Gene Expression: SCN8A

Gene Data

  • Gene Symbol: SCN8A
  • Gene ID: 6334
  • Synonyms: CERIII, CIAT, EIEE13, MED, NaCh6, Nav1.6, PN4
  • Description: sodium channel, voltage gated, type VIII, alpha subunit
  • Database Refs: HGNC:10596, MIM:600702, Ensembl:ENSG00000196876, HPRD:09006, Vega:OTTHUMG00000169490
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 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 41 diseases, scroll to view all:
  1. Absence epilepsy
  2. Benign familial neonatal convulsion
  3. Benign neonatal epilepsy
  4. Brain disease
  5. Brugada syndrome
  6. Central nervous system disease
  7. Chikungunya
  8. Complex genetic disease
  9. Congenital myasthenic syndrome
  10. Diabetic neuropathy
  11. Disease
  12. Disease by infectious agent
  13. Disease of anatomical entity
  14. Epilepsy
  15. Episodic ataxia
  16. Erythromelalgia
  17. Familial periodic paralysis
  18. Generalized epilepsy
  19. Genetic disease
  20. Hereditary sensory neuropathy
  21. Hyperkalemic periodic paralysis
  22. Hypokalemic periodic paralysis
  23. Intractable epilepsy
  24. Juvenile absence epilepsy
  25. Long QT syndrome
  26. Malaria
  27. Migraine
  28. Muscle tissue disease
  29. Muscular disease
  30. Musculoskeletal system disease
  31. Myopathy
  32. Nervous system disease
  33. Neurodegenerative disease
  34. Neuromuscular disease
  35. Neuropathy
  36. Parasitic infectious disease
  37. Parasitic protozoa infectious disease
  38. Partial epilepsy
  39. Peripheral neuropathy
  40. Peripheral vascular disease
  41. Thomsen disease

Stage Associations

This gene is associated with the following stages: