cytochrome P450 family 2 subfamily U member 1

Preferred Label : cytochrome P450 family 2 subfamily U member 1;

Approved symbol HGNC : CYP2U1;

Name synonyms HGNC : spastic paraplegia 49;

Alias symbols HGNC : SPG49;

Chromosome HGNC : 4q25;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000155016;

Details

Origin ID

HGNC:20582;

UMLS CUI

C1427016;

Automatic exact mappings (from CISMeF team)
- Cytochrome p450, family 2, subfamily u, polypeptide 1 [OMIM gene]
- Neuropathy, hereditary sensory and autonomic, type ix, with developmental delay [OMIM Phenotype]
- cytochrome P450 family 2 subfamily U member 1 [ORDO Gene]
NCIt concept
- CYP2U1 Gene [NCIt concept]
OMIM gene
- Cytochrome p450, family 2, subfamily u, polypeptide 1 [OMIM gene]
Orphanet gene
- cytochrome P450 family 2 subfamily U member 1 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Cytochrome p450, family 2, subfamily u, polypeptide 1 [OMIM gene]

Keyword's position in hierarchy(ies) :

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