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Gene Expression: KCNJ12

Gene Data

  • Gene Symbol: KCNJ12
  • Gene ID: 3768
  • Synonyms: IRK-2, IRK2, KCNJN1, Kir2.2, Kir2.2v, hIRK, hIRK1, hkir2.2x, kcnj12x
  • Description: potassium inwardly-rectifying channel, subfamily J, member 12
  • Database Refs: HGNC:6258, MIM:602323, Ensembl:ENSG00000184185, HPRD:09083, Vega:OTTHUMG00000132039
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 4 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 25 diseases, scroll to view all:
  1. Calcinosis
  2. Carbohydrate metabolism disease
  3. Diabetes mellitus
  4. Disease
  5. Disease of anatomical entity
  6. Disease of metabolism
  7. Endocrine pancreas disease
  8. Endocrine system disease
  9. Familial periodic paralysis
  10. Gastrointestinal system disease
  11. Gitelman syndrome
  12. Glucose metabolism disease
  13. Hyperinsulinemic hypoglycemia
  14. Hyperinsulinism
  15. Hypoglycemia
  16. Hypokalemia
  17. Hypokalemic periodic paralysis
  18. Inborn errors carbohydrate metabolism
  19. Lens subluxation
  20. Long QT syndrome
  21. Mineral metabolism disease
  22. Neonatal diabetes mellitus
  23. Nephrocalcinosis
  24. Pancreas disease
  25. Polyhydramnios

Stage Associations

This gene is associated with the following stages: