Non-annotated gene. Preliminary data : if you are an author who wish to write a full paper/card on this gene, contribute in submission tool
Other Information
Locus ID:
NCBI: 116444
MIM: 606651
HGNC: 16768
Ensembl: ENSG00000116032
Variants:
dbSNP: 116444
ClinVar: 116444
TCGA: ENSG00000116032
COSMIC: GRIN3B
RNA/Proteins
| Gene ID | Transcript ID | Uniprot |
|---|---|---|
| ENSG00000116032 | ENST00000234389 | O60391 |
Expression (GTEx)
Pathways
References
| Pubmed ID | Year | Title | Citations |
|---|---|---|---|
| 28132660 | 2017 | GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders. | 14 |
| 28132660 | 2017 | GRIN3B missense mutation as an inherited risk factor for schizophrenia: whole-exome sequencing in a family with a familiar history of psychotic disorders. | 14 |
| 25768306 | 2015 | A naturally occurring null variant of the NMDA type glutamate receptor NR3B subunit is a risk factor of schizophrenia. | 10 |
| 25768306 | 2015 | A naturally occurring null variant of the NMDA type glutamate receptor NR3B subunit is a risk factor of schizophrenia. | 10 |
| 24814139 | 2014 | A recently-discovered NMDA receptor gene, GRIN3B, is associated with duration mismatch negativity. | 10 |
| 24814139 | 2014 | A recently-discovered NMDA receptor gene, GRIN3B, is associated with duration mismatch negativity. | 10 |
| 20153313 | 2010 | Expression of NR3B but not NR2D subunit of NMDA receptor in human blood lymphocytes can serve as a suitable peripheral marker for opioid addiction studies. | 6 |
| 20398908 | 2010 | Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients. | 34 |
| 20153313 | 2010 | Expression of NR3B but not NR2D subunit of NMDA receptor in human blood lymphocytes can serve as a suitable peripheral marker for opioid addiction studies. | 6 |
| 20398908 | 2010 | Comprehensive copy number variant (CNV) analysis of neuronal pathways genes in psychiatric disorders identifies rare variants within patients. | 34 |
| 19156168 | 2009 | Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis. | 49 |
| 20016182 | 2009 | Genetic variation in N-methyl-D-aspartate receptor subunit NR3A but not NR3B influences susceptibility to Alzheimer's disease. | 15 |
| 20016182 | 2009 | Genetic variation in N-methyl-D-aspartate receptor subunit NR3A but not NR3B influences susceptibility to Alzheimer's disease. | 15 |
| 19156168 | 2009 | Pharmacogenetics of antipsychotic response in the CATIE trial: a candidate gene analysis. | 49 |
| 20016182 | 2009 | Genetic variation in N-methyl-D-aspartate receptor subunit NR3A but not NR3B influences susceptibility to Alzheimer's disease. | 15 |
Citation
Dessen P
GRIN3B (glutamate ionotropic receptor NMDA type subunit 3B)
Atlas Genet Cytogenet Oncol Haematol. 2014-11-01
Online version: http://atlasgeneticsoncology.org/gene/64048/grin3b-(glutamate-ionotropic-receptor-nmda-type-subunit-3b)
