Gene Expression: APOB

Gene Data

  • Gene Symbol: APOB
  • Gene ID: 338
  • Synonyms: FLDB, LDLCQ4
  • Description: apolipoprotein B
  • Database Refs: HGNC:603, MIM:107730, Ensembl:ENSG00000084674, HPRD:00133, Vega:OTTHUMG00000090785
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 29 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 80 diseases, scroll to view all:
  1. Abetalipoproteinemia
  2. Acute myocardial infarction
  3. Aortic atherosclerosis
  4. Aortic disease
  5. Arcus senilis
  6. Arterial occlusive disease
  7. Arteriopathy
  8. Arteriosclerosis
  9. Arteriosclerotic cardiovascular disease
  10. Atherosclerosis
  11. Brain disease
  12. Brain infarction
  13. Carbohydrate metabolism disease
  14. Cardiovascular system disease
  15. Carotid artery disease
  16. Central nervous system disease
  17. Cerebrovascular accident
  18. Cerebrovascular disease
  19. Chronic kidney failure
  20. Coronary heart disease
  21. Coronary stenosis
  22. Diabetes mellitus
  23. Diabetes mellitus type 1
  24. Diabetes mellitus type 2
  25. Disease
  26. Disease of anatomical entity
  27. Disease of metabolism
  28. End stage renal failure
  29. Endocrine pancreas disease
  30. Endocrine system disease
  31. Essential hypertension
  32. Extrinsic cardiomyopathy
  33. Familial combined hyperlipidemia
  34. Familial hypercholesterolemia
  35. Familial hyperlipidemia
  36. Familial hyperlipoproteinemia
  37. Familial hypertriglyceridemia
  38. Familial lipoprotein lipase deficiency
  39. Fatty liver
  40. Gastrointestinal system disease
  41. Genetic disorder
  42. Glucose intolerance
  43. Glucose metabolism disease
  44. Heart disease
  45. Hepatobiliary disease
  46. Hypercholesterolemia
  47. Hyperglycemia
  48. Hyperhomocysteinemia
  49. Hyperinsulinism
  50. Hypertension
  51. Hyperuricemia
  52. Hypobetalipoproteinemia
  53. Hypolipoproteinemia
  54. Hypothyroidism
  55. Inborn errors lipid metabolism
  56. Inborn errors of amino acid metabolism
  57. Intermediate coronary syndrome
  58. Ischemia
  59. Kidney disease
  60. Kidney failure
  61. Lipid metabolism disease
  62. Lipodystrophy
  63. Liver disease
  64. Medical disorder
  65. Musculoskeletal system disease
  66. Myocardial infarction
  67. Myocardial ischemia
  68. Nephrosis
  69. Nephrotic syndrome
  70. Nervous system disease
  71. Norum disease
  72. Pancreas disease
  73. Proteinuria
  74. Steatorrhea
  75. Tangier disease
  76. Thyroid gland disease
  77. Uremia
  78. Urinary system disease
  79. Vascular disease
  80. Xanthomatosis

Stage Associations

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