Gene: DLG3 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.300 Biomarker disease CLINGEN A non-coding variant in the 5' UTR of DLG3 attenuates protein translation to cause non-syndromic intellectual disability. 27222290 2016
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.300 Biomarker disease CLINGEN Next-generation sequencing in X-linked intellectual disability. 25649377 2015
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.300 Biomarker disease CLINGEN X-exome sequencing in Finnish families with intellectual disability--four novel mutations and two novel syndromic phenotypes. 24721225 2014
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.300 Biomarker disease CLINGEN SAP102 mediates synaptic clearance of NMDA receptors. 23103165 2012
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.300 Biomarker disease CLINGEN A novel mutation in the DLG3 gene encoding the synapse-associated protein 102 (SAP102) causes non-syndromic mental retardation. 19795139 2010
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.300 Biomarker disease CLINGEN Synapse-associated protein 102/dlgh3 couples the NMDA receptor to specific plasticity pathways and learning strategies. 17344405 2007
Entrez Id: 1741
Gene Symbol: DLG3
DLG3 		0.300 Biomarker disease CLINGEN Mutations in the DLG3 gene cause nonsyndromic X-linked mental retardation. 15185169 2004