Gene: GRIN2A ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 2903
Gene Symbol: GRIN2A
GRIN2A 		0.300 Biomarker disease CTD_human GRIN2A mutations cause epilepsy-aphasia spectrum disorders. 23933818 2013
Entrez Id: 2903
Gene Symbol: GRIN2A
GRIN2A 		0.300 Biomarker disease CTD_human Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes. 20890276 2010