Disease Annotation

Gene Info

  • Species: Human (Homo sapiens)
  • GeneID: 4976
  • Symbol: OPA1
  • Description: OPA1 mitochondrial dynamin like GTPase

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Disease_Term Source Rank Other Values
?Mitochondrial DNA depletion syndrome 14 (encephalocardiomyopathic type), 616896 (3) OMIM high
  • Genome region : 3q29
  • OMIM_ID : 605290 OMIM gene ID
  • OMIM_ID : 616896 OMIM phenotype ID
Optic atrophy 1, 165500 (3) OMIM high
  • Genome region : 3q29
  • OMIM_ID : 165500 OMIM phenotype ID
  • OMIM_ID : 605290 OMIM gene ID
{Glaucoma, normal tension, susceptibility to}, 606657 (3) OMIM high
  • Genome region : 10p13
  • Genome region : 3q29
  • OMIM_ID : 602432 OMIM gene ID
  • OMIM_ID : 605290 OMIM gene ID
  • OMIM_ID : 606657 OMIM phenotype ID
Optic atrophy plus syndrome, 125250 (3) OMIM high
  • Genome region : 3q29
  • OMIM_ID : 125250 OMIM phenotype ID
  • OMIM_ID : 605290 OMIM gene ID
Behr syndrome, 210000 (3) OMIM high
  • Genome region : 3q29
  • OMIM_ID : 210000 OMIM phenotype ID
  • OMIM_ID : 605290 OMIM gene ID