History:GENE:MS4A6E    GENE:NUTM2A    GENE:GABRA6    GENE:PSTPIP1    GENE:MAGEA12    

Gene Expression: KCNMA1

Gene Data

  • Gene Symbol: KCNMA1
  • Gene ID: 3778
  • Synonyms: BKTM, KCa1.1, MaxiK, SAKCA, SLO, SLO-ALPHA, SLO1, bA205K10.1, mSLO1
  • Description: potassium large conductance calcium-activated channel, subfamily M, alpha member 1
  • Database Refs: HGNC:6284, MIM:600150, Ensembl:ENSG00000156113, HPRD:15967, Vega:OTTHUMG00000018543
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 44 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 28 diseases, scroll to view all:
  1. Bartter disease
  2. Brain disease
  3. Cardiovascular system disease
  4. Central nervous system disease
  5. Cerebrovascular accident
  6. Cerebrovascular disease
  7. Colonic disease
  8. Colonic pseudo-obstruction
  9. Coronary artery vasospasm
  10. Diabetes mellitus
  11. Disease
  12. Disease of anatomical entity
  13. Disease of metabolism
  14. Endocrine pancreas disease
  15. Endocrine system disease
  16. Functional colonic disease
  17. Gastrointestinal system disease
  18. Glaucoma
  19. Hypertension
  20. Hypokalemia
  21. Inborn errors renal tubular transport
  22. Ischemia
  23. Nervous system disease
  24. Ovary serous adenocarcinoma
  25. Pancreas disease
  26. Pseudohypoaldosteronism
  27. Toxic megacolon
  28. Vascular disease

Stage Associations

This gene is associated with the following stages: