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Browse result for Steatocystoma multiplex
※ introduction A sebaceous gland disease characterized by the presence of multiple benign sebaceous cysts that has_material_basis_in heterozygous mutation in the KRT17 gene on chromosome 17q21.2.
Reference
DiseaseOntology: Steatocystoma multiplex
Reference
DiseaseOntology: Steatocystoma multiplex
| PTMD ID | UniProt Accession | Entrez ID | Gene Name | Protein Name | Organism |
|---|---|---|---|---|---|
| PTMD01121 | Q04695 | 3872 | KRT17 | Keratin, type I cytoskeletal 17 | Homo sapiens |