TMC6 Products

Description

SUBCELLULAR LOCATION: Endoplasmic reticulum membrane; Multi-pass membrane protein. TISSUE SPECIFICITY: Expressed in placenta, prostate, testis, activated T-lymphocytes and lymphokine-activated killer (LAK) lymphocytes. DISEASE: Defects in TMC6 are a cause of epidermodysplasia verruciformis. It is a rare autosomal recessive genodermatosis associated with a high risk of skin carcinoma that results from an abnormal susceptibility to infection by specific human papillomaviruses. Infection leads to persistent wart-like or macular lesions.

Bioinformatics

Entrez	11322 Human
Uniprot	AAH35648 Human AAM44452 Human NP_001120670 Human NP_009198 Human Q7Z403 Human
Product By Gene ID	11322
Alternate Names	epidermodysplasia verruciformis 1 Epidermodysplasia verruciformis protein 1 EVER1FLJ17776 EVIN1EV1 expressed in activated T/LAK lymphocytes LAK-4P Protein LAK-4 transmembrane channel-like 6 transmembrane channel-like protein 6