Gene: GRIN1 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1 		0.600 GeneticVariation disease UNIPROT Novel homozygous missense variant of GRIN1 in two sibs with intellectual disability and autistic features without epilepsy. 28051072 2017
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1 		0.600 Biomarker disease GENOMICS_ENGLAND Novel homozygous missense variant of GRIN1 in two sibs with intellectual disability and autistic features without epilepsy. 28051072 2017
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1 		0.600 GeneticVariation disease UNIPROT Delineating the GRIN1 phenotypic spectrum: A distinct genetic NMDA receptor encephalopathy. 27164704 2016
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1 		0.600 Biomarker disease GENOMICS_ENGLAND De novo mutations in epileptic encephalopathies. 23934111 2013
Entrez Id: 2902
Gene Symbol: GRIN1
GRIN1 		0.600 GeneticVariation disease CLINVAR