History:GENE:CLRN1    

Gene Expression: KCNJ10

Gene Data

  • Gene Symbol: KCNJ10
  • Gene ID: 3766
  • Synonyms: BIRK-10, KCNJ13-PEN, KIR1.2, KIR4.1, SESAME
  • Description: potassium inwardly-rectifying channel, subfamily J, member 10
  • Database Refs: HGNC:6256, MIM:602208, Ensembl:ENSG00000177807, HPRD:03732, Vega:OTTHUMG00000024073
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 2 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 34 diseases, scroll to view all:
  1. Auditory system disease
  2. Brain disease
  3. Brain edema
  4. Central nervous system disease
  5. Central retinal vein occlusion
  6. Developmental disease of mental health
  7. Diabetic retinopathy
  8. Disease
  9. Disease of anatomical entity
  10. Enlarged vestibular aqueduct
  11. Epilepsy
  12. Eye and adnexa disease
  13. Eye disease
  14. Generalized epilepsy
  15. Globe disease
  16. Hypervitaminosis D
  17. Inner ear disease
  18. Intellectual disability
  19. Muscle tissue disease
  20. Muscular disease
  21. Myopathy
  22. Nervous system disease
  23. Neuromuscular disease
  24. Neuropathy
  25. Nonsyndromic deafness
  26. Retinal degeneration
  27. Retinal detachment
  28. Retinal disease
  29. Retinal edema
  30. Retinal vascular disease
  31. Retinal vascular occlusion
  32. Sensorineural hearing loss
  33. Sensory system disease
  34. Specific developmental disease

Stage Associations

This gene is associated with the following stages: