Gene Expression: SCNN1A

Gene Data

  • Gene Symbol: SCNN1A
  • Gene ID: 6337
  • Synonyms: BESC2, ENaCa, ENaCalpha, SCNEA, SCNN1
  • Description: sodium channel, non-voltage-gated 1 alpha subunit
  • Database Refs: HGNC:10599, MIM:600228, Ensembl:ENSG00000111319, HPRD:02575, Vega:OTTHUMG00000168268
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 1 out of 17 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 24 diseases, scroll to view all:
  1. Cardiovascular system disease
  2. Congenital diaphragmatic hernia
  3. Cystic fibrosis
  4. Disease
  5. Disease of anatomical entity
  6. Disease of metabolism
  7. Endolymphatic hydrops
  8. Hypertension
  9. Inborn errors of metabolism
  10. Inborn errors renal tubular transport
  11. Kidney hypertrophy
  12. Labyrinthine disease
  13. Liddle syndrome
  14. Lower respiratory tract disease
  15. Lung disease
  16. Meniere's disease
  17. Newborn respiratory distress syndrome
  18. Peripheral vertigo
  19. Pseudohypoaldosteronism
  20. Pulmonary edema
  21. Respiratory failure
  22. Respiratory system disease
  23. Vascular disease
  24. Vestibular disease

Stage Associations

This gene is associated with the following stages: