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Gene : SLC25A4 Homo sapiens

Name  ? solute carrier family 25 member 4 Cytological Location  4q35.1
Brief Description  solute carrier family 25 member 4
description  This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013]
  • synonyms:
  • AAC1,
  • PEO3,
  • NM_001151,
  • SLC25A4,
  • T1,
  • ANT 1,
  • ANT,
  • PEO2,
  • ANT1,
  • uc003ixd.4,
  • PEO3,
  • OTTHUMG00000134299,
  • HGNC:10990,
  • ANT1,
  • solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 4,
  • MTDPS12,
  • PEO2,
  • PEOA2,
  • MTDPS12A,
  • BC008664,
  • T1
  • identifiers:
  • 291,
  • ENSG00000151729,
  • SLC25A4

Genome feature

Region: gene ? Length: 7117  
Location: 4:185143266-185150382 Cyto location: 4q35.1

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Chromosomal location.

Gene --> GO terms.

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Gene --> Proteins.


Gene Report --> GWAS hit


3 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


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Gene --> Orthologues


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Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



385 SN Ps

5 Cross References

19 Data Sets

18 Homologues

0 Located Features

97 Rna Seq Results