Gene Expression: F5

Gene Data

  • Gene Symbol: F5
  • Gene ID: 2153
  • Synonyms: FVL, PCCF, RPRGL1, THPH2
  • Description: coagulation factor V (proaccelerin, labile factor)
  • Database Refs: HGNC:3542, MIM:612309, HPRD:01964
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 26 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 160 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. Antiphospholipid syndrome
  3. Antithrombin III deficiency
  4. Arterial occlusive disease
  5. Arteriopathy
  6. Arteriosclerosis
  7. Arteriosclerotic cardiovascular disease
  8. Atherosclerosis
  9. Atrial heart septal defect
  10. Blood coagulation disease
  11. Blood platelet disease
  12. Blood protein disease
  13. Bone marrow cancer
  14. Bone marrow disease
  15. Brain disease
  16. Brain hypoxia-Ischemia
  17. Brain infarction
  18. Brain ischemia
  19. Branch retinal artery occlusion
  20. Cancer
  21. Carbohydrate metabolism disease
  22. Cardiovascular system disease
  23. Central nervous system disease
  24. Central retinal artery occlusion
  25. Central retinal vein occlusion
  26. Cerebral infarction
  27. Cerebral palsy
  28. Cerebrovascular accident
  29. Cerebrovascular disease
  30. Chickenpox
  31. Congenital heart defect
  32. Connective tissue disease
  33. Coronary arteriosclerosis
  34. Coronary heart disease
  35. Coronary thrombosis
  36. Crohn's disease
  37. Diabetes mellitus
  38. Disease
  39. Disease of anatomical entity
  40. Disease of cellular proliferation
  41. Disease of metabolism
  42. Disseminated intravascular coagulation
  43. Eclampsia
  44. Endocrine pancreas disease
  45. Endocrine system disease
  46. Extrinsic cardiomyopathy
  47. Eye and adnexa disease
  48. Eye disease
  49. Factor V deficiency
  50. Factor VII deficiency
  51. Factor VIII deficiency
  52. Factor XI deficiency
  53. Factor XIII deficiency
  54. Female reproductive system disease
  55. Gastrointestinal system disease
  56. Genetic disease
  57. Globe disease
  58. Glucose metabolism disease
  59. Habitual abortion
  60. Heart disease
  61. Heart septal defect
  62. HELLP syndrome
  63. Hematologic cancer
  64. Hematopoietic system disease
  65. Hemiplegia
  66. Hemorrhagic disease
  67. Hepatic vascular disease
  68. Hepatic vein thrombosis
  69. Hepatitis
  70. Hepatobiliary disease
  71. Homocystinuria
  72. Hyperhomocysteinemia
  73. Hypersensitivity reaction disease
  74. Hypersensitivity reaction type II diseas
  75. Hypertension
  76. Immune system disease
  77. Inborn errors of amino acid metabolism
  78. Inborn errors of metabolism
  79. Inborn metabolic brain disease
  80. Inflammatory bowel disease
  81. Inherited blood coagulation disease
  82. Intestinal disease
  83. Intracranial hypertension
  84. Intracranial sinus thrombosis
  85. Intracranial thrombosis
  86. Ischemia
  87. Ischemic bone disease
  88. Ischemic optic neuropathy
  89. Kidney disease
  90. Lateral sinus thrombosis
  91. Legg-Calve-Perthes Disease
  92. Liver cirrhosis
  93. Liver disease
  94. Lupus erythematosus
  95. Medical disorder
  96. Metabolic brain disease
  97. Migraine
  98. Monogenic disease
  99. Musculoskeletal system disease
  100. Myocardial infarction
  101. Myocardial ischemia
  102. Nephrosis
  103. Nervous system disease
  104. Optic nerve disease
  105. Organ system cancer
  106. Osteonecrosis
  107. Ovarian hyperstimulation syndrome
  108. Pancreas disease
  109. Patent foramen ovale
  110. Peripheral vascular disease
  111. Phlebitis
  112. Physical disorder
  113. Placenta disease
  114. Placental abruption
  115. Placental infarction
  116. Placental necrosis
  117. Placental non-neoplastic disease
  118. Polycythemia
  119. Polycythemia vera
  120. Portal hypertension
  121. Portal vein thrombosis
  122. Postphlebitic syndrome
  123. pre-eclampsia
  124. Pregnancy complication
  125. Pregnancy disease
  126. Protein C deficiency
  127. Protein S deficiency
  128. Pseudotumor cerebri
  129. Pulmonary embolism
  130. Reproductive system disease
  131. Retinal artery occlusion
  132. Retinal disease
  133. Retinal vascular disease
  134. Retinal vascular occlusion
  135. Retinal vein occlusion
  136. Sagittal sinus thrombosis
  137. Sensory system disease
  138. Severe pre-eclampsia
  139. Sickle cell anemia
  140. Sneddon syndrome
  141. Spastic cerebral palsy
  142. Spastic hemiplegia
  143. Spontaneous abortion
  144. Sulfuraminoacidemia
  145. Systemic lupus erythematosus
  146. Thrombocytopenia
  147. Thrombocytosis
  148. Thrombophilia
  149. Thrombophlebitis
  150. Thrombotic thrombocytopenic purpura
  151. Transient cerebral ischemia
  152. Ulcerative colitis
  153. Urinary system disease
  154. Uterine disease
  155. Vascular disease
  156. Vasculitis
  157. Vein disease
  158. Venous insufficiency
  159. Visual pathway disease
  160. Vitamin K deficiency hemorrhagic disease

Stage Associations

This gene is associated with the following stages: