Gene Expression: SERPINC1

Gene Data

  • Gene Symbol: SERPINC1
  • Gene ID: 462
  • Synonyms: AT3, AT3D, ATIII, THPH7
  • Description: serpin peptidase inhibitor, clade C (antithrombin), member 1
  • Database Refs: HGNC:775, MIM:107300, Ensembl:ENSG00000117601, HPRD:00122, Vega:OTTHUMG00000037276
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 7 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 178 diseases, scroll to view all:
  1. Abdominal aortic aneurysm
  2. Acute myocardial infarction
  3. Acute pancreatitis
  4. Adult respiratory distress syndrome
  5. Alpha 1-antitrypsin deficiency
  6. Anemia
  7. Aneurysm
  8. Angioedema
  9. Antiphospholipid syndrome
  10. Antithrombin III deficiency
  11. Aortic aneurysm
  12. Aortic disease
  13. Arterial occlusive disease
  14. Arteriopathy
  15. Arteriosclerosis
  16. Arteriosclerotic cardiovascular disease
  17. Atherosclerosis
  18. Blood coagulation disease
  19. Blood platelet disease
  20. Blood protein disease
  21. Bone disease
  22. Bone marrow cancer
  23. Bone marrow disease
  24. Brain disease
  25. Brain infarction
  26. Cancer
  27. Carbohydrate metabolism disease
  28. Cardiovascular system disease
  29. Central nervous system disease
  30. Central retinal vein occlusion
  31. Cerebral infarction
  32. Cerebrovascular accident
  33. Cerebrovascular disease
  34. Congenital disorder of glycosylation
  35. Connective tissue disease
  36. Coronary arteriosclerosis
  37. Coronary heart disease
  38. Coronary thrombosis
  39. Cutaneous mastocytosis
  40. Diabetes mellitus
  41. Disease
  42. Disease by infectious agent
  43. Disease of anatomical entity
  44. Disease of cellular proliferation
  45. Disease of metabolism
  46. Disseminated intravascular coagulation
  47. Eclampsia
  48. Endocrine pancreas disease
  49. Endocrine system disease
  50. Extrinsic cardiomyopathy
  51. Eye and adnexa disease
  52. Eye disease
  53. Factor VII deficiency
  54. Female reproductive system disease
  55. Gastrointestinal system cancer
  56. Gastrointestinal system disease
  57. Genetic disease
  58. Giant hemangioma
  59. Globe disease
  60. Glucose metabolism disease
  61. Habitual abortion
  62. Heart disease
  63. Heart failure
  64. Heart septal defect
  65. Heart valve disease
  66. HELLP syndrome
  67. Hematologic cancer
  68. Hematopoietic system disease
  69. Hemiplegia
  70. Hemolytic anemia
  71. Hemophilia B
  72. Hemorrhagic disease
  73. Hepatic vascular disease
  74. Hepatic vein thrombosis
  75. Hepatitis
  76. Hepatobiliary disease
  77. Hepatocellular carcinoma
  78. Homocystinuria
  79. Hypercholesterolemia
  80. Hyperhomocysteinemia
  81. Hypersensitivity reaction disease
  82. Hypersensitivity reaction type II diseas
  83. Hypertension
  84. Immune system disease
  85. Inborn errors of amino acid metabolism
  86. Inborn errors of metabolism
  87. Inborn metabolic brain disease
  88. Inflammatory bowel disease
  89. Inherited blood coagulation disease
  90. Intermediate coronary syndrome
  91. Intermittent claudication
  92. Intestinal disease
  93. Intracranial embolism
  94. Intracranial sinus thrombosis
  95. Intracranial thrombosis
  96. Ischemia
  97. Ischemic bone disease
  98. Kidney disease
  99. Kidney failure
  100. Legg-Calve-Perthes Disease
  101. Leukemia
  102. Leukocyte disease
  103. Lipid metabolism disease
  104. Liver cancer
  105. Liver carcinoma
  106. Liver cirrhosis
  107. Liver disease
  108. Lower respiratory tract disease
  109. Lung disease
  110. Lupus erythematosus
  111. Lymphoblastic leukemia
  112. Mast cell neoplasm
  113. Metabolic brain disease
  114. Mild pre-eclampsia
  115. Mitral valve disease
  116. Mitral valve stenosis
  117. Monogenic disease
  118. Musculoskeletal system disease
  119. Myeloma
  120. Myocardial infarction
  121. Myocardial ischemia
  122. Nephritis
  123. Nephrosis
  124. Nephrotic syndrome
  125. Nervous system disease
  126. Newborn respiratory distress syndrome
  127. Normocytic anemia
  128. Organ system cancer
  129. Pancreas disease
  130. Pancreatitis
  131. Patent foramen ovale
  132. Peripheral vascular disease
  133. Peritonitis
  134. Phlebitis
  135. Placental abruption
  136. Placental infarction
  137. Placental necrosis
  138. Placental non-neoplastic disease
  139. Pneumonia
  140. Polycythemia
  141. Portal vein thrombosis
  142. Postphlebitic syndrome
  143. pre-eclampsia
  144. Pregnancy complication
  145. Pregnancy disease
  146. Protein C deficiency
  147. Protein S deficiency
  148. Proteinuria
  149. Pulmonary embolism
  150. Reproductive system disease
  151. Respiratory failure
  152. Respiratory system disease
  153. Retinal disease
  154. Retinal vascular disease
  155. Retinal vascular occlusion
  156. Retinal vein occlusion
  157. Rheumatic disease of mitral valve
  158. Sagittal sinus thrombosis
  159. Sensory system disease
  160. Severe pre-eclampsia
  161. Sneddon syndrome
  162. Spontaneous abortion
  163. Sulfuraminoacidemia
  164. Systemic lupus erythematosus
  165. Thrombocytopenia
  166. Thrombocytosis
  167. Thrombophilia
  168. Thrombophlebitis
  169. Thrombotic thrombocytopenic purpura
  170. Ulcerative colitis
  171. Urinary system disease
  172. Vascular disease
  173. Vascular skin disease
  174. Vasculitis
  175. Vein disease
  176. Venous insufficiency
  177. Viral infectious disease
  178. Vitamin K deficiency hemorrhagic disease

Stage Associations

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