Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.060 Biomarker group BEFREE Prompted by the recent identification of neuronal aggregates of α-synuclein in another lysosomal storage disease, Krabbe's disease, we propose the idea that a similar connection exists between adult synucleinopathies and Krabbe's. 27638614 2016
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.060 Biomarker group BEFREE This study suggests a possible role of NAGLU in susceptibility to PD while extending evidence for α-synuclein aggregation in the brain in lysosomal storage disorders. 22102531 2012
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.060 Biomarker group BEFREE Loss in GCase activity did not immediately raise SNCA concentrations, but first led to neuronal ubiquitinopathy and axonal spheroids, a phenotype shared with other lysosomal storage disorders. 21472771 2011
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.060 Biomarker group BEFREE We have performed an exhaustive literature search and found that additional lysosomal storage disorders might be associated with Parkinson's disease, based on case reports, the appearance of pathological features such as α-synuclein deposits in the brain, and substantia nigra pathology. 21618611 2011
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.060 Biomarker group BEFREE An impairment of the autophagic pathway was demonstrated by the inefficient degradation of exogenous aggregate-prone proteins (i.e. expanded huntingtin and mutated alpha-synuclein) in cells from LSD mice. 17913701 2008
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.060 Biomarker group BEFREE In addition, the accumulation of alpha-synuclein may also be a condition that is common to lysosomal storage diseases and adrenoleukodystrophies that show an enhanced expression of this protein upon the elevation of stored lipids. 17653558 2007
Entrez Id: 6622
Gene Symbol: SNCA
SNCA
0.060 AlteredExpression group LHGDN In addition, the accumulation of alpha-synuclein may also be a condition that is common to lysosomal storage diseases and adrenoleukodystrophies that show an enhanced expression of this protein upon the elevation of stored lipids. 17653558 2007