Keratin 10, type I

Preferred Label : Keratin 10, type I;

Symbol : KRT10;

CISMeF acronym : KRT10;

Type : Gene;

Alternative titles and symbols : K10; KA10;

Ensembl ID : ENSG00000186395;

Prefixed ID : *148080;

Details

Origin ID

148080;

UMLS CUI

C1416714;

Automatic exact mappings (from CISMeF team)
- KRT10 Gene [NCIt concept]
- KRT10 wt Allele [NCIt concept]
- Keratin, Type I Cytoskeletal 10 [NCIt concept]
- keratin 10 [ORDO Gene]
- keratin 10 [HGNC gene]
HGNC gene
- keratin 10 [HGNC gene]
NCIt concept(s)
- KRT10 Gene [NCIt concept]
- KRT10 wt Allele [NCIt concept]
- Keratin, Type I Cytoskeletal 10 [NCIt concept]
ORDO concept(s)
- keratin 10 [ORDO Gene]
Phenotypes related
- Epidermolytic hyperkeratosis 2a, autosomal dominant [OMIM Phenotype]
- Epidermolytic hyperkeratosis 2b, autosomal recessive [OMIM Phenotype]
- Ichthyosis hystrix, lambert type [OMIM Phenotype]
- Ichthyosis with confetti [OMIM Phenotype]
- Ichthyosis, annular epidermolytic, 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- KRT10 Gene [NCIt concept]
- keratin 10 [HGNC gene]

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