GRID2 (glutamate ionotropic receptor delta type subunit 2)

2003-05-01  

Identity

HGNC
LOCATION
4q22.1
LOCUSID
ALIAS
GluD2,SCAR18
FUSION GENES

Other Information

Locus ID:

NCBI: 2895
MIM: 602368
HGNC: 4576
Ensembl: ENSG00000152208

Variants:

dbSNP: 2895
ClinVar: 2895
TCGA: ENSG00000152208
COSMIC: GRID2

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000152208ENST00000282020O43424
ENSG00000152208ENST00000502699D6R9W8
ENSG00000152208ENST00000510992O43424
ENSG00000152208ENST00000512631D6R976
ENSG00000152208ENST00000513976H0YA12
ENSG00000152208ENST00000611049A0A087X043
ENSG00000152208ENST00000637838A0A1B0GW49

Expression (GTEx)

0
5
10
15

Pathways

PathwaySourceExternal ID
Neuroactive ligand-receptor interactionKEGGko04080
Long-term depressionKEGGko04730
Neuroactive ligand-receptor interactionKEGGhsa04080
Long-term depressionKEGGhsa04730

Protein levels (Protein atlas)

Not detected
Low
Medium
High

PharmGKB

Entity IDNameTypeEvidenceAssociationPKPDPMIDs
PA451257risperidoneChemicalClinicalAnnotationassociatedPD26905411

References

Pubmed IDYearTitleCitations
379440842024Clinical features, functional consequences, and rescue pharmacology of missense GRID1 and GRID2 human variants.1
379440842024Clinical features, functional consequences, and rescue pharmacology of missense GRID1 and GRID2 human variants.1
351592102022Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect.3
351592102022Neurodevelopmental Syndrome with Intellectual Disability, Speech Impairment, and Quadrupedia Is Associated with Glutamate Receptor Delta 2 Gene Defect.3
320650022021Association of Gene Variations in Ionotropic Glutamate Receptor and Attention-Deficit/Hyperactivity Disorder in the Chinese Population: A Two-Stage Case-Control Study.6
321706082021Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature.6
320650022021Association of Gene Variations in Ionotropic Glutamate Receptor and Attention-Deficit/Hyperactivity Disorder in the Chinese Population: A Two-Stage Case-Control Study.6
321706082021Autosomal recessive spinocerebellar ataxia 18 caused by homozygous exon 14 duplication in GRID2 and review of the literature.6
292079482017Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features.13
292079482017Homozygous GRID2 missense mutation predicts a shift in the D-serine binding domain of GluD2 in a case with generalized brain atrophy and unusual clinical features.13
269054112016Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes.23
270190352016Potential of GRID2 receptor gene for preventing TNF-induced neurodegeneration in autism.9
269054112016Antipsychotic pharmacogenomics in first episode psychosis: a role for glutamate genes.23
270190352016Potential of GRID2 receptor gene for preventing TNF-induced neurodegeneration in autism.9
251221452015Early-onset autosomal recessive cerebellar ataxia associated with retinal dystrophy: new human hotfoot phenotype caused by homozygous GRID2 deletion.23

Citation

Dessen P

GRID2 (glutamate ionotropic receptor delta type subunit 2)

Atlas Genet Cytogenet Oncol Haematol. 2003-05-01

Online version: http://atlasgeneticsoncology.org/gene/40753