Gene Expression: CACNA1S

Gene Data

  • Gene Symbol: CACNA1S
  • Gene ID: 779
  • Synonyms: CACNL1A3, CCHL1A3, Cav1.1, HOKPP, HOKPP1, MHS5, TTPP1, hypoPP
  • Description: calcium channel, voltage-dependent, L type, alpha 1S subunit
  • Database Refs: HGNC:1397, MIM:114208, Ensembl:ENSG00000081248, HPRD:00248, Vega:OTTHUMG00000035784
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 44 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 29 diseases, scroll to view all:
  1. Atrophic muscular disease
  2. Central core myopathy
  3. Congenital structural myopathy
  4. Disease
  5. Disease of anatomical entity
  6. Disease of metabolism
  7. Endocrine syndrome
  8. Endocrine system disease
  9. Familial periodic paralysis
  10. Hyperkalemic periodic paralysis
  11. Hypokalemia
  12. Hypokalemic periodic paralysis
  13. Inborn errors metal metabolism
  14. Lambert-Eaton myasthenic syndrome
  15. limb-girdle muscular dystrophy
  16. Malignant hyperthermia
  17. Mineral metabolism disease
  18. Muscle tissue disease
  19. Muscular disease
  20. Muscular dystrophy
  21. Musculoskeletal system disease
  22. Myopathy
  23. Myopathy of critical illness
  24. Myotonic disease
  25. Neuromuscular disease
  26. Neuromuscular junction disease
  27. Neuropathy
  28. Quadriplegia
  29. Thomsen disease

Stage Associations

This gene is associated with the following stages: