Gene Expression: SCN1A

Gene Data

  • Gene Symbol: SCN1A
  • Gene ID: 6323
  • Synonyms: EIEE6, FEB3, FEB3A, FHM3, GEFSP2, HBSCI, NAC1, Nav1.1, SCN1, SMEI
  • Description: sodium channel, voltage-gated, type I, alpha subunit
  • Database Refs: HGNC:10585, MIM:182389, Ensembl:ENSG00000144285, HPRD:01669, Vega:OTTHUMG00000044173
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 30 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 31 diseases, scroll to view all:
  1. Autism
  2. Autism spectrum disease
  3. Benign familial neonatal convulsion
  4. Benign neonatal epilepsy
  5. Brain disease
  6. Central nervous system disease
  7. Developmental disease of mental health
  8. Disease
  9. Disease of anatomical entity
  10. Disease of mental health
  11. Epilepsy
  12. Exanthema subitum
  13. Generalized epilepsy
  14. Hemiplegia
  15. Infantile epileptic encephalopathy
  16. Intellectual disability
  17. Intractable epilepsy
  18. Migraine
  19. Muscle tissue disease
  20. Muscular disease
  21. Musculoskeletal system disease
  22. Myopathy
  23. Nervous system disease
  24. Neuromuscular disease
  25. Neuropathy
  26. Partial epilepsy
  27. Pertussis
  28. Pervasive developmental disease
  29. Rolandic epilepsy
  30. Specific developmental disease
  31. West syndrome

Stage Associations

This gene is associated with the following stages: