Click here to close Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari.

Summary Expression Phenotypes Gene Literature (200) GO Terms (137) Nucleotides (430) Proteins (122) Interactants (270) Wiki
XB-GENEPAGE-494199
???displayGene.symbol???:
 grin1

???displayGene.name???: 
glutamate ionotropic receptor NMDA type subunit 1

???displayGene.synonyms???
LOC108699855 , nmda1 , nmdar1 ( Nomenclature history )

???displayGene.geneFunction???
glutamate receptor channel component

AI Protein Function :
The grin1 gene encodes an NMDA-type glutamate receptor subunit that forms a ligand-gated ion channel permeable to calcium ions, functioning as a postsynaptic membrane-bound receptor involved in synapti...[+]


InterPro :
Peripla BP I, Glu/Gly-bd, Iontro rcpt, ANF lig-bd rcpt, [+]

???displayGene.geneInteractants???
Loading ...

Diseases: 


Disease Ontology:
autosomal dominant intellectual developmental disorder [+]

MIM:
NEURODEVELOPMENTAL DISORDER WITH OR WITHOUT HYPERKINETIC MOVEMENTS AND SEIZURES, [+]

External Links:
1/2
Loading gene data...
Please wait while we fetch the latest information
???displayGene.expression???                  Development Stages                                               Embryonic Tissues                                                                Adult Tissues
More Information
Xenbase Expression Details In situ images Single cell data at SPRING In situ: RNA-Seq:


Symbol legend: Blast sequence    View sequence    Literature or expression images   Hover cursor for info