Gene Expression: KCNQ1

Gene Data

  • Gene Symbol: KCNQ1
  • Gene ID: 3784
  • Synonyms: ATFB1, ATFB3, JLNS1, KCNA8, KCNA9, KVLQT1, Kv1.9, Kv7.1, LQT, LQT1, RWS, SQT2, WRS
  • Description: potassium voltage-gated channel, KQT-like subfamily, member 1
  • Database Refs: HGNC:6294, MIM:607542, Ensembl:ENSG00000053918, HPRD:06341, Vega:OTTHUMG00000009900
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 18 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters: No Clusters were found

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 39 diseases, scroll to view all:
  1. Auditory system disease
  2. Beckwith-Wiedemann syndrome
  3. Brugada syndrome
  4. Carbohydrate metabolism disease
  5. Cardiovascular system disease
  6. Complex genetic disease
  7. Congenital heart block
  8. Congenital heart defect
  9. Cystic fibrosis
  10. Diabetes mellitus
  11. Disease
  12. Disease of anatomical entity
  13. Disease of metabolism
  14. Endocrine pancreas disease
  15. Endocrine system disease
  16. Episodic ataxia
  17. Familial atrial fibrillation
  18. Familial periodic paralysis
  19. Gastrointestinal system disease
  20. Genetic disease
  21. Genetic disorder
  22. Glucose metabolism disease
  23. Heart disease
  24. Hyperkalemic periodic paralysis
  25. Hypertrophic cardiomyopathy
  26. Hypokalemia
  27. Inner ear disease
  28. Intrinsic cardiomyopathy
  29. Jervell-Lange Nielsen syndrome
  30. Long QT syndrome
  31. Medical disorder
  32. Monogenic disease
  33. Pancreas disease
  34. Physical disorder
  35. Sensorineural hearing loss
  36. Sick sinus syndrome
  37. Subclavian steal syndrome
  38. Sudden infant death syndrome
  39. Syndrome

Stage Associations

This gene is associated with the following stages: No Stages were found