Gene Expression: MYH9

Gene Data

  • Gene Symbol: MYH9
  • Gene ID: 4627
  • Synonyms: BDPLT6, DFNA17, EPSTS, FTNS, MHA, NMHC-II-A, NMMHC-IIA, NMMHCA
  • Description: myosin, heavy chain 9, non-muscle
  • Database Refs: HGNC:7579, MIM:160775, Ensembl:ENSG00000100345, HPRD:01177, Vega:OTTHUMG00000030429
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 4 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 36 diseases, scroll to view all:
  1. Alport syndrome
  2. Auditory system disease
  3. Bernard-Soulier syndrome
  4. Blood coagulation disease
  5. Blood platelet disease
  6. Cardiovascular system disease
  7. Chronic kidney failure
  8. Cleft lip
  9. Disease
  10. Disease of anatomical entity
  11. End stage renal failure
  12. Focal segmental glomerulosclerosis
  13. Glomerulonephritis
  14. Hematopoietic system disease
  15. Hemorrhagic disease
  16. Hypertension
  17. Inherited blood coagulation disease
  18. Inner ear disease
  19. Kidney disease
  20. Kidney failure
  21. Monogenic disease
  22. Nephritis
  23. Nephrosclerosis
  24. Nervous system disease
  25. Nonsyndromic deafness
  26. Proteinuria
  27. Renal hypertension
  28. Renal vascular disease
  29. Secondary hypertension
  30. Sensorineural hearing loss
  31. Sensory system disease
  32. Thrombocytopenia
  33. Thrombocytopenia due to platelet alloimm
  34. Urinary system disease
  35. Vascular disease
  36. Wiskott-Aldrich syndrome

Stage Associations

This gene is associated with the following stages: