Gene Expression: VWF

Gene Data

  • Gene Symbol: VWF
  • Gene ID: 7450
  • Synonyms: F8VWF, VWD
  • Description: von Willebrand factor
  • Database Refs: HGNC:12726, MIM:613160, Ensembl:ENSG00000110799, HPRD:01906, Vega:OTTHUMG00000168265
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 56 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 170 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. Anemia
  3. Angiodysplasia
  4. Angiosarcoma
  5. Antiphospholipid syndrome
  6. Aortic valve disease
  7. Aortic valve stenosis
  8. Arterial occlusive disease
  9. Arteriopathy
  10. Arteriosclerosis
  11. Arteriosclerotic cardiovascular disease
  12. Arthritis
  13. Arthropathy
  14. Atherosclerosis
  15. Autoimmune disease of blood
  16. Autoimmune thrombocytopenic purpura
  17. Bernard-Soulier syndrome
  18. Blood coagulation disease
  19. Blood platelet disease
  20. Bone disease
  21. Bone inflammation disease
  22. Bone marrow cancer
  23. Bone marrow disease
  24. Brain disease
  25. Brain infarction
  26. Cancer
  27. Capillary hemangioma
  28. Carbohydrate metabolism disease
  29. Carcinoma
  30. Cardiovascular cancer
  31. Cardiovascular system disease
  32. Carotid artery disease
  33. Cell type cancer
  34. Central nervous system disease
  35. Central nervous system vasculitis
  36. Cerebral infarction
  37. Cerebrovascular accident
  38. Cerebrovascular disease
  39. Childhood type dermatomyositis
  40. Chronic kidney failure
  41. Chronic myeloproliferative disease
  42. Chronic pulmonary heart disease
  43. Collagen disease
  44. Congenital afibrinogenemia
  45. Connective tissue disease
  46. Cor pulmonale
  47. Coronary arteriosclerosis
  48. Coronary heart disease
  49. Coronary thrombosis
  50. Dermatomyositis
  51. Diabetes mellitus
  52. Diabetes mellitus type 2
  53. Diabetic angiopathy
  54. Diabetic retinopathy
  55. Disease
  56. Disease by infectious agent
  57. Disease of anatomical entity
  58. Disease of cellular proliferation
  59. Disease of metabolism
  60. Disseminated intravascular coagulation
  61. End stage renal failure
  62. Endocrine pancreas disease
  63. Endocrine system disease
  64. Erythromelalgia
  65. Essential hypertension
  66. Extrinsic cardiomyopathy
  67. Eye and adnexa disease
  68. Eye disease
  69. Factor VIII deficiency
  70. Factor XI deficiency
  71. Factor XII deficiency
  72. Factor XIII deficiency
  73. Familial hyperlipidemia
  74. Gastrointestinal system disease
  75. Genetic disease
  76. Glanzmann's thrombasthenia
  77. Globe disease
  78. Glucose metabolism disease
  79. Heart disease
  80. Heart failure
  81. Heart valve disease
  82. Hemangioma
  83. Hemarthrosis
  84. Hematologic cancer
  85. Hematopoietic system disease
  86. Hemolytic anemia
  87. hemolytic-uremic syndrome
  88. Hemophilia B
  89. Hemorrhagic disease
  90. Hemorrhagic thrombocythemia
  91. Hepatic vascular disease
  92. Hepatobiliary disease
  93. Hypercholesterolemia
  94. Hyperhomocysteinemia
  95. Hypersensitivity reaction disease
  96. Hypersensitivity reaction type II diseas
  97. Hypertension
  98. Hypothyroidism
  99. Immune system disease
  100. Inborn errors of amino acid metabolism
  101. Inborn errors of metabolism
  102. Infiltrating angiolipoma
  103. Inherited blood coagulation disease
  104. Integumentary system disease
  105. Intermediate coronary syndrome
  106. Intermittent claudication
  107. Intracranial thrombosis
  108. Ischemia
  109. Kidney disease
  110. Kidney failure
  111. Leukemia
  112. Lipid metabolism disease
  113. Liver cirrhosis
  114. Liver disease
  115. Lower respiratory tract disease
  116. Lung disease
  117. Lupus erythematosus
  118. Malignant vascular tumor
  119. Mitral valve disease
  120. Mitral valve stenosis
  121. Monogenic disease
  122. Multiple myeloma
  123. Musculoskeletal system disease
  124. Myelofibrosis
  125. Myeloma
  126. Myocardial infarction
  127. Myocardial ischemia
  128. Nephritis
  129. Nervous system disease
  130. Normocytic anemia
  131. Organ system cancer
  132. Pancreas disease
  133. Peripheral vascular disease
  134. Polycythemia
  135. Polycythemia vera
  136. Polymyalgia rheumatica
  137. pre-eclampsia
  138. Primary pulmonary hypertension
  139. Primary thrombocytopenia
  140. Proliferative diabetic retinopathy
  141. Proteinuria
  142. Pulmonary hypertension
  143. Reproductive system disease
  144. Respiratory failure
  145. Respiratory system disease
  146. Retinal disease
  147. Retinal vascular disease
  148. Rheumatic disease
  149. Rheumatic disease of mitral valve
  150. Rheumatoid arthritis
  151. Scleroderma
  152. Sensory system disease
  153. Severe pre-eclampsia
  154. Skin disease
  155. Systemic lupus erythematosus
  156. Systemic scleroderma
  157. Temporal arteritis
  158. Thrombocytopenia
  159. Thrombocytosis
  160. Thrombophilia
  161. Thrombotic thrombocytopenic purpura
  162. Thyroid gland disease
  163. Uremia
  164. Urinary system disease
  165. Vascular disease
  166. Vascular tissue disease
  167. Vasculitis
  168. Vein disease
  169. Viral infectious disease
  170. Von Willebrand's disease

Stage Associations

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