Gene Expression: NPPA

Gene Data

  • Gene Symbol: NPPA
  • Gene ID: 4878
  • Synonyms: ANF, ANP, ATFB6, CDD-ANF, PND
  • Description: natriuretic peptide A
  • Database Refs: HGNC:7939, MIM:108780, Ensembl:ENSG00000175206, HPRD:00164, Vega:OTTHUMG00000002388
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 3 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 105 diseases, scroll to view all:
  1. Acute kidney failure
  2. Acute kidney tubular necrosis
  3. Acute myocardial infarction
  4. Adrenal cortex disease
  5. Adrenal gland disease
  6. Adrenal gland hyperfunction
  7. Aortic valve disease
  8. Aortic valve insufficiency
  9. Aortic valve stenosis
  10. Arteriopathy
  11. Atrial heart septal defect
  12. Bartter disease
  13. Brain disease
  14. Brain edema
  15. Carbohydrate metabolism disease
  16. Cardiac tamponade
  17. Cardiovascular system disease
  18. Central nervous system disease
  19. Cerebrovascular accident
  20. Cerebrovascular disease
  21. Chronic kidney failure
  22. Chronic obstructive pulmonary disease
  23. Chronic pulmonary heart disease
  24. Congenital heart block
  25. Congenital heart defect
  26. Congestive heart failure
  27. Conn syndrome
  28. Constrictive pericarditis
  29. Cor pulmonale
  30. Coronary heart disease
  31. Diabetes insipidus
  32. Diabetes mellitus
  33. Diastolic heart failure
  34. Dilated cardiomyopathy
  35. Disease
  36. Disease of anatomical entity
  37. Disease of cellular proliferation
  38. Disease of metabolism
  39. End stage renal failure
  40. Endocrine pancreas disease
  41. Endocrine syndrome
  42. Endocrine system disease
  43. Essential hypertension
  44. Extrinsic cardiomyopathy
  45. Familial atrial fibrillation
  46. Gastrointestinal system disease
  47. Glomerulonephritis
  48. Glucose metabolism disease
  49. Heart disease
  50. Heart failure
  51. Heart septal defect
  52. Heart valve disease
  53. Hepatobiliary disease
  54. Hepatorenal syndrome
  55. Hyperaldosteronism
  56. Hyperglycemia
  57. Hypertension
  58. Hypertrophic cardiomyopathy
  59. Inappropriate ADH syndrome
  60. Inborn errors renal tubular transport
  61. Intracranial hypertension
  62. Intrinsic cardiomyopathy
  63. Ischemia
  64. Kidney disease
  65. Kidney failure
  66. Liver cirrhosis
  67. Liver disease
  68. Lower respiratory tract disease
  69. Lung disease
  70. Medical disorder
  71. Mitral valve disease
  72. Mitral valve insufficiency
  73. Mitral valve stenosis
  74. Myocardial infarction
  75. Myocardial ischemia
  76. Myocarditis
  77. Nephritis
  78. Nephrosis
  79. Nephrotic syndrome
  80. Nervous system disease
  81. Newborn respiratory distress syndrome
  82. Obstructive lung disease
  83. Pancreas disease
  84. Patent ductus arteriosus
  85. Pericardial effusion
  86. Persistent fetal circulation syndrome
  87. Physical disorder
  88. Polyhydramnios
  89. pre-eclampsia
  90. Primary pulmonary hypertension
  91. Proteinuria
  92. Pulmonary edema
  93. Pulmonary hypertension
  94. Renal hypertension
  95. Renovascular hypertension
  96. Respiratory failure
  97. Respiratory system disease
  98. Rheumatic disease of mitral valve
  99. Secondary hypertension
  100. Sick sinus syndrome
  101. Tetralogy of Fallot
  102. Thyroid gland disease
  103. Urinary system disease
  104. Vascular disease
  105. Ventricular septal defect

Stage Associations

This gene is associated with the following stages: