Cytochrome p450, subfamily xxvib, polypeptide 1

Preferred Label : Cytochrome p450, subfamily xxvib, polypeptide 1;

Symbol : CYP26B1;

CISMeF acronym : CYP26B1;

Type : Gene;

Alternative titles and symbols : Cytochrome p450, subfamily xxvia, polypeptide 2; P450, retinoic acid-inactivating, 2; CYP26A2; P450RAI2;

Ensembl ID : ENSG00000003137;

Prefixed ID : *605207;

Details

Origin ID

605207;

UMLS CUI

C1427015;

Automatic exact mappings (from CISMeF team)
- CYP26B1 Gene [NCIt concept]
- CYP26B1 wt Allele [NCIt concept]
- Cytochrome P450 26B1 [NCIt concept]
- Retinoic Acid 4-Hydroxylase [MeSH Descriptor]
- cytochrome P450 family 26 subfamily B member 1 [ORDO Gene]
- cytochrome P450 family 26 subfamily B member 1 [HGNC gene]
HGNC gene
- cytochrome P450 family 26 subfamily B member 1 [HGNC gene]
NCIt concept(s)
- CYP26B1 Gene [NCIt concept]
- CYP26B1 wt Allele [NCIt concept]
- Cytochrome P450 26B1 [NCIt concept]
ORDO concept(s)
- cytochrome P450 family 26 subfamily B member 1 [ORDO Gene]
Phenotypes related
- Radiohumeral fusions with other skeletal and craniofacial anomalies [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- CYP26B1 Gene [NCIt concept]
- cytochrome P450 family 26 subfamily B member 1 [HGNC gene]

Keyword's position in hierarchy(ies) :

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