Gene: ATP13A2 ×
Source: CURATED ×
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2 		0.440 Biomarker phenotype GENOMICS_ENGLAND Loss-of-function mutations in the ATP13A2/PARK9 gene cause complicated hereditary spastic paraplegia (SPG78). 28137957 2017
Entrez Id: 23400
Gene Symbol: ATP13A2
ATP13A2 		0.440 Biomarker phenotype GENOMICS_ENGLAND Recessively inherited parkinsonism: effect of ATP13A2 mutations on the clinical and neuroimaging phenotype. 21060012 2010