History:GENE:CAPN2    

Gene Expression: FBN2

Gene Data

  • Gene Symbol: FBN2
  • Gene ID: 2201
  • Synonyms: CCA, DA9
  • Description: fibrillin 2
  • Database Refs: HGNC:3604, MIM:612570, Ensembl:ENSG00000138829, HPRD:00416, Vega:OTTHUMG00000163082
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 64 out of 68 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 35 diseases, scroll to view all:
  1. angle-closure glaucoma
  2. Bone development disease
  3. Calcium metabolism disease
  4. Campylobacteriosis
  5. Cardiovascular system disease
  6. Connective tissue disease
  7. Cutis laxa
  8. Dental pulp calcification
  9. Disease
  10. Disease of anatomical entity
  11. Distal arthrogryposis
  12. Dysostosis
  13. Erythema infectiosum
  14. Genetic disease
  15. Heart disease
  16. Heart valve disease
  17. Heart valve prolapse
  18. Hypercalcemia
  19. Hyperparathyroidism
  20. Intracranial aneurysm
  21. Keratoconus
  22. Larsen syndrome
  23. Loeys-Dietz syndrome
  24. Marfan syndrome
  25. Mineral metabolism disease
  26. Mitral valve disease
  27. Mitral valve prolapse
  28. Monogenic disease
  29. Musculoskeletal system disease
  30. Parathyroid gland disease
  31. Supravalvular aortic stenosis
  32. Syndactyly
  33. Synostosis
  34. Ventricular septal defect
  35. Viral exanthem

Stage Associations

This gene is associated with the following stages: