Gene Expression: NOS3

Gene Data

  • Gene Symbol: NOS3
  • Gene ID: 4846
  • Synonyms: ECNOS, eNOS
  • Description: nitric oxide synthase 3 (endothelial cell)
  • Database Refs: HGNC:7876, MIM:163729, Ensembl:ENSG00000164867, HPRD:01224, Vega:OTTHUMG00000158343
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 8 out of 30 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 107 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. Alzheimer's disease
  3. Aneurysm
  4. Aortic valve disease
  5. Aortic valve stenosis
  6. Arterial occlusive disease
  7. Arteriopathy
  8. Arteriosclerosis
  9. Arteriosclerotic cardiovascular disease
  10. Asthma
  11. Atherosclerosis
  12. Brain disease
  13. Brain edema
  14. Brain hypoxia-Ischemia
  15. Brain infarction
  16. Brain ischemia
  17. Bronchial disease
  18. Cancer
  19. Carbohydrate metabolism disease
  20. Cardiovascular system disease
  21. Central nervous system disease
  22. Cerebral artery occlusion
  23. Cerebral infarction
  24. Cerebrovascular accident
  25. Cerebrovascular disease
  26. Chronic kidney failure
  27. Chronic myocardial ischemia
  28. Cognitive disease
  29. Congenital diaphragmatic hernia
  30. Congestive heart failure
  31. Coronary arteriosclerosis
  32. Coronary artery vasospasm
  33. Coronary heart disease
  34. Dementia
  35. Diabetes mellitus
  36. Diabetic retinopathy
  37. Disease
  38. Disease of anatomical entity
  39. Disease of cellular proliferation
  40. Disease of mental health
  41. Disease of metabolism
  42. End stage renal failure
  43. Endocrine pancreas disease
  44. Endocrine system disease
  45. Essential hypertension
  46. Extrinsic cardiomyopathy
  47. Eye and adnexa disease
  48. Eye disease
  49. Gastrointestinal system disease
  50. Globe disease
  51. Glucose metabolism disease
  52. Heart disease
  53. Heart failure
  54. Hepatic vascular disease
  55. Hepatobiliary disease
  56. Hepatopulmonary syndrome
  57. Hypercholesterolemia
  58. Hyperglycemia
  59. Hyperhomocysteinemia
  60. Hyperinsulinism
  61. Hypertension
  62. Impotence
  63. Inborn errors of amino acid metabolism
  64. Inborn errors of metabolism
  65. Ischemia
  66. Kidney disease
  67. Kidney failure
  68. Lipid metabolism disease
  69. Liver cirrhosis
  70. Liver disease
  71. Lower respiratory tract disease
  72. Lung disease
  73. Male reproductive system disease
  74. Migraine
  75. Musculoskeletal system disease
  76. Myocardial infarction
  77. Myocardial ischemia
  78. Nervous system disease
  79. Neurodegenerative disease
  80. Obstructive lung disease
  81. Organ system cancer
  82. Pancreas disease
  83. Penile disease
  84. Persistent fetal circulation syndrome
  85. Portal hypertension
  86. pre-eclampsia
  87. Proteinuria
  88. Pulmonary edema
  89. Pulmonary hypertension
  90. Reproductive system disease
  91. Respiratory failure
  92. Respiratory system disease
  93. Retinal disease
  94. Retinal vascular disease
  95. Sensory system disease
  96. Sexual disease
  97. Sexual dysfunction
  98. Spermatic cord torsion
  99. Tauopathy
  100. Testicular disease
  101. Thromboangiitis obliterans
  102. Toxic encephalopathy
  103. Ureteral disease
  104. Ureteral obstruction
  105. Urinary system disease
  106. Urinary tract obstruction
  107. Vascular disease

Stage Associations

This gene is associated with the following stages: