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FLASH GENE
Symbol GRIN3A contributors: mct - updated : 07-10-2015
HGNC name glutamate receptor, ionotropic, N-methyl-D-aspartate 3A
HGNC id 16767
Location 9q31.1      Physical location : 104.331.634 - 104.500.862
Synonym name
  • glutamate [NMDA] receptor subunit 3A
  • N-methyl-D-aspartate receptor subtype 3A
  • Synonym symbol(s) NR3A, KIAA1973, NMDAR-L, NMDAR3A, FLJ45414
    DNA
    TYPE functioning gene
    STRUCTURE 169.23 kb     9 Exon(s)
    10 Kb 5' upstream gene genomic sequence study
    MAPPING cloned Y linked N status confirmed
    RNA
    TRANSCRIPTS type messenger
    identificationnb exonstypebpproduct
    ProteinkDaAAspecific expressionYearPubmed
    9 - 7771 - 1115 - -
    EXPRESSION
    Type widely
       expressed in (based on citations)
    organ(s)
    SystemOrgan level 1Organ level 2Organ level 3Organ level 4LevelPubmedSpeciesStageRna symbol
    Endocrineadrenal gland   predominantly
    Nervousbrainforebraincerebral lobeoccipital lobe 
     brainforebraincerebral cortexoccipital cortex 
     nerve   highly
    Reproductivefemale systemuteruscervix highly
    tissue
    SystemTissueTissue level 1Tissue level 2LevelPubmedSpeciesStageRna symbol
    Connectivebone   
    Nervouscentral   
    cell lineage
    cell lines
    fluid/secretion
    at STAGE
    physiological period fetal
    Text brain
    PROTEIN
    PHYSICAL PROPERTIES
    STRUCTURE
    motifs/domains
  • a 26 aa signal peptide
  • ten putative sites for glycosylation
  • three potential sites for protein kinase C
  • an extracellular ligand binding domain
  • four membrane segments
  • conjugated GlycoP
    mono polymer heteromer , trimer , complex
    HOMOLOGY
    interspecies homolog to rattus Nr3a
    ortholog to murine Nr3a
    intraspecies homolog to GRIN3B
    Homologene
    FAMILY
  • glutamate-gated ion channel family
  • N-methyl-D-asparate family
  • CATEGORY regulatory , receptor membrane , transport channel
    SUBCELLULAR LOCALIZATION     plasma membrane
    text postsynaptic membrane
    basic FUNCTION
  • excitatory glycine receptor
  • involved in the development of synaptic elements by modulating NMDAR activity
  • ligand-gated ion channel (Ca2+) transporting, when bound to glutamate and Mg2+ released
  • suppressing glutamate induced currents, a NMDA receptor dominant negative
  • GRIN3A prevents the activity-dependent stabilization of synapses thereby promoting spine pruning, suggesting that GRIN3A expression operates as a molecular signal for controlling the extent and timing of synapse maturation
  • CELLULAR PROCESS
    PHYSIOLOGICAL PROCESS development , nervous system
    text ion transport
    PATHWAY
    metabolism
    signaling
    a component
  • N-glycosylated
  • forming heteromeric channel of a zeta subunit (GRIN1), a epsilon subunit (GRIN2A, GRIN2B, GRIN2C or GRIN2D) and a third subunit (GRIN3A or GRIN3B)
  • found in a complex with GRIN1, GRIN2A or GRIN2B and PPP2CB
  • INTERACTION
    DNA
    RNA
    small molecule metal binding,
  • Mg2+
  • protein
  • GRIN1 to form excitatory glutamate receptor
  • PPP2CB
  • co-expression of both GRIN3A and GRIN3B subunits is essential for the dominant negative properties on Ca(2+) mobilization through acquired functional NMDAR channels into mitochondria
  • GRIN3A binds GIT1, a postsynaptic scaffold that assembles actin regulatory complexes, including the RAC1 guanine nucleotide exchange factor ARHGEF7, to promote RAC1 activation in spines
  • interaction of GRIN3A with PACSIN1, which prevents the endocytosis of endogenous GRIN3A
  • cell & other
    REGULATION
    activated by the artificial glutamate analog N-methyl D-aspartate (selectively)
    dual agonists glutamate,glycine
    ASSOCIATED DISORDERS
    corresponding disease(s)
    Susceptibility
  • to schizophrenia
  • to Alzheimer disease (AD)
  • Variant & Polymorphism other
  • rare mutations in the GRIN3A gene may contribute to the pathogenesis of schizophrenia in certain patients (Shen 2010)
  • G allele was present at a higher rate than the A allele at position 3723 in AD patients compared with normal groups (
  • Candidate gene strong candidate for involvement in the etiology of nicotine dependence (Ma 2010)
    Marker
    Therapy target
    ANIMAL & CELL MODELS
    Nr3a knockout mice (Das)