CYP4V2 wt Allele

Preferred Label : CYP4V2 wt Allele;

NCIt synonyms : Cytochrome P450 Family 4 Subfamily V Member 2 wt Allele; CYP4AH1; Cytochrome P450, Family 4, Subfamily V, Polypeptide 2 Gene; BCD;

NCIt definition : Human CYP4V2 wild-type allele is located within 4q35.1-q35.2 and is approximately 22 kb in length. This allele, which encodes cytochrome P450 4V2 protein, plays a role in the metabolism of saturated fatty acids. Mutation of the gene is associated with Bietti crystalline corneoretinal dystrophy.;

NCI Metathesaurus CUI : CL1907136;

GenBank Accession Number : AK022114;

Détails

Origin ID

C200329;

UMLS CUI

C5849073;

OMIM relation
- Cytochrome p450, family 4, subfamily V, polypeptide 2 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_plays_role_in_process
- Detoxification [NCIt concept]
- Fatty Acid Metabolism [NCIt concept]
- Intermediary Metabolic Process [NCIt concept]
- Iron Chelation [NCIt concept]
- Oxidation [NCIt concept]
- Oxidation/Reduction [NCIt concept]
- Visual Perception [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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