3TNU386116664ENSG00000186847ENSMUSG00000045545P02533Q61781NM_000526NM_016958NM_001313956NM_001313957NP_000517NP_001300885NP_001300886NP_058654Keratin 14 is a member of the type I keratin family of intermediate filament proteins.

In humans it is encoded by the KRT14 gene.

[6][7][8] Keratin 14 is usually found as a heterodimer with type II keratin 5 and form the cytoskeleton of epithelial cells.

Mutations in the genes for these keratins are associated with epidermolysis bullosa simplex[9] and dermatopathia pigmentosa reticularis, both of which are autosomal dominant mutations.

This article on a gene on human chromosome 17 is a stub.