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Gene Expression: F7

Gene Data

  • Gene Symbol: F7
  • Gene ID: 2155
  • Synonyms: SPCA
  • Description: coagulation factor VII (serum prothrombin conversion accelerator)
  • Database Refs: HGNC:3544, MIM:613878, Ensembl:ENSG00000057593, HPRD:01965, Vega:OTTHUMG00000017373
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 10 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 86 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. Angiodysplasia
  3. Arterial occlusive disease
  4. Arteriopathy
  5. Arteriosclerosis
  6. Arteriosclerotic cardiovascular disease
  7. Arthropathy
  8. Atherosclerosis
  9. Bernard-Soulier syndrome
  10. Blood coagulation disease
  11. Blood platelet disease
  12. Brain disease
  13. Brain infarction
  14. Cancer
  15. Carbohydrate metabolism disease
  16. Cardiovascular system disease
  17. Carotid artery disease
  18. Central nervous system disease
  19. Cerebral infarction
  20. Cerebrovascular accident
  21. Cerebrovascular disease
  22. Compartment syndrome
  23. Coronary arteriosclerosis
  24. Coronary heart disease
  25. Coronary thrombosis
  26. Diabetes mellitus
  27. Diabetes mellitus type 2
  28. Disease
  29. Disease of anatomical entity
  30. Disease of cellular proliferation
  31. Disease of metabolism
  32. Disseminated intravascular coagulation
  33. Endocrine pancreas disease
  34. Endocrine system disease
  35. Extrinsic cardiomyopathy
  36. Factor V deficiency
  37. Factor VII deficiency
  38. Factor VIII deficiency
  39. Factor X deficiency
  40. Factor XI deficiency
  41. Familial hyperlipidemia
  42. Gastrointestinal system disease
  43. Genetic disease
  44. Glanzmann's thrombasthenia
  45. Glucose metabolism disease
  46. Heart disease
  47. Hemarthrosis
  48. Hematopoietic system disease
  49. Hemophilia B
  50. Hemorrhagic disease
  51. Hepatic vascular disease
  52. Hepatobiliary disease
  53. Hypercholesterolemia
  54. Hypertension
  55. Inborn errors lipid metabolism
  56. Inherited blood coagulation disease
  57. Intermediate coronary syndrome
  58. Intracranial thrombosis
  59. Ischemia
  60. Kidney disease
  61. Lipid metabolism disease
  62. Liver cirrhosis
  63. Liver disease
  64. Monogenic disease
  65. Myocardial infarction
  66. Myocardial ischemia
  67. Nervous system disease
  68. Nutrition disease
  69. Nutritional deficiency disease
  70. Organ system cancer
  71. Pancreas disease
  72. Peripheral vascular disease
  73. Phlebitis
  74. Placenta accreta
  75. Protein C deficiency
  76. Pulmonary embolism
  77. Respiratory failure
  78. Thrombocytopenia
  79. Thrombophilia
  80. Thrombophlebitis
  81. Urinary system disease
  82. Uterine Inversion
  83. Vascular disease
  84. Vein disease
  85. Vitamin K deficiency hemorrhagic disease
  86. Von Willebrand's disease

Stage Associations

This gene is associated with the following stages: