Solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4

Preferred Label : Solute carrier family 25 (mitochondrial carrier, adenine nucleotide translocator), member 4;

Symbol : SLC25A4;

CISMeF acronym : SLC25A4;

Type : Gene;

Alternative titles and symbols : Adenine nucleotide translocator 1; Adp/atp translocator of skeletal muscle; Adp/atp translocase 1; Adp/atp carrier 1; ANT1; ANT; AAC1;

Ensembl ID : ENSG00000151729;

Prefixed ID : *103220;

Details

Origin ID

103220;

UMLS CUI

C1335833;

Automatic exact mappings (from CISMeF team)
- ADP/ATP Translocase 1 [NCIt concept]
- Adenosine Nucleotide Transporter [NCIt concept]
- Ant [ICD-11 Extension code]
- NAT1 wt Allele [NCIt concept]
- SLC25A4 Gene [NCIt concept]
- SLC25A4 gene [LOINC component]
- SLC25A4 wt Allele [NCIt concept]
- adenine nucleotide translocator 1 [MeSH concept]
- adenine nucleotide translocator 1 [MeSH Descriptor]
- ants [MeSH Descriptor]
- pre-mRNA processing factor 6 [ORDO Gene]
- solute carrier family 25 member 4 [HGNC gene]
- solute carrier family 25 member 4 [ORDO Gene]
HGNC gene
- solute carrier family 25 member 4 [HGNC gene]
NCIt concept(s)
- ADP/ATP Translocase 1 [NCIt concept]
- SLC25A4 Gene [NCIt concept]
- SLC25A4 wt Allele [NCIt concept]
ORDO concept(s)
- solute carrier family 25 member 4 [ORDO Gene]
Phenotypes related
- Mitochondrial dna depletion syndrome 12a (cardiomyopathic type), autosomal dominant [OMIM Phenotype]
- Mitochondrial dna depletion syndrome 12b (cardiomyopathic type), autosomal recessive [OMIM Phenotype]
- Progressive external ophthalmoplegia with mitochondrial dna deletions, autosomal dominant 2 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- SLC25A4 Gene [NCIt concept]
- SLC25A4 gene [LOINC component]
- solute carrier family 25 member 4 [HGNC gene]

Keyword's position in hierarchy(ies) :

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