Gene Expression: KCNJ1

Gene Data

  • Gene Symbol: KCNJ1
  • Gene ID: 3758
  • Synonyms: KIR1.1, ROMK, ROMK1
  • Description: potassium inwardly-rectifying channel, subfamily J, member 1
  • Database Refs: HGNC:6255, MIM:600359, Ensembl:ENSG00000151704, HPRD:08981, Vega:OTTHUMG00000048247
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 5 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 32 diseases, scroll to view all:
  1. Adrenal cortex disease
  2. Adrenal gland disease
  3. Adrenal gland hyperfunction
  4. Bartter disease
  5. Calcinosis
  6. Calcium metabolism disease
  7. Cardiovascular system disease
  8. Disease
  9. Disease of anatomical entity
  10. Disease of metabolism
  11. Endocrine system disease
  12. Familial juvenile hyperuricemic nephropa
  13. Female reproductive system disease
  14. Gitelman syndrome
  15. Hydronephrosis
  16. Hyperaldosteronism
  17. Hypertension
  18. Hypokalemia
  19. Inborn errors of metabolism
  20. Inborn errors renal tubular transport
  21. Inner ear disease
  22. Kidney disease
  23. Mineral metabolism disease
  24. Nephrocalcinosis
  25. Nephrogenic diabetes insipidus
  26. Nephrolithiasis
  27. Polyhydramnios
  28. Pregnancy disease
  29. Pseudohypoaldosteronism
  30. Sensorineural hearing loss
  31. Urinary system disease
  32. Vascular disease

Stage Associations

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