CYP26B1 wt Allele

Preferred Label : CYP26B1 wt Allele;

NCIt synonyms : P450RAI-2; Cytochrome P450, Family 26, Subfamily B, Polypeptide 1 wt Allele; RHFCA; P450RAI2; CYP26A2; P450, Retinoic Acid-Inactivating, 2 Gene; Cytochrome P450, Subfamily XXVIA, Polypeptide 2 Gene; Cytochrome P450, Subfamily XXVIB, Polypeptide 1 Gene;

NCIt definition : Human CYP26B1 wild-type allele is located in the vicinity of 2p13.2 and is approximately 19 kb in length. This allele, which encodes cytochrome P450 26B1 protein, is involved in the specific inactivation of all-trans-retinoic acid. Mutations in this gene are associated with craniofacial and other skeletal anomalies.;

GenBank Accession Number : NM_019885;

Details

Origin ID

C104875;

UMLS CUI

C3538839;

OMIM relation
- Cytochrome p450, subfamily xxvib, polypeptide 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
concept_is_in_subset
- CTRP Biomarker Terminology [NCIt concept]
- CTRP Molecular Genetic Biomarker Terminology [NCIt concept]
- CTRP Terminology [NCIt concept]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 2p13.2 [NCIt concept]
gene_is_element_in_pathway
- Retinol Metabolism Pathway [NCIt concept]
gene_plays_role_in_process
- Detoxification [NCIt concept]
- Intermediary Metabolic Process [NCIt concept]
- Iron Chelation [NCIt concept]
- Oxidation [NCIt concept]
- Oxidation/Reduction [NCIt concept]

Keyword's position in hierarchy(ies) :

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