Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 Biomarker disease BEFREE We finaly prioritized 10 target genes for schizophrenia (CACNA1C, CLU, CSNK2B, GABBR1, GRIN2A, MAPK3, NOTCH4, SRR, TNF, and SYNGAP1). 30705251 2019
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 GeneticVariation disease GWASCAT Genome-Wide Association Study Detected Novel Susceptibility Genes for Schizophrenia and Shared Trans-Populations/Diseases Genetic Effect. 30285260 2019
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 GeneticVariation disease BEFREE SYNGAP1 loss-of-function variants are causally associated with intellectual disability, severe epilepsy, autism spectrum disorder and schizophrenia. 29580901 2018
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 GeneticVariation disease GWASCAT Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia. 28540026 2017
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 Biomarker disease BEFREE We sequenced the protein-encoding regions of DLG1, DLG2, DLG4, DLGAP1, DLGAP2, and SynGAP in 562 cases (370 SZ and 192 ASD patients) on the Ion PGM platform. 27271353 2016
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 GeneticVariation disease GWASCAT Genome-wide association study of schizophrenia in Ashkenazi Jews. 26198764 2015
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 Biomarker disease PSYGENET Reduced expression of the NMDA receptor-interacting protein SynGAP causes behavioral abnormalities that model symptoms of Schizophrenia. 19145222 2009
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 Biomarker disease MGD Reduced expression of the NMDA receptor-interacting protein SynGAP causes behavioral abnormalities that model symptoms of Schizophrenia. 19145222 2009
Entrez Id: 8831
Gene Symbol: SYNGAP1
SYNGAP1
0.630 GeneticVariation disease CLINVAR