CYP2U1 wt Allele

Preferred Label : CYP2U1 wt Allele;

NCIt synonyms : SPG49; Cytochrome P450 Family 2 Subfamily U Member 1 wt Allele; P450TEC; Cytochrome P450, Family 2, Subfamily U, Polypeptide 1 Gene; Spastic Paraplegia 49 Gene; Spastic Paraplegia 56 (Autosomal Recessive) Gene; SPG56;

NCIt definition : Human CYP2U1 wild-type allele is located in the vicinity of 4q25 and is approximately 22 kb in length. This allele, which encodes cytochrome P450 2U1 protein, is involved in the oxidation of arachidonic acid and its conjugates. Mutation of the gene is associated with autosomal recessive spastic paraplegia 56.;

NCI Metathesaurus CUI : CL1907133;

GenBank Accession Number : BC012027;

Details

Origin ID

C200321;

UMLS CUI

C5849091;

OMIM relation
- Cytochrome p450, family 2, subfamily u, polypeptide 1 [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 4q25 [NCIt concept]
gene_is_element_in_pathway
- Arachidonic Acid Metabolism Pathway [NCIt concept]
- Fatty Acid Metabolism Pathway [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]
- Xenobiotic Metabolism [NCIt concept]

Keyword's position in hierarchy(ies) :

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