KRT1 protein, human

Preferred Label : KRT1 protein, human;

MeSH note : Mutations in the keratin K1 gene (KRT1) have been shown to underlie a variety of phenotypes typically involving generalized epidermolytic hyperkeratosis, but in some cases the phenotype can be more regionally restricted; RefSeq NM_006121;

MeSH synonym : keratin 1 (epidermolytic hyperkeratosis) protein, human; keratin 1 protein, human; Krt1-1 protein, human;

Is substance : O;

Details

Origin ID

C491616;

UMLS CUI

C1504921;

MeSH term(s) associated for indexing
- Keratin-1 [MeSH Descriptor]
Record concept(s)
- KRT1 protein, human [MeSH concept]
Semantic type(s)
- Amino Acid, Peptide, or Protein [UMLS semantic type]
- Biologically Active Substance [UMLS semantic type]
UMLS correspondences (same concept)
- Keratin, Type II Cytoskeletal 1 [NCIt concept]

Keyword's position in hierarchy(ies) :

You can consult :

recommendations
documents concerning education
documents for patients