KRT6B (Keratin 6B) is a protein coding gene located on chromosome 12q13.13.
Diseases associated with KRT6B include:
- Pachyonychia congenita with mutation in KRT 17/6B (Jackson-Lawler type).
Metabolic pathways affected by this gene include developmental biology and keratinization. Functions associated with gene activity involve structural molecular activity and structural component of the cytoskeleton. An important paralog of this gene is KRT6C.