Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
0.340 GeneticVariation disease BEFREE A de novo nonsense variant in GRIN2B was identified in an ASD case adding to the growing evidence that this is an important risk gene for the disorder. 24126926 2015
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
0.340 GeneticVariation disease BEFREE GRIN2B alterations, including mutation and gene disruption by apparently balanced chromosomal rearrangements, have been described in patients with intellectual disability and autism spectrum disorder. 23918416 2014
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
0.340 GeneticVariation disease BEFREE Here, we identified two de novo mutations in patients with sporadic SCZ in GRIN2A and one de novo mutation in GRIN2B in a patient with ASD. 22833210 2013
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
0.340 Biomarker disease BEFREE Family based association of GRIN2A and GRIN2B with Korean autism spectrum disorders. 22326929 2013
Entrez Id: 2904
Gene Symbol: GRIN2B
GRIN2B
0.340 Biomarker disease CTD_human Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations. 21572417 2011