Keratin 14, type I

Preferred Label : Keratin 14, type I;

Symbol : KRT14;

CISMeF acronym : KRT14;

Type : Gene;

Alternative titles and symbols : K14; KA14;

Ensembl ID : ENSG00000186847;

Prefixed ID : *148066;

Détails

Origin ID

148066;

UMLS CUI

C1416717;

Automatic exact mappings (from CISMeF team)
- KRT14 Gene [NCIt concept]
- KRT14 wt Allele [NCIt concept]
- Keratin, Type I Cytoskeletal 14 [NCIt concept]
- keratin 14 [HGNC gene]
- keratin 14 [ORDO Gene]
HGNC gene
- keratin 14 [HGNC gene]
NCIt concept(s)
- KRT14 Gene [NCIt concept]
- KRT14 wt Allele [NCIt concept]
- Keratin, Type I Cytoskeletal 14 [NCIt concept]
ORDO concept(s)
- keratin 14 [ORDO Gene]
Phenotypes related
- Dermatopathia pigmentosa reticularis [OMIM Phenotype]
- Epidermolysis bullosa simplex 1a, generalized severe [OMIM Phenotype]
- Epidermolysis bullosa simplex 1b, generalized intermediate [OMIM Phenotype]
- Epidermolysis bullosa simplex 1c, localized [OMIM Phenotype]
- Epidermolysis bullosa simplex 1d, generalized, intermediate or severe, autosomal recessive [OMIM Phenotype]
- Naegeli-franceschetti-jadassohn syndrome [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KRT14 Gene [NCIt concept]
- keratin 14 [HGNC gene]

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