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Browse result for Pachyonychia congenita

※ introduction

    Pachyonychia congenita (often abbreviated as "PC") is a rare group of autosomal dominant skin disorders that are caused by a mutation in one of five different keratin genes. Pachyonychia congenita is often associated with thickened toenails, plantar keratoderma, and plantar pain.

Reference
Wiki: Pachyonychia congenita



PTMD IDUniProt AccessionEntrez IDGene NameProtein NameOrganism
PTMD01121Q046953872
KRT17
Keratin, type I cytoskeletal 17
Homo sapiens
PTMD03665P025383853
KRT6A
Keratin, type II cytoskeletal 6A
Homo sapiens
PTMD03718P042593854
KRT6B
Keratin, type II cytoskeletal 6B
Homo sapiens
PTMD03896P087793868
KRT16
Keratin, type I cytoskeletal 16
Homo sapiens