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Gene : GRIN3A Homo sapiens

Name  ? glutamate ionotropic receptor NMDA type subunit 3A Cytological Location  9q31.1
Brief Description  glutamate ionotropic receptor NMDA type subunit 3A
description  This gene encodes a subunit of the N-methyl-D-aspartate (NMDA) receptors, which belong to the superfamily of glutamate-regulated ion channels, and function in physiological and pathological processes in the central nervous system. This subunit shows greater than 90% identity to the corresponding subunit in rat. Studies in the knockout mouse deficient in this subunit suggest that this gene may be involved in the development of synaptic elements by modulating NMDA receptor activity. [provided by RefSeq, Jul 2008]
  • synonyms:
  • OTTHUMG00000020387,
  • glutamate receptor, ionotropic, N-methyl-D-aspartate 3A,
  • GluN3A,
  • NR3A,
  • NMDAR-L,
  • uc004bbp.3,
  • HGNC:16767,
  • NM_133445,
  • GRIN3A,
  • GluN3A
  • identifiers:
  • 116443,
  • ENSG00000198785,
  • GRIN3A

Genome feature

Region: gene ? Length: 169229  
Location: 9:101569352-101738580 reverse strand Cyto location: 9q31.1


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

225 SN Ps

5 Cross References

14 Data Sets

20 Homologues

0 Located Features

90 Rna Seq Results