Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 291
  • Symbol: SLC25A4
  • Description: solute carrier family 25 member 4

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Disease_Term Source Rank Other Values
Mitochondrial DNA depletion syndrome 12A (cardiomyopathic type) AD, 617184 (3) OMIM high
  • Genome region : 4q35.1
  • OMIM_ID : 103220 OMIM gene ID
  • OMIM_ID : 617184 OMIM phenotype ID
Mitochondrial DNA depletion syndrome 12B (cardiomyopathic type) AR, 615418 (3) OMIM high
  • Genome region : 4q35.1
  • OMIM_ID : 103220 OMIM gene ID
  • OMIM_ID : 615418 OMIM phenotype ID
Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 2, 609283 (3) OMIM high
  • Genome region : 4q35.1
  • OMIM_ID : 103220 OMIM gene ID
  • OMIM_ID : 609283 OMIM phenotype ID