History:GENE:NGF    GENE:TAC1    

Gene Expression: NCOA1

Gene Data

  • Gene Symbol: NCOA1
  • Gene ID: 8648
  • Synonyms: F-SRC-1, KAT13A, RIP160, SRC1, bHLHe42, bHLHe74
  • Description: nuclear receptor coactivator 1
  • Database Refs: HGNC:7668, MIM:602691, Ensembl:ENSG00000084676, HPRD:04070, Vega:OTTHUMG00000125523
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 24 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 88 diseases, scroll to view all:
  1. Aneurysm
  2. Ankylosis
  3. Aortic aneurysm
  4. Aortic disease
  5. Arteriovenous malformation
  6. Arthropathy
  7. Bone development disease
  8. Bone disease
  9. Bone inflammation disease
  10. Bone structure disease
  11. Brain disease
  12. Brain infarction
  13. Brain stem infarction
  14. Breast cancer
  15. Calcaneonavicular coalition
  16. Cancer
  17. Cardiovascular system disease
  18. Carotid artery dissection
  19. Carotid stenosis
  20. Cell type cancer
  21. Central nervous system disease
  22. Cerebral palsy
  23. Cerebrovascular disease
  24. Cholecystolithiasis
  25. Chronic maxillary sinusitis
  26. Cleft lip
  27. Cranial nerve disease
  28. Craniosynostosis
  29. Crouzon syndrome
  30. Disease
  31. Disease of anatomical entity
  32. Disease of cellular proliferation
  33. Double outlet right ventricle
  34. Dysostosis
  35. Enophthalmos
  36. Enterocele
  37. External ear cancer
  38. External ear carcinoma
  39. Facial hemiatrophy
  40. Facial nerve disease
  41. Facial neuralgia
  42. Gastrointestinal system cancer
  43. Goldenhar syndrome
  44. Hemangioma
  45. Hilar cholangiocellular carcinoma
  46. Hyperlucent lung
  47. Intracranial aneurysm
  48. Intracranial hypotension
  49. Jaw cancer
  50. Klippel-Feil syndrome
  51. Lung cancer
  52. Maxillary neoplasm
  53. Maxillary sinusitis
  54. Medical disorder
  55. Meningocele
  56. Moyamoya disease
  57. Musculoskeletal system disease
  58. Nervous system disease
  59. Neurilemmoma
  60. Neuroma
  61. Organ system cancer
  62. Orofacial cleft
  63. Physical disorder
  64. Prolapse of female genital organ
  65. Respiratory system cancer
  66. Spastic diplegia
  67. Spastic quadriplegia
  68. Spina bifida
  69. Spinal cord disease
  70. Spondylolisthesis
  71. Spondylolysis
  72. Superior mesenteric artery syndrome
  73. Synostosis
  74. Tethered spinal cord syndrome
  75. Thoracic cancer
  76. Thoracic outlet syndrome
  77. Tracheal disease
  78. Tracheal neoplasm
  79. Tracheal stenosis
  80. Trigeminal nerve disease
  81. Trigeminal neuralgia
  82. Ureteral neoplasm
  83. Vascular disease
  84. Vascular tissue disease
  85. Vertebral artery insufficiency
  86. Vertebral artery occlusion
  87. Vertebrobasilar insufficiency
  88. Xanthogranulomatous pyelonephritis

Stage Associations

This gene is associated with the following stages: