Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes. 2842249

1988

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Chromosomal localization of human Na+, K+-ATPase alpha- and beta-subunit genes. 2842249

1988

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Alternating hemiplegia of childhood. 8496742

1993

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Alternating hemiplegia of childhood. 8496742

1993

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Alternating hemiplegia of childhood: clinical manifestations and long-term outcome. 11020638

2000

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Alternating hemiplegia of childhood: clinical manifestations and long-term outcome. 11020638

2000

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. 15260953

2004

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Mutations in the Na+/K+ -ATPase alpha3 gene ATP1A3 are associated with rapid-onset dystonia parkinsonism. 15260953

2004

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms. 16632466

2006

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Mutations Phe785Leu and Thr618Met in Na+,K+-ATPase, associated with familial rapid-onset dystonia parkinsonism, interfere with Na+ interaction by distinct mechanisms. 16632466

2006

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation. 19652145

2009

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Rapid-onset dystonia-parkinsonism in a child with a novel atp1a3 gene mutation. 19652145

2009

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism. 22534615

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR New triggers and non-motor findings in a family with rapid-onset dystonia-parkinsonism. 22534615

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. 22842232

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR De novo mutations in ATP1A3 cause alternating hemiplegia of childhood. 22842232

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study. 22850527

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Heterozygous de-novo mutations in ATP1A3 in patients with alternating hemiplegia of childhood: a whole-exome sequencing gene-identification study. 22850527

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia. 22924536

2013

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR ATP1A3 mutations in infants: a new rapid-onset dystonia-Parkinsonism phenotype characterized by motor delay and ataxia. 22924536

2013

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Psychiatric disorders in rapid-onset dystonia-parkinsonism. 22933743

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR Psychiatric disorders in rapid-onset dystonia-parkinsonism. 22933743

2012

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR The multiple faces of the ATP1A3-related dystonic movement disorder. 23483595

2013

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 GeneticVariation CLINVAR The multiple faces of the ATP1A3-related dystonic movement disorder. 23483595

2013

Entrez Id: 478
Gene Symbol: ATP1A3
ATP1A3
CUI: C0950123
Disease: Genetic Diseases, Inborn
Genetic Diseases, Inborn
0.100 CausalMutation CLINVAR Intermediate form between alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism. 24123283

2014