KRT14 (Keratin 14) is a Protein Coding gene. Diseases associated with KRT14 include Epidermolysis Bullosa Simplex, Koebner Type and Epidermolysis Bullosa Simplex, Recessive 1. Among its related pathways are Corticotropin-releasing hormone signaling pathway and Glucocorticoid receptor regulatory network. GO annotations related to this gene include structural molecule activity and keratin filament binding. An important paralog of this gene is KRT16. KRT17 (Keratin 17) is a Protein Coding gene. Diseases associated with KRT17 include Steatocystoma Multiplex and Pachyonychia Congenita 2. Among its related pathways are Glucocorticoid receptor regulatory network and Keratinization. GO annotations related to this gene include structural molecule activity and MHC class II receptor activity. An important paralog of this gene is KRT14.