×
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