KRT12 (Keratin 12) is a Protein Coding gene. Diseases associated with KRT12 include Meesmann Corneal Dystrophy and Corneal Dystrophy. Among its related pathways are Keratinization and Developmental Biology. KRT12 encodes the type I intermediate filament chain keratin 12, expressed in corneal epithelia. Mutations in KRT12 lead to Meesmann corneal dystrophy.