Gene: ATXN2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6311
Gene Symbol: ATXN2
ATXN2 		0.020 GeneticVariation disease BEFREE This family expands the phenotypic spectrum of early onset SCA2 and points out the importance of considering SCA2 gene analysis in children with progressive neurological impairment and abnormal movements with or without polyphagia. 18297329 2008
Entrez Id: 6311
Gene Symbol: ATXN2
ATXN2 		0.020 GeneticVariation disease LHGDN Homozygous SCA 2 mutations changes phenotype and hastens progression. 18265007 2008