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Gene Expression: WFS1

Gene Data

  • Gene Symbol: WFS1
  • Gene ID: 7466
  • Synonyms: WFRS, WFS, WFSL
  • Description: Wolfram syndrome 1 (wolframin)
  • Database Refs: HGNC:12762, MIM:606201, Ensembl:ENSG00000109501, HPRD:05864, Vega:OTTHUMG00000090431
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 10 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 32 diseases, scroll to view all:
  1. Auditory system disease
  2. Carbohydrate metabolism disease
  3. Complex genetic disease
  4. Cranial nerve disease
  5. Diabetes insipidus
  6. Diabetes mellitus
  7. Diabetes mellitus type 1
  8. Disease
  9. Disease of anatomical entity
  10. Disease of metabolism
  11. Endocrine pancreas disease
  12. Endocrine system disease
  13. Eye and adnexa disease
  14. Eye disease
  15. Gastrointestinal system disease
  16. Genetic disease
  17. Globe disease
  18. Glucose metabolism disease
  19. Inner ear disease
  20. Kidney disease
  21. Nervous system disease
  22. Neurohypophyseal diabetes insipidus
  23. Neuropathy
  24. Nonsyndromic deafness
  25. Optic atrophy
  26. Optic nerve disease
  27. Pancreas disease
  28. Sensorineural hearing loss
  29. Sensory system disease
  30. Urinary system disease
  31. Visual pathway disease
  32. Wolfram syndrome

Stage Associations

This gene is associated with the following stages: