Gene Expression: F12

Gene Data

  • Gene Symbol: F12
  • Gene ID: 2161
  • Synonyms: HAE3, HAEX, HAF
  • Description: coagulation factor XII (Hageman factor)
  • Database Refs: HGNC:3530, MIM:610619, Ensembl:ENSG00000131187, HPRD:01992, Vega:OTTHUMG00000163403
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 14 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 69 diseases, scroll to view all:
  1. Acalculous cholecystitis
  2. Acute myocardial infarction
  3. Angioedema
  4. Antiphospholipid syndrome
  5. Arteriopathy
  6. Articular gout (disorder)
  7. Atrial heart septal defect
  8. Blood coagulation disease
  9. Blood platelet disease
  10. Brain disease
  11. C1 inhibitor deficiency
  12. Cardiovascular system disease
  13. Central nervous system disease
  14. Cerebrovascular accident
  15. Cerebrovascular disease
  16. Complement deficiency
  17. Connective tissue disease
  18. Coronary heart disease
  19. Dermatitis
  20. Disease
  21. Disease by infectious agent
  22. Disease of anatomical entity
  23. Disseminated intravascular coagulation
  24. Extrinsic cardiomyopathy
  25. Factor VII deficiency
  26. Factor VIII deficiency
  27. Factor XI deficiency
  28. Factor XII deficiency
  29. Gastrointestinal system disease
  30. Genetic disease
  31. Habitual abortion
  32. Heart disease
  33. Hematopoietic system disease
  34. Hemophilia B
  35. Hemorrhagic disease
  36. Hepatobiliary disease
  37. Hereditary angioedema
  38. Hypersensitivity reaction disease
  39. Hypersensitivity reaction type II diseas
  40. Immune system disease
  41. Inherited blood coagulation disease
  42. Integumentary system disease
  43. Ischemia
  44. Kidney disease
  45. Liver disease
  46. Lupus erythematosus
  47. Monogenic disease
  48. Myocardial infarction
  49. Myocardial ischemia
  50. Necrotizing fasciitis
  51. Nephritis
  52. Nephrosis
  53. Nephrotic syndrome
  54. Nervous system disease
  55. Patent foramen ovale
  56. Peripheral vascular disease
  57. Pregnancy complication
  58. Pregnancy disease
  59. Protein C deficiency
  60. Protein S deficiency
  61. Skin disease
  62. Spontaneous abortion
  63. Thrombocytopenia
  64. Thrombophilia
  65. Urinary system disease
  66. Urticaria
  67. Vascular disease
  68. Vascular skin disease
  69. Von Willebrand's disease

Stage Associations

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