Gene Expression: SEPN1

Gene Data

  • Gene Symbol: SEPN1
  • Gene ID: 57190
  • Synonyms: CFTD, MDRS1, RSMD1, RSS, SELN
  • Description: selenoprotein N, 1
  • Database Refs: HGNC:15999, MIM:606210, Ensembl:ENSG00000162430, HPRD:05867, Vega:OTTHUMG00000007375
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 2 out of 13 exons in this gene. (More about DEXSeq here)

Cluster Associations

This gene is associated with the following clusters: No Clusters were found

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 22 diseases, scroll to view all:
  1. Atrophic muscular disease
  2. Bethlem myopathy
  3. Central core myopathy
  4. Congenital muscular dystrophy
  5. Congenital structural myopathy
  6. Cranial nerve disease
  7. Disease
  8. Disease of anatomical entity
  9. Endocrine syndrome
  10. Malignant hyperthermia
  11. Muscle tissue disease
  12. Muscular disease
  13. Muscular dystrophy
  14. Musculoskeletal system disease
  15. Myopathy
  16. Nemaline myopathy
  17. Nervous system disease
  18. Neuromuscular disease
  19. Neuropathy
  20. Ocular motility disease
  21. Ophthalmoplegia
  22. Ullrich congenital muscular dystrophy

Stage Associations

This gene is associated with the following stages: No Stages were found