Source: CLINVAR

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		0.200 GeneticVariation CLINVAR Diagnostic Targeted Resequencing in 349 Patients with Drug-Resistant Pediatric Epilepsies Identifies Causative Mutations in 30 Different Genes. 27864847

2017
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		0.200 GeneticVariation CLINVAR Functional analysis of human Na(+)/K(+)-ATPase familial or sporadic hemiplegic migraine mutations expressed in Xenopus oocytes. 24921013

2014
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		0.200 GeneticVariation CLINVAR Crystal structure of the sodium-potassium pump at 2.4 A resolution. 19458722

2009
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2
CUI: C1832884
Disease: Hemiplegic migraine, familial type 1
Hemiplegic migraine, familial type 1 		0.200 GeneticVariation CLINVAR Epilepsy as part of the phenotype associated with ATP1A2 mutations. 18028407

2008