
DateModified2021-06-02

Ontological Relatives

GenesTMC6

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

Subcellular Location

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Subcellular Location
Endoplasmic reticulum membrane

Domains

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DomainNameCategoryType
IPR012496 TMC domainDomainDomain
IPR038900 Transmembrane channel-like proteinFamilyFamily

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

6 interactions