History:GENE:MEF2A    

Gene Expression: TNNT2

Gene Data

  • Gene Symbol: TNNT2
  • Gene ID: 7139
  • Synonyms: CMH2, CMPD2, LVNC6, RCM3, TnTC, cTnT
  • Description: troponin T type 2 (cardiac)
  • Database Refs: HGNC:11949, MIM:191045, Ensembl:ENSG00000118194, HPRD:01844, Vega:OTTHUMG00000035733
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 4 out of 28 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 74 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. Acute myocarditis
  3. Amyloidosis
  4. Anterolateral myocardial infarction
  5. Aortic valve stenosis
  6. Arterial occlusive disease
  7. Arteriopathy
  8. Arteriosclerosis
  9. Arteriosclerotic cardiovascular disease
  10. Atherosclerosis
  11. Brain disease
  12. Carbohydrate metabolism disease
  13. Cardiac sarcoidosis
  14. Cardiovascular system disease
  15. Central nervous system disease
  16. Cerebrovascular accident
  17. Cerebrovascular disease
  18. Chronic kidney failure
  19. Commensal bacterial infectious disease
  20. Conduction disease
  21. Congenital heart defect
  22. Congenital structural myopathy
  23. Congestive heart failure
  24. Coronary arteriosclerosis
  25. Coronary artery vasospasm
  26. Coronary heart disease
  27. Coronary stenosis
  28. Diabetes mellitus
  29. Dilated cardiomyopathy
  30. Disease
  31. Disease of anatomical entity
  32. Disease of metabolism
  33. End stage renal failure
  34. Endocrine pancreas disease
  35. Endocrine system disease
  36. Extrinsic cardiomyopathy
  37. Familial hypertrophic cardiomyopathy
  38. Gas gangrene
  39. Gastrointestinal system disease
  40. Genetic disease
  41. Glucose metabolism disease
  42. Heart disease
  43. Heart failure
  44. Heart valve disease
  45. Hypertension
  46. Hypertrophic cardiomyopathy
  47. Intermediate coronary syndrome
  48. Intrinsic cardiomyopathy
  49. Ischemia
  50. Kidney disease
  51. Kidney failure
  52. Medical disorder
  53. Mitral valve insufficiency
  54. Monogenic disease
  55. Muscle tissue disease
  56. Muscular disease
  57. Musculoskeletal system disease
  58. Myocardial infarction
  59. Myocardial ischemia
  60. Myocardial stunning
  61. Myocarditis
  62. Myopathy
  63. Myositis
  64. Myotonic disease
  65. Myotonic dystrophy
  66. Nemaline myopathy
  67. Nervous system disease
  68. Pancreas disease
  69. Physical disorder
  70. Pulmonary embolism
  71. Restrictive cardiomyopathy
  72. Urinary system disease
  73. Vascular disease
  74. Ventricular septal defect

Stage Associations

This gene is associated with the following stages: