ATP binding cassette subfamily B member 7

Preferred Label : ATP binding cassette subfamily B member 7;

Approved symbol HGNC : ABCB7;

Alias symbols HGNC : Atm1p; ASAT; EST140535;

Chromosome HGNC : Xq13.3;

Locus type HGNC : protein-coding gene;

Ensembl Id : ENSG00000131269;

Details

Origin ID

HGNC:48;

UMLS CUI

C1412073;

Automatic exact mappings (from CISMeF team)
- ATP binding cassette subfamily B member 7 [ORDO Gene]
- Atp-binding cassette, subfamily b, member 7 [OMIM gene]
- Spinocerebellar ataxia, X-linked 6, with or without sideroblastic anemia [OMIM Phenotype]
OMIM gene
- Atp-binding cassette, subfamily b, member 7 [OMIM gene]
Orphanet gene
- ATP binding cassette subfamily B member 7 [ORDO Gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- Atp-binding cassette, subfamily b, member 7 [OMIM gene]

Keyword's position in hierarchy(ies) :

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