Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.440 Biomarker GENOMICS_ENGLAND Heterozygous variants of GRIN1, encoding the GluN1 subunit of the NMDA receptor, have been reported in patients with neurodevelopmental disorders including epileptic encephalopathy, severe intellectual disability, and movement disorders. 28051072

2017

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.440 Biomarker GENOMICS_ENGLAND Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. 27164704

2016

Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1
CUI: C0543888
Disease: Epileptic encephalopathy
Epileptic encephalopathy
0.440 Biomarker GENOMICS_ENGLAND De novo mutations in epileptic encephalopathies. 23934111

2013