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GRIN2B - glutamate ionotropic receptor NMDA type subunit 2B
- Synonym(s) : GluN2B
- Previous symbols and names : NMDAR2B, glutamate receptor, ionotropic, N-methyl D-aspartate 2B
- Type : gene with protein product
- Chromosomal location : 12p13.1
- OMIM: 138252
- HGNC: 4586
- UniProtKB: Q13224
- Genatlas: GRIN2B
- GenCC: GRIN2B
- Ensembl: ENSG00000273079
- IUPHAR-DB: 457
- Reactome: Q13224
- LOVD: GRIN2B
Diseases list
- Disease-causing germline mutation(s) in Autosomal dominant non-syndromic intellectual disability
ORPHA:178469 
- Disease-causing germline mutation(s) in GRIN2B-related developmental delay, intellectual disability and autism spectrum disorder
ORPHA:589547 - Disease-causing germline mutation(s) (gain of function) in Infantile spasms syndrome
ORPHA:3451
: AssessedAdditional information
Patient-centred resources for this gene
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