Gene Expression: CP

Gene Data

  • Gene Symbol: CP
  • Gene ID: 1356
  • Synonyms: CP-2
  • Description: ceruloplasmin (ferroxidase)
  • Database Refs: HGNC:2295, MIM:117700, Ensembl:ENSG00000047457, HPRD:00317, Vega:OTTHUMG00000159563
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 18 out of 26 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 119 diseases, scroll to view all:
  1. Age related macular degeneration
  2. Agranulocytosis
  3. Allergic urticaria
  4. Alzheimer's disease
  5. Anemia
  6. Anthracosilicosis
  7. Arterial occlusive disease
  8. Arteriopathy
  9. Arteriosclerosis
  10. Arteriosclerotic cardiovascular disease
  11. Arthritis
  12. Atherosclerosis
  13. Autoimmune disease of urogenital tract
  14. Bacterial infectious disease
  15. Basal ganglia disease
  16. Bile duct disease
  17. Biliary tract disease
  18. Bone disease
  19. Bone inflammation disease
  20. Brain disease
  21. Cancer
  22. Carbohydrate metabolism disease
  23. Cardiovascular system disease
  24. Central nervous system disease
  25. Cholestasis
  26. Cognitive disease
  27. Degeneration of macula and posterior pol
  28. Dementia
  29. Diabetes mellitus
  30. Diaper rash
  31. Disease
  32. Disease by infectious agent
  33. Disease of anatomical entity
  34. Disease of cellular proliferation
  35. Disease of mental health
  36. Disease of metabolism
  37. Endocrine pancreas disease
  38. Endocrine system disease
  39. Extrinsic cardiomyopathy
  40. Eye and adnexa disease
  41. Eye disease
  42. Gastrointestinal system cancer
  43. Gastrointestinal system disease
  44. Globe disease
  45. Glucose metabolism disease
  46. Hair disease
  47. Hallervorden-Spatz syndrome
  48. Heart disease
  49. Hematopoietic system disease
  50. Hemochromatosis
  51. Hemolytic anemia
  52. Hemosiderosis
  53. Hepatitis
  54. Hepatobiliary disease
  55. Hepatocellular carcinoma
  56. Hypersensitivity reaction disease
  57. Hypersensitivity reaction type II diseas
  58. Hypertension
  59. Hypochromic anemia
  60. Immune system disease
  61. Inborn errors metal metabolism
  62. Inborn errors of metabolism
  63. Integumentary system disease
  64. Interstitial lung disease
  65. Iron deficiency anemia
  66. Iron metabolism disease
  67. Ischemia
  68. Kidney disease
  69. Leukocyte disease
  70. Leukopenia
  71. Liver cancer
  72. Liver carcinoma
  73. Liver cirrhosis
  74. Liver disease
  75. Lower respiratory tract disease
  76. Lung disease
  77. Macular degeneration
  78. Malignant choroid melanoma
  79. Menkes disease
  80. Microcytic anemia
  81. Mineral metabolism disease
  82. Musculoskeletal system disease
  83. Myocardial infarction
  84. Myocardial ischemia
  85. Nervous system disease
  86. Neurodegenerative disease
  87. Neutropenia
  88. Normocytic anemia
  89. Nutmeg liver
  90. Nutrition disease
  91. Nutritional deficiency disease
  92. Organ system cancer
  93. Pancreas disease
  94. Parkinson's disease
  95. Pneumoconiosis
  96. pre-eclampsia
  97. Primary bacterial infectious disease
  98. Primary biliary cirrhosis
  99. Protoplasmic astrocytoma
  100. Psoriasis
  101. Psychotic disease
  102. Pulmonary tuberculosis
  103. Respiratory system disease
  104. Retinal degeneration
  105. Retinal disease
  106. Rheumatoid arthritis
  107. Schizophrenia
  108. Scurvy
  109. Sensory system disease
  110. Skeletal tuberculosis
  111. Skin disease
  112. Swayback
  113. Tauopathy
  114. Tuberculosis
  115. Ulcerative blepharitis
  116. Urinary system disease
  117. Vascular disease
  118. Viral hepatitis
  119. Wilson disease

Stage Associations

This gene is associated with the following stages: