EVPL Chromosome 17

Envoplakin
1 variant 1 Health Risk

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What This Gene Does
This gene encodes a member of the plakin family of proteins that forms a component of desmosomes and the epidermal cornified envelope. This gene is located in the tylosis oesophageal cancer locus on chromosome 17q25, and its deletion is associated with both familial and sporadic forms of oesophageal squamous cell carcinoma. Patients suffering from the autoimmune mucocutaneous disorder, paraneoplastic pemphigus, develop antibodies against the encoded protein. [provided by RefSeq, Jul 2016]
Gene Info
Gene Group
"Plakins|Spectrin repeat containing"
Locus Type
gene with protein product
Location
17q25.1
Ensembl
ENSG00000167880
Key Variants
All Variants (1)
RSID Category Clinical Significance Conditions
RS367727963 Health Risk Conflicting classifications of pathogenicity
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