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Protein Coding Gene : Grin3b glutamate receptor, ionotropic, NMDA3B

Primary Identifier  MGI:2150393 Organism  mouse, laboratory
Chromosome  10 NCBI Gene Number  170483
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Contributes to calcium channel activity. Involved in protein insertion into membrane and regulation of calcium ion transport. Located in neuronal cell body. Part of NMDA selective glutamate receptor complex. Is expressed in central nervous system; gut gland; retina; and testis. Orthologous to human GRIN3B (glutamate ionotropic receptor NMDA type subunit 3B).
PHENOTYPE: Mice homozygous for a null allele show a mild impairment in motor learning or coordination, reduced home cage activity, a highly increased social interaction with familiar cagemates in their home cage but moderately increased anxiety-like behavior and reduced social interaction in a new environment. [provided by MGI curators]
  • synonyms:
  • NR3B,
  • glutamate receptor, ionotropic, NMDA3B,
  • Grin3b

Features --> Cross References

Genome

Sequence Feature Displayer

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0 Canonical

0 CDSs

0 Exons

0 Genomic Clusters

2 Involved In Mutations

0 Strain

0 Transcripts

0 Transgenic Expressors

0 UTRs

Canonical gene --> CDSs in specific strains.

Canonical gene --> Exons in specific strains

Canonical gene --> Strain-specific IDs, biotypes, and locations

Canonical gene --> Transcripts in specific strains.

Features --> Overlapping features

Proteins

Gene --> Proteins

Function

Mouse features --> Functions (GO terms)

Homology

Genes --> Homologs

Interactions

0 Pathways

0 Targeted By

Gene --> Protein-Protein Interactions

Expression

Gene --> Expression annotations

Phenotype

Genes/Features --> Phenotypes (MP terms)

Disease

Mouse features --> Human diseases

Literature

Mouse features --> Publications

 

Other

0 Driver For