Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6854
Gene Symbol: SYN2
SYN2
0.260 GeneticVariation disease BEFREE Synapsin II (SynII) deletion produces epileptic seizures and overexcitability in neuronal networks. 30858140 2019
Entrez Id: 6854
Gene Symbol: SYN2
SYN2
0.260 Biomarker disease BEFREE Together, our results demonstrate that SynII regulates the time course of GABAergic release, and that this SynII function is dependent on the interneuron subtype.<b>SIGNIFICANCE STATEMENT</b> Deletion of the neuronal protein synapsin II (SynII) leads to the development of epilepsy, probably due to impairments in inhibitory synaptic transmission. 28087765 2017
Entrez Id: 6854
Gene Symbol: SYN2
SYN2
0.260 Biomarker disease BEFREE Mutations in Synapsin (SYN) genes, particularly SYN1 and SYN2, have been recently associated with ASD and epilepsy in humans. 28922833 2017
Entrez Id: 6854
Gene Symbol: SYN2
SYN2
0.260 GeneticVariation disease BEFREE Evidence has shown linkage disequilibrium between rs3755724 (-55C/T) of this gene with synapsin 2 (SYN2) rs3773364 and peroxisome proliferator-activated G receptor (PPARG) rs2920502 loci, which contribute to epilepsy in Caucasians. 25595263 2015
Entrez Id: 6854
Gene Symbol: SYN2
SYN2
0.260 GeneticVariation disease BEFREE Our study indicated that SYN2 rs3773364 A>G polymorphism is not a risk factor for susceptibility to epilepsy. 21465568 2011
Entrez Id: 6854
Gene Symbol: SYN2
SYN2
0.260 Biomarker disease BEFREE According to the results obtained, SYN2 "AG" genotype frequency was significantly higher in patients with epilepsy versus control subjects in north Indian population (P = 0.02, OR = 1.55, 95% CI = 1.06-2.26). 20034013 2010
Entrez Id: 6854
Gene Symbol: SYN2
SYN2
0.260 Biomarker disease MGD