Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.610 GeneticVariation disease BEFREE Monallelic pathogenic variants in ATP1A2 are associated with familial hemiplegic migraine type 2 (FHM2) and on rare occasions with alternating hemiplegia of childhood 1 (AHC1). 30690204 2020
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.610 Biomarker disease GENOMICS_ENGLAND Systematic analysis of three FHM genes in 39 sporadic patients with hemiplegic migraine. 18056581 2007
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.610 GeneticVariation disease UNIPROT Alternating hemiplegia of childhood or familial hemiplegic migraine? A novel ATP1A2 mutation. 15174025 2004
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.610 Biomarker disease GENOMICS_ENGLAND Novel mutations in the Na+, K+-ATPase pump gene ATP1A2 associated with familial hemiplegic migraine and benign familial infantile convulsions. 12953268 2003
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.610 Biomarker disease GENOMICS_ENGLAND Haploinsufficiency of ATP1A2 encoding the Na+/K+ pump alpha2 subunit associated with familial hemiplegic migraine type 2. 12539047 2003
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.610 CausalMutation disease CLINVAR
Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3 		0.300 Biomarker disease GENOMICS_ENGLAND De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. 22842232 2012