History:GENE:UBQLN1    

Gene Expression: VSX1

Gene Data

  • Gene Symbol: VSX1
  • Gene ID: 30813
  • Synonyms: CAASDS, KTCN, KTCN1, PPCD, PPD, RINX
  • Description: visual system homeobox 1
  • Database Refs: HGNC:12723, MIM:605020, Ensembl:ENSG00000100987, HPRD:09232, Vega:OTTHUMG00000032111
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 8 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 28 diseases, scroll to view all:
  1. Alport syndrome
  2. Astigmatism
  3. Band keratopathy
  4. Chandler syndrome
  5. Corneal degeneration
  6. Corneal disease
  7. Corneal dystrophy
  8. Corneal ectasia
  9. Corneal edema
  10. Corneal granular dystrophy
  11. Disease
  12. Disease of anatomical entity
  13. Ectropion
  14. Eye and adnexa disease
  15. Eye disease
  16. Fuchs' endothelial dystrophy
  17. Glaucoma
  18. Globe disease
  19. Irregular astigmatism
  20. Juvenile glaucoma
  21. Keratoconus
  22. Macular corneal dystrophy
  23. Nervous system disease
  24. Refractive error
  25. Regular astigmatism
  26. Retinal degeneration
  27. Retinal disease
  28. Sensory system disease

Stage Associations

This gene is associated with the following stages: