History:GENE:SCN9A    GENE:CSTB    

Gene Expression: ATP1A2

Gene Data

  • Gene Symbol: ATP1A2
  • Gene ID: 477
  • Synonyms: FHM2, MHP2
  • Description: ATPase, Na+/K+ transporting, alpha 2 polypeptide
  • Database Refs: HGNC:800, MIM:182340, Ensembl:ENSG00000018625, HPRD:01665, Vega:OTTHUMG00000024080
  • Links: Allen Brain Atlas,NCBI, GeneCards
Splicing Dynamics: DEXseq identifies changes in 0 out of 27 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 22 diseases, scroll to view all:
  1. Alternating hemiplegia of childhood
  2. Aphasia
  3. Argininosuccinic aciduria
  4. Brain disease
  5. Central nervous system disease
  6. Common migraine
  7. Communication disease
  8. Developmental disease of mental health
  9. Disease
  10. Disease of anatomical entity
  11. Disease of mental health
  12. Epilepsy
  13. Episodic ataxia
  14. Hemiplegia
  15. Infantile refsum disease
  16. Intellectual disability
  17. Language disease
  18. Migraine
  19. Nervous system disease
  20. Neuromuscular disease
  21. Sialuria
  22. Specific developmental disease

Stage Associations

This gene is associated with the following stages: