KRT76
Description
The KRT76 (keratin 76) is a protein-coding gene located on chromosome 12.
KRT76 is a gene that encodes a keratin protein. Reduced expression or activity of this gene has been linked to the development of oral cancer.
KRT76 likely contributes to the process of terminal cornification.
KRT76 is also known as HUMCYT2A, KRT2B, KRT2P.
Associated Diseases
- low grade glioma
- hypotrichosis simplex
- uncombable hair syndrome
- Dowling-Degos disease
- hereditary palmoplantar keratoderma, Gamborg-Nielsen type
- hyperpigmentation with or without hypopigmentation, familial progressive
- erythrokeratodermia variabilis
- focal palmoplantar and gingival keratoderma
- ringed hair disease
- disseminated superficial actinic porokeratosis
- pili bifurcati
- wooly hair, autosomal recessive 3
- epidermolytic palmoplantar keratoderma
- hypotrichosis 4
- keratosis linearis-ichthyosis congenita-sclerosing keratoderma syndrome
- ichthyosis, lamellar, autosomal dominant
- pili torti