Gene Expression: KCNJ2

Gene Data

  • Gene Symbol: KCNJ2
  • Gene ID: 3759
  • Synonyms: ATFB9, HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7, SQT3
  • Description: potassium inwardly-rectifying channel, subfamily J, member 2
  • Database Refs: HGNC:6263, MIM:600681, Ensembl:ENSG00000123700, HPRD:02815, Vega:OTTHUMG00000180351
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 3 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 23 diseases, scroll to view all:
  1. Anderson-Tawil syndrome
  2. Brugada syndrome
  3. Cardiovascular system disease
  4. Complex genetic disease
  5. Disease
  6. Disease of anatomical entity
  7. Familial atrial fibrillation
  8. Familial periodic paralysis
  9. Genetic disease
  10. Heart disease
  11. Heart failure
  12. Hyperkalemic periodic paralysis
  13. Hypokalemia
  14. Hypokalemic periodic paralysis
  15. Inborn errors metal metabolism
  16. Long QT syndrome
  17. Mineral metabolism disease
  18. Muscle tissue disease
  19. Muscular disease
  20. Musculoskeletal system disease
  21. Myopathy
  22. Syndactyly
  23. Tetanus

Stage Associations

This gene is associated with the following stages: