Gene Expression: OPA1

Gene Data

  • Gene Symbol: OPA1
  • Gene ID: 4976
  • Synonyms: MGM1, NPG, NTG, largeG
  • Description: optic atrophy 1 (autosomal dominant)
  • Database Refs: HGNC:8140, MIM:605290, Ensembl:ENSG00000198836, HPRD:05596, Vega:OTTHUMG00000149897
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 31 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 26 diseases, scroll to view all:
  1. Acute orbital inflammation
  2. Blue color blindness
  3. Central nervous system disease
  4. Cranial nerve disease
  5. Disease
  6. Disease of anatomical entity
  7. Eye and adnexa disease
  8. Eye disease
  9. Glaucoma
  10. Globe disease
  11. Leber hereditary optic neuropathy
  12. Low tension glaucoma
  13. Nervous system disease
  14. Neurodegenerative disease
  15. Neuropathy
  16. open-angle glaucoma
  17. Optic atrophy
  18. Optic nerve disease
  19. Orbital cellulitis
  20. Primary open anle glaucoma
  21. Retinal degeneration
  22. Sensorineural hearing loss
  23. Sensory system disease
  24. Tauopathy
  25. Usher syndrome
  26. Visual pathway disease

Stage Associations

This gene is associated with the following stages: