History:GENE:AAAS    

Gene Expression: KCNJ13

Gene Data

  • Gene Symbol: KCNJ13
  • Gene ID: 3769
  • Synonyms: KIR1.4, KIR7.1, LCA16, SVD
  • Description: potassium inwardly-rectifying channel, subfamily J, member 13
  • Database Refs: HGNC:6259, MIM:603208, Ensembl:ENSG00000115474, HPRD:04441, Vega:OTTHUMG00000153292
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 6 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 27 diseases, scroll to view all:
  1. Arteriopathy
  2. Atrial heart septal defect
  3. Benign paroxysmal positional nystagmus
  4. Brain disease
  5. Cardiovascular system disease
  6. Central nervous system disease
  7. Cerebrovascular accident
  8. Cerebrovascular disease
  9. Congenital heart defect
  10. Disease
  11. Disease of anatomical entity
  12. Endocarditis
  13. Extrinsic cardiomyopathy
  14. Heart disease
  15. Heart septal defect
  16. Intracranial arteriosclerosis
  17. Ischemia
  18. Myocardial ischemia
  19. Nervous system disease
  20. Psychophysiologic disease
  21. Retrocochlear disease
  22. Somatoform disease
  23. Splenic infarction
  24. Vascular dementia
  25. Vascular disease
  26. Vestibular neuronitis
  27. Vestibulocochlear nerve disease

Stage Associations

This gene is associated with the following stages: