※ PTMD 2.0 database Online Browse Options
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
Reference
Wiki: Pachyonychia congenita
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01121 | Q04695 | 3872 | KRT17 | Keratin, type I cytoskeletal 17 | Homo sapiens |
| PTMD03665 | P02538 | 3853 | KRT6A | Keratin, type II cytoskeletal 6A | Homo sapiens |
| PTMD03718 | P04259 | 3854 | KRT6B | Keratin, type II cytoskeletal 6B | Homo sapiens |
| PTMD03896 | P08779 | 3868 | KRT16 | Keratin, type I cytoskeletal 16 | Homo sapiens |
