Gene: ATP1A2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.130 GeneticVariation phenotype BEFREE An Infant With Epilepsy and Recurrent Hemiplegia due to Compound Heterozygous Variants in ATP1A2. 28811059 2017
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.130 Biomarker phenotype BEFREE Patients with FHM2 may also present without hemiplegia. 24096472 2014
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.130 GeneticVariation phenotype BEFREE In two of the six remaining patients the attacks were no longer associated with hemiplegia; one of them had an ATP1A2 gene mutation (E120A). 20974584 2011
Entrez Id: 477
Gene Symbol: ATP1A2
ATP1A2 		0.130 Biomarker phenotype HPO