Gene Expression: GCNT2

Gene Data

  • Gene Symbol: GCNT2
  • Gene ID: 2651
  • Synonyms: CCAT, CTRCT13, GCNT2C, GCNT5, IGNT, II, NACGT1, NAGCT1, ULG3, bA360O19.2, bA421M1.1
  • Description: glucosaminyl (N-acetyl) transferase 2, I-branching enzyme (I blood group)
  • Database Refs: HGNC:4204, MIM:600429, Ensembl:ENSG00000111846, HPRD:02695, Vega:OTTHUMG00000014244
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 3 out of 13 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. Aniridia
  2. Anisometropia
  3. Bacterial conjunctivitis
  4. beta-mannosidosis
  5. Coats disease
  6. Coloboma
  7. Complex genetic disease
  8. Congenital nystagmus
  9. Connective tissue neoplasm
  10. Corneal dystrophy
  11. Cortical blindness
  12. Cutaneous mastocytosis
  13. Degenerative myopia
  14. Disease
  15. Disease of anatomical entity
  16. Exfoliation syndrome
  17. Eye degenerative disease
  18. Fucosidosis
  19. Glaucoma
  20. Iris disease
  21. Mannosidase deficiency disease
  22. Mast cell neoplasm
  23. Mastocytosis
  24. Microphthalmia
  25. Myopia
  26. Ophthalmia neonatorum
  27. Optic nerve disease
  28. Pathologic nystagmus
  29. Penicilliosis
  30. Refractive error
  31. Retinal degeneration
  32. Retinal telangiectasia
  33. Soft tissue cancer
  34. Visual cortex disease
  35. Visual pathway disease

Stage Associations

This gene is associated with the following stages: