Gene Expression: PROS1

Gene Data

  • Gene Symbol: PROS1
  • Gene ID: 5627
  • Synonyms: PROS, PS21, PS22, PS23, PS24, PS25, PSA, THPH5, THPH6
  • Description: protein S (alpha)
  • Database Refs: HGNC:9456, MIM:176880, Ensembl:ENSG00000184500, HPRD:01473, Vega:OTTHUMG00000150354
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 17 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 125 diseases, scroll to view all:
  1. Antiphospholipid syndrome
  2. Antithrombin III deficiency
  3. Aphasia
  4. Arterial occlusive disease
  5. Arteriopathy
  6. Arteriosclerosis
  7. Arteriosclerotic cardiovascular disease
  8. Atherosclerosis
  9. Beta thalassemia
  10. Blood coagulation disease
  11. Blood platelet disease
  12. Blood protein disease
  13. Blue toe syndrome
  14. Bone marrow cancer
  15. Bone marrow disease
  16. Brain disease
  17. Brain infarction
  18. Branch retinal artery occlusion
  19. Cancer
  20. Cardiovascular system disease
  21. Cavernous sinus thrombosis
  22. Cell type cancer
  23. Central nervous system disease
  24. Central retinal vein occlusion
  25. Cerebral infarction
  26. Cerebrovascular accident
  27. Cerebrovascular disease
  28. Chickenpox
  29. Cholesterol embolism
  30. Communication disease
  31. Connective tissue disease
  32. Disease
  33. Disease by infectious agent
  34. Disease of anatomical entity
  35. Disease of cellular proliferation
  36. Disease of metabolism
  37. Disseminated intravascular coagulation
  38. Endocrine system disease
  39. Extrinsic cardiomyopathy
  40. Factor XII deficiency
  41. Female reproductive system disease
  42. Gastrointestinal system disease
  43. Genetic disease
  44. Habitual abortion
  45. Heart disease
  46. Hematologic cancer
  47. Hematopoietic system disease
  48. Hemophilia B
  49. Hemorrhagic disease
  50. Hepatic vascular disease
  51. Hepatic vein thrombosis
  52. Hepatobiliary disease
  53. Homocystinuria
  54. Hyperhomocysteinemia
  55. Hypersensitivity reaction disease
  56. Hypersensitivity reaction type II diseas
  57. Hypertension
  58. Immune system disease
  59. Inborn errors of amino acid metabolism
  60. Inborn errors of metabolism
  61. Inflammatory bowel disease
  62. Inherited blood coagulation disease
  63. Intestinal disease
  64. Intracranial sinus thrombosis
  65. Intracranial thrombosis
  66. Ischemia
  67. Ischemic bone disease
  68. Ischemic optic neuropathy
  69. Kidney disease
  70. Language disease
  71. Legg-Calve-Perthes Disease
  72. Liver cirrhosis
  73. Liver disease
  74. Lupus erythematosus
  75. Monogenic disease
  76. Musculoskeletal system disease
  77. Myeloma
  78. Myocardial infarction
  79. Myocardial ischemia
  80. Nephrosis
  81. Nephrotic syndrome
  82. Nervous system disease
  83. Nutrition disease
  84. Nutritional deficiency disease
  85. Organ system cancer
  86. Osteonecrosis
  87. Partial motor epilepsy
  88. Patent foramen ovale
  89. Phlebitis
  90. Placental abruption
  91. Placental infarction
  92. Placental necrosis
  93. Polycythemia
  94. Portal hypertension
  95. Portal vein thrombosis
  96. pre-eclampsia
  97. Pregnancy complication
  98. Pregnancy disease
  99. Protein C deficiency
  100. Protein S deficiency
  101. Pulmonary embolism
  102. Reproductive system disease
  103. Retinal artery occlusion
  104. Retinal vascular disease
  105. Retinal vascular occlusion
  106. Retinal vein occlusion
  107. Sagittal sinus thrombosis
  108. Sensory system disease
  109. Severe pre-eclampsia
  110. Sneddon syndrome
  111. Splenic infarction
  112. Spontaneous abortion
  113. Sulfuraminoacidemia
  114. Systemic lupus erythematosus
  115. Thalassemia
  116. Thrombocytopenia
  117. Thrombocytosis
  118. Thrombophilia
  119. Thrombophlebitis
  120. Urinary system disease
  121. Vascular disease
  122. Vasculitis
  123. Vein disease
  124. Viral infectious disease
  125. Vitamin K deficiency hemorrhagic disease

Stage Associations

This gene is associated with the following stages: