Gene Expression: GJA1

Gene Data

  • Gene Symbol: GJA1
  • Gene ID: 2697
  • Synonyms: AVSD3, CMDR, CX43, DFNB38, GJAL, HLHS1, HSS, ODDD
  • Description: gap junction protein, alpha 1, 43kDa
  • Database Refs: HGNC:4274, MIM:121014, Ensembl:ENSG00000152661, HPRD:00414, Vega:OTTHUMG00000015479
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 6 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 78 diseases, scroll to view all:
  1. Acute myocardial infarction
  2. angle-closure glaucoma
  3. Arterial occlusive disease
  4. Arteriosclerosis
  5. Arteriosclerotic cardiovascular disease
  6. Astrocytoma
  7. Atherosclerosis
  8. Auditory system disease
  9. Bone development disease
  10. Brain cancer
  11. Brain disease
  12. Brain neoplasm
  13. Cancer
  14. Carbohydrate metabolism disease
  15. Cardiovascular system disease
  16. Cell type cancer
  17. Central nervous system cancer
  18. Central nervous system disease
  19. Central nervous system neoplasm
  20. Chagas disease
  21. Clouston syndrome
  22. Complex genetic disease
  23. Congenital heart defect
  24. Congestive heart failure
  25. Dental enamel hypoplasia
  26. Diabetes mellitus
  27. Dilated cardiomyopathy
  28. Disease
  29. Disease of anatomical entity
  30. Disease of cellular proliferation
  31. Disease of metabolism
  32. Dysostosis
  33. Endocrine pancreas disease
  34. Endocrine system disease
  35. Extrinsic cardiomyopathy
  36. Eye and adnexa disease
  37. Eye disease
  38. Gastrointestinal system disease
  39. Genitourinary cancer
  40. Germ cell cancer
  41. Glaucoma
  42. Glioma
  43. Globe disease
  44. Glucose metabolism disease
  45. Hallermann-Streiff syndrome
  46. Heart disease
  47. Heart failure
  48. Hypertension
  49. Hypoplastic left heart syndrome
  50. Inner ear disease
  51. Intracranial neoplasm
  52. Intrinsic cardiomyopathy
  53. Ischemia
  54. Keratosis
  55. Malignant glioma
  56. Malignant intracranial neoplasm
  57. Medical disorder
  58. Microphthalmia
  59. Musculoskeletal system disease
  60. Myocardial infarction
  61. Myocardial ischemia
  62. Nervous system cancer
  63. Nervous system disease
  64. Organ system cancer
  65. Palmoplantar keratosis
  66. Pancreas disease
  67. Physical disorder
  68. Reproductive organ cancer
  69. Reproductive system disease
  70. Retinal degeneration
  71. Retinal disease
  72. Sensorineural hearing loss
  73. Sensory system disease
  74. Syndactyly
  75. Synostosis
  76. Teeth hard tissue disease
  77. Tetralogy of Fallot
  78. Vascular disease

Stage Associations

This gene is associated with the following stages: