Gene: SNCA ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.110 GeneticVariation phenotype BEFREE On the other hand, α-synuclein deletion in both HD models increases autophagosome numbers and this is associated with a delayed onset of tremors and weight loss, two of the most prominent endophenotypes of the HD-like disease in mice. 22010050 2012
Entrez Id: 6622
Gene Symbol: SNCA
SNCA 		0.110 Biomarker phenotype HPO