Gene Expression: PIK3C2A

Gene Data

  • Gene Symbol: PIK3C2A
  • Gene ID: 5286
  • Synonyms: CPK, PI3-K-C2(ALPHA), PI3-K-C2A
  • Description: phosphatidylinositol-4-phosphate 3-kinase, catalytic subunit type 2 alpha
  • Database Refs: HGNC:8971, MIM:603601, Ensembl:ENSG00000011405, HPRD:04672, Vega:OTTHUMG00000166036
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 37 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 102 diseases, scroll to view all:
  1. Acute anterolateral myocardial infarctio
  2. Acute kidney tubular necrosis
  3. Acute myocardial infarction
  4. Acute myocarditis
  5. Aneurysm
  6. Anteroseptal myocardial infarction
  7. Atrophic muscular disease
  8. Bacterial infectious disease
  9. Basal ganglia disease
  10. Blood coagulation disease
  11. Brain disease
  12. Carbohydrate metabolism disease
  13. Cardiovascular system disease
  14. Central nervous system disease
  15. Central nervous system hereditary degene
  16. Cerebrovascular accident
  17. Cerebrovascular disease
  18. Childhood schizophrenia
  19. Commensal bacterial infectious disease
  20. Compartment syndrome
  21. Congestive heart failure
  22. Connective tissue disease
  23. Coronary heart disease
  24. Dermatitis
  25. Dermatomyositis
  26. Diabetes mellitus
  27. Diarrhea
  28. Disease
  29. Disease by infectious agent
  30. Disease of anatomical entity
  31. Disease of mental health
  32. Disease of metabolism
  33. Duchenne muscular dystrophy
  34. Endocrine pancreas disease
  35. Endocrine syndrome
  36. Endocrine system disease
  37. Eosinophilia
  38. Extrinsic cardiomyopathy
  39. Gas gangrene
  40. Gastrointestinal system disease
  41. Glucose metabolism disease
  42. Heart aneurysm
  43. Heart disease
  44. Heart failure
  45. Hematopoietic system disease
  46. Hemorrhagic disease
  47. Hypertension
  48. Hypokalemia
  49. Hypothyroidism
  50. Inferior myocardial infarction
  51. Influenza myositis
  52. Integumentary system disease
  53. Intermediate coronary syndrome
  54. Ischemia
  55. Kidney disease
  56. Kidney failure
  57. Legionellosis
  58. Legionnaires' disease
  59. Leptospirosis
  60. Leukocyte disease
  61. Lower respiratory tract disease
  62. Lung disease
  63. Malignant hyperthermia
  64. Mineral metabolism disease
  65. Mucinoses
  66. Muscle tissue disease
  67. Muscular atrophy
  68. Muscular disease
  69. Muscular dystrophy
  70. Musculoskeletal system disease
  71. Myocardial infarction
  72. Myocardial ischemia
  73. Myocarditis
  74. Myopathy
  75. Myositis
  76. Myotonic dystrophy
  77. Myxedema
  78. Nervous system disease
  79. Neuroleptic malignant syndrome
  80. Neuromuscular disease
  81. Neuropathy
  82. Ornithosis
  83. Pancreas disease
  84. Pericardial effusion
  85. Pericarditis
  86. Pneumonia
  87. Pneumopericardium
  88. Polycystic kidney disease
  89. Posteroinferior myocardial infarction
  90. Primary bacterial infectious disease
  91. Respiratory failure
  92. Respiratory system disease
  93. Skin disease
  94. Status asthmaticus
  95. Thyroid gland disease
  96. Tick paralysis
  97. Toxic myocarditis
  98. Trichinosis
  99. Tricuspid valve prolapse
  100. Urinary system disease
  101. Vascular disease
  102. Viral infectious disease

Stage Associations

This gene is associated with the following stages: