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Gene Expression: KCNH2

Gene Data

  • Gene Symbol: KCNH2
  • Gene ID: 3757
  • Synonyms: ERG1, HERG, HERG1, Kv11.1, LQT2, SQT1
  • Description: potassium voltage-gated channel, subfamily H (eag-related), member 2
  • Database Refs: HGNC:6251, MIM:152427, Ensembl:ENSG00000055118, HPRD:01069, Vega:OTTHUMG00000158341
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 4 out of 18 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 44 diseases, scroll to view all:
  1. Amnestic disease
  2. Anterograde amnesia
  3. Autoimmune disease of the nervous system
  4. Benign familial neonatal convulsion
  5. Benign neonatal epilepsy
  6. Brain disease
  7. Brugada syndrome
  8. Cancer
  9. Cardiovascular system disease
  10. Central nervous system disease
  11. Complex genetic disease
  12. Congenital heart block
  13. Disease
  14. Disease of anatomical entity
  15. Disease of cellular proliferation
  16. Disease of mental health
  17. Encephalitis
  18. Epilepsy
  19. Episodic ataxia
  20. Familial atrial fibrillation
  21. Generalized epilepsy
  22. Genetic disease
  23. Heart disease
  24. Hypersensitivity reaction type II diseas
  25. Immune system cancer
  26. Jervell-Lange Nielsen syndrome
  27. Lambert-Eaton myasthenic syndrome
  28. Long QT syndrome
  29. Melanomatosis
  30. Muscle tissue disease
  31. Muscular disease
  32. Musculoskeletal system disease
  33. Myasthenia gravis
  34. Myopathy
  35. Nervous system disease
  36. Neuromuscular disease
  37. Neuromuscular junction disease
  38. Neuropathy
  39. Organ system cancer
  40. Stiff-Person syndrome
  41. Sudden infant death syndrome
  42. Syndrome
  43. Thymoma
  44. Thymus cancer

Stage Associations

This gene is associated with the following stages: