Gene Expression: NR3C2

Gene Data

  • Gene Symbol: NR3C2
  • Gene ID: 4306
  • Synonyms: MCR, MLR, MR, NR3C2VIT
  • Description: nuclear receptor subfamily 3, group C, member 2
  • Database Refs: HGNC:7979, MIM:600983, Ensembl:ENSG00000151623, HPRD:02991, Vega:OTTHUMG00000161455
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 9 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 53 diseases, scroll to view all:
  1. Adenoma
  2. Adrenal cortex disease
  3. Adrenal gland disease
  4. Adrenal gland hyperfunction
  5. Adrenal hyperplasia
  6. Apparent mineralocorticoid excess syndro
  7. Benign neoplasm
  8. Brachydactyly
  9. Carbohydrate metabolism disease
  10. Cardiovascular system disease
  11. Cerebrovascular accident
  12. Congestive heart failure
  13. Conn syndrome
  14. Cushing syndrome
  15. Diabetes mellitus
  16. Diastolic heart failure
  17. Disease
  18. Disease of anatomical entity
  19. Disease of cellular proliferation
  20. Disease of metabolism
  21. Endocrine pancreas disease
  22. Endocrine syndrome
  23. Endocrine system disease
  24. Essential hypertension
  25. Extrinsic cardiomyopathy
  26. Gastrointestinal system disease
  27. glucocorticoid-remediable aldosteronism
  28. Glucose metabolism disease
  29. Gynecomastia
  30. Heart disease
  31. Heart failure
  32. Hyperaldosteronism
  33. Hypertension
  34. Hypertrophy of breast
  35. Hypokalemia
  36. Inborn errors of metabolism
  37. Inborn errors renal tubular transport
  38. Inborn errors steroid metabolism
  39. Ischemia
  40. Kidney disease
  41. Kidney failure
  42. Liddle syndrome
  43. Lymphoma
  44. Mineral metabolism disease
  45. Myocardial infarction
  46. Myocardial ischemia
  47. Pancreas disease
  48. Proteinuria
  49. Pseudohypoaldosteronism
  50. Secondary hypertension
  51. Systolic heart failure
  52. Urinary system disease
  53. Vascular disease

Stage Associations

This gene is associated with the following stages: