Gene Expression: SCN1B

Gene Data

  • Gene Symbol: SCN1B
  • Gene ID: 6324
  • Synonyms: ATFB13, BRGDA5, GEFSP1
  • Description: sodium channel, voltage-gated, type I, beta subunit
  • Database Refs: HGNC:10586, MIM:600235, Ensembl:ENSG00000105711, HPRD:02581, Vega:OTTHUMG00000182472
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 8 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 27 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. Complex genetic disease
  8. Conduction disease
  9. Disease
  10. Disease of anatomical entity
  11. Epilepsy
  12. Familial periodic paralysis
  13. Generalized epilepsy
  14. Genetic disease
  15. Hyperkalemic periodic paralysis
  16. Infantile epileptic encephalopathy
  17. Long QT syndrome
  18. Muscle tissue disease
  19. Muscular disease
  20. Musculoskeletal system disease
  21. Myopathy
  22. Nervous system disease
  23. Neuromuscular disease
  24. Neuropathy
  25. Partial epilepsy
  26. Unverricht-Lundborg syndrome
  27. West syndrome

Stage Associations

This gene is associated with the following stages: