Gene Expression: OPA3

Gene Data

  • Gene Symbol: OPA3
  • Gene ID: 80207
  • Synonyms: MGA3
  • Description: optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
  • Database Refs: HGNC:8142, MIM:606580, Ensembl:ENSG00000125741, HPRD:05956, Vega:OTTHUMG00000182125
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 4 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters:

Disease Associations

This gene is associated with the following diseases. Clicking on the disease will take you to the disease association entry for that disease.

This gene is associated with 24 diseases, scroll to view all:
  1. angle-closure glaucoma
  2. Barth syndrome
  3. Congenital nystagmus
  4. Cranial nerve disease
  5. Eye and adnexa disease
  6. Eye disease
  7. Friedreich ataxia
  8. Globe disease
  9. Inner ear disease
  10. Ischemic optic neuropathy
  11. Leber hereditary optic neuropathy
  12. Mitochondrial disease
  13. Nervous system disease
  14. Neuropathy
  15. Ocular motility disease
  16. Optic atrophy
  17. Optic nerve disease
  18. Optic neuritis
  19. Pathologic nystagmus
  20. Primary angle-closure glaucoma
  21. Sensorineural hearing loss
  22. Sensory system disease
  23. Visual pathway disease
  24. Wolfram syndrome

Stage Associations

This gene is associated with the following stages: