glutamate receptor, ionotropic, N-methyl D-aspartate 2B (GRIN2B)
Name: GRIN2B
Description: glutamate receptor, ionotropic, N-methyl D-aspartate 2B
Orgname: Homo sapiens
Status: 0
CurrentID: 0
Chromosome: 12
GeneticSource: genomic
MapLocation: 12p12
OtherAliases: MGC142178, MGC142180, NMDAR2B, NR2B, hNR3
OtherDesignations: N-methyl-D-aspartate receptor subunit 2B|glutamate receptor subunit epsilon-2
NomenclatureSymbol: GRIN2B
NomenclatureName: glutamate receptor, ionotropic, N-methyl D-aspartate 2B
NomenclatureStatus: Official
TaxID: 9606
Mim:
GenomicInfo:
GeneWeight: 32284
Summary: N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate receptors. NMDA receptor channel has been shown to be involved in long-term potentiation, an activity-dependent increase in the efficiency of synaptic transmission thought to underlie certain kinds of memory and learning. NMDA receptor channels are heteromers composed of three different subunits: NR1 (GRIN1), NR2 (GRIN2A, GRIN2B, GRIN2C, or GRIN2D) and NR3 (GRIN3A or GRIN3B). The NR2 subunit acts as the agonist binding site for glutamate. This receptor is the predominant excitatory neurotransmitter receptor in the mammalian brain. [provided by RefSeq]
ChrSort: 12
ChrStart: 13714409
UniProtein db: GRIN2B UniProt protein knowledge database
Ensembl db: GRIN2B Ensembl genome database
Complete information for GRIN2B gene (protein-coding), glutamate receptor, ionotropic, N-methyl D-aspartate 2B
Glutamate [NMDA] receptor subunit epsilon-2 is a protein that in humans is encoded by the GRIN2B gene.[1] ... GRIN2B may be a candidate gene for the neurodegenerative disorder ...
The world's first wiki where authorship really matters. Due credit and reputation for ... Mapping of the human NMDAR2B receptor subunit gene (GRIN2B) to chromosome 12p12. ...
GRIN2B gene to schizophrenia. The current meta-analysis covers all published association ... The GRIN2B gene, at 12p12 and 419 kb in size, consists of 13 ...
GRIN2B may be a candidate gene for the neurodegenerative disorder dentato-rubro-pallidoluysian atrophy (DRPLA). RefSeq annotates one representative transcript. ...
For this demonstration we will study expression of a key gene known as NR2B or Grin2b. This gene/mRNA/protein is crucial in learning and memory. ...
Mouse protein-coding gene Grin2b. Represented by 19 ESTs from 15 cDNA libraries. Corresponds to reference sequence NM_008171.3. [UniGene 2684545 - Mm.436649]
examined 16 reported SNPs across the NMDA receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B), five of which were identified in the Chinese population. ...
Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia. T Ohtsuki1, K Sakurai1, H Dou1, M Toru2, K Yamakawa-Kobayashi1 and T Arinami1 ...
'Mutation analysis of the NMDAR2B (GRIN2B) gene in schizophrenia.' on BiomedExperts. Find the right expert or researcher in 1.5 Million pre-calculated research ...
An association study of the N-methyl-D-aspartate receptor NR1 subunit gene (GRIN1) and NR2B subunit gene (GRIN2B) in schizophrenia with universal DNA microarray ...
Mouse Grin2b Chr6:135681645-136123529 bp, - strand has data for genome coordinates, mammalian orthology, sequences, phenotypes, polymorphisms, SNPs, ...
Number of SNPs in gene region: 4835 - Number of repeat elements ... Gene regulation - MicroRNAs elements associated with GRIN2B regulation: 3. Gene ontology ...
Search Term: GRIN2B (gene) Print page. Overview Data Correlations ... Survey of gene expression in ten common inbred strains of laboratory mouse. ...
N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate receptors. ... Search Term: GRIN2B (gene) Print page. Overview. glutamate receptor, ionotropic, N-methyl ...