Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
0.320 GeneticVariation disease BEFREE A mutation in the ATP1A2 sodium potassium ATPase pump gene has been described in a family in which familial hemiplegic migraine and benign familial infantile convulsions partly co-segregate. 15021241 2004
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
0.320 Biomarker disease GENOMICS_ENGLAND In this family, all available affected family members with FHM, benign familial infantile convulsions, or both, carry the ATP1A2 mutation. 12953268 2003
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
0.320 GeneticVariation disease BEFREE Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. 12953268 2003