Keratin 5, type II

Preferred Label : Keratin 5, type II;

Symbol : KRT5;

CISMeF acronym : KRT5;

Type : Gene;

Alternative titles and symbols : K5; KB5;

Ensembl ID : ENSG00000186081;

Prefixed ID : *148040;

Details

Origin ID

148040;

UMLS CUI

C1416742;

Automatic exact mappings (from CISMeF team)
- KRT5 Gene [NCIt concept]
- KRT5 wt Allele [NCIt concept]
- Keratin, Type II Cytoskeletal 5 [NCIt concept]
- keratin 5 [HGNC gene]
- keratin 5 [ORDO Gene]
HGNC gene
- keratin 5 [HGNC gene]
NCIt concept(s)
- KRT5 Gene [NCIt concept]
- KRT5 wt Allele [NCIt concept]
- Keratin, Type II Cytoskeletal 5 [NCIt concept]
ORDO concept(s)
- keratin 5 [ORDO Gene]
Phenotypes related
- Dowling-degos disease 1 [OMIM Phenotype]
- Epidermolysis bullosa simplex 2a, generalized severe [OMIM Phenotype]
- Epidermolysis bullosa simplex 2b, generalized intermediate [OMIM Phenotype]
- Epidermolysis bullosa simplex 2c, localized [OMIM Phenotype]
- Epidermolysis bullosa simplex 2d, generalized, intermediate or severe, autosomal recessive [OMIM Phenotype]
- Epidermolysis bullosa simplex 2e, with migratory circinate erythema [OMIM Phenotype]
- Epidermolysis bullosa simplex 2f, with mottled pigmentation [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KRT5 Gene [NCIt concept]
- keratin 5 [HGNC gene]

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