History:GENE:ITGA3    GENE:PRAME    GENE:GAGE12I    

Gene Expression: THBD

Gene Data

  • Gene Symbol: THBD
  • Gene ID: 7056
  • Synonyms: AHUS6, BDCA3, CD141, THPH12, THRM, TM
  • Description: thrombomodulin
  • Database Refs: HGNC:11784, MIM:188040, Ensembl:ENSG00000178726, HPRD:01764, Vega:OTTHUMG00000032053
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 1 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters: No Clusters were found

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 108 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. Adenocarcinoma
  3. Adenomatoid tumor
  4. Adult respiratory distress syndrome
  5. Anemia
  6. Antiphospholipid syndrome
  7. Arterial occlusive disease
  8. Arteriopathy
  9. Arteriosclerosis
  10. Arteriosclerotic cardiovascular disease
  11. Atherosclerosis
  12. Benign mesothelioma
  13. Benign neoplasm
  14. Bladder adenocarcinoma
  15. Blood coagulation disease
  16. Blood platelet disease
  17. Brain disease
  18. Brain infarction
  19. Cancer
  20. Carbohydrate metabolism disease
  21. Carcinoma
  22. Cardiovascular system disease
  23. Carotid artery disease
  24. Cell type cancer
  25. Central nervous system disease
  26. Cerebral infarction
  27. Cerebrovascular accident
  28. Cerebrovascular disease
  29. Collagen disease
  30. Connective tissue disease
  31. Coronary heart disease
  32. Dengue disease
  33. Dengue hemorrhagic fever
  34. Dengue shock syndrome
  35. Diabetes mellitus
  36. Disease
  37. Disease by infectious agent
  38. Disease of anatomical entity
  39. Disease of cellular proliferation
  40. Disease of metabolism
  41. Disseminated intravascular coagulation
  42. Eclampsia
  43. Endocrine pancreas disease
  44. Endocrine system disease
  45. Essential hypertension
  46. Extrinsic cardiomyopathy
  47. Gastrointestinal system disease
  48. Glucose metabolism disease
  49. Heart disease
  50. Hematologic cancer
  51. Hematopoietic system disease
  52. Hemolytic anemia
  53. hemolytic-uremic syndrome
  54. Hemorrhagic disease
  55. Hepatobiliary disease
  56. Hypercholesterolemia
  57. Hyperhomocysteinemia
  58. Hypersensitivity reaction disease
  59. Hypersensitivity reaction type II diseas
  60. Hypertension
  61. Immune system disease
  62. Inborn errors of amino acid metabolism
  63. Inherited blood coagulation disease
  64. Intracranial thrombosis
  65. Ischemia
  66. Kidney disease
  67. Kidney failure
  68. Leukemia
  69. Liver disease
  70. Lower respiratory tract disease
  71. Lung disease
  72. Lupus erythematosus
  73. Malignant epithelial mesothelioma
  74. Malignant mesothelioma
  75. Malignant ovarian Brenner tumor
  76. Mesothelial neoplasm
  77. Mild pre-eclampsia
  78. Musculoskeletal system disease
  79. Myocardial infarction
  80. Myocardial ischemia
  81. Nephritis
  82. Nervous system disease
  83. Normocytic anemia
  84. Organ system cancer
  85. Pancreas disease
  86. Peripheral vascular disease
  87. Placental abruption
  88. pre-eclampsia
  89. Primary pulmonary hypertension
  90. Protein C deficiency
  91. Protein S deficiency
  92. Pulmonary embolism
  93. Pulmonary hypertension
  94. Respiratory failure
  95. Respiratory system disease
  96. Rheumatic disease
  97. Sarcomatoid mesothelioma
  98. Scleroderma
  99. Severe pre-eclampsia
  100. Systemic lupus erythematosus
  101. Systemic scleroderma
  102. Thrombocytopenia
  103. Thrombocytosis
  104. Thrombophilia
  105. Thrombotic thrombocytopenic purpura
  106. Urinary system disease
  107. Vascular disease
  108. Vasculitis

Stage Associations

This gene is associated with the following stages: No Stages were found