Gene Expression: PPBP

Gene Data

  • Gene Symbol: PPBP
  • Gene ID: 5473
  • Synonyms: B-TG1, Beta-TG, CTAP-III, CTAP3, CTAPIII, CXCL7, LA-PF4, LDGF, MDGF, NAP-2, PBP, SCYB7, TC1, TC2, TGB, TGB1, THBGB, THBGB1
  • Description: pro-platelet basic protein (chemokine (C-X-C motif) ligand 7)
  • Database Refs: HGNC:9240, MIM:121010, HPRD:07171
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 3 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 99 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. Arterial occlusive disease
  3. Arteriopathy
  4. Arteriosclerosis
  5. Arteriosclerotic cardiovascular disease
  6. Atherosclerosis
  7. Autoimmune disease of blood
  8. Autoimmune thrombocytopenic purpura
  9. Blood coagulation disease
  10. Blood platelet disease
  11. Bone marrow cancer
  12. Bone marrow disease
  13. Brain disease
  14. Brain hypoxia-Ischemia
  15. Brain infarction
  16. Brain ischemia
  17. Cancer
  18. Carbohydrate metabolism disease
  19. Cardiovascular system disease
  20. Central nervous system disease
  21. Cerebral infarction
  22. Cerebrovascular accident
  23. Cerebrovascular disease
  24. Chronic myeloproliferative disease
  25. Classic migraine
  26. Collagen disease
  27. Colloid adenoma
  28. Common migraine
  29. Connective tissue disease
  30. Coronary arteriosclerosis
  31. Coronary artery vasospasm
  32. Coronary heart disease
  33. Diabetes mellitus
  34. Diabetic angiopathy
  35. Disease
  36. Disease of anatomical entity
  37. Disease of cellular proliferation
  38. Disease of metabolism
  39. Disseminated intravascular coagulation
  40. Endocrine pancreas disease
  41. Endocrine system disease
  42. Erythromelalgia
  43. Essential hypertension
  44. Extrinsic cardiomyopathy
  45. Gastrointestinal system disease
  46. Glucose metabolism disease
  47. Heart aneurysm
  48. Heart disease
  49. Heart valve disease
  50. Heart valve prolapse
  51. Hematologic cancer
  52. Hematopoietic system disease
  53. Hemorrhagic disease
  54. Hemorrhagic thrombocythemia
  55. Hypersensitivity reaction disease
  56. Hypersensitivity reaction type II diseas
  57. Hypertension
  58. Immune system disease
  59. Intermediate coronary syndrome
  60. Intermittent claudication
  61. Ischemia
  62. Kidney disease
  63. Kidney failure
  64. Leukemia
  65. Lower respiratory tract disease
  66. Lung disease
  67. Megakaryocytic leukemia
  68. Migraine
  69. Mitral valve disease
  70. Mitral valve prolapse
  71. Mitral valve stenosis
  72. Musculoskeletal system disease
  73. Myelofibrosis
  74. Myeloma
  75. Myocardial infarction
  76. Myocardial ischemia
  77. Nervous system disease
  78. Obstructive lung disease
  79. Organ system cancer
  80. Pancreas disease
  81. Peripheral vascular disease
  82. Platelet storage pool deficiency
  83. Polycythemia
  84. Polycythemia vera
  85. pre-eclampsia
  86. Primary thrombocytopenia
  87. Pulmonary embolism
  88. Respiratory system disease
  89. Rheumatic disease
  90. Rheumatic disease of mitral valve
  91. Scleroderma
  92. Severe pre-eclampsia
  93. Systemic scleroderma
  94. Thrombocytopenia
  95. Thrombocytosis
  96. Thrombophilia
  97. Transient cerebral ischemia
  98. Urinary system disease
  99. Vascular disease

Stage Associations

This gene is associated with the following stages: