Grin3b - glutamate receptor, ionotropic, NMDA3B Gene

Also Known as NR3B; GluN3B

Species: Mus musculus

Gene Type: protein coding
Gene ID: 170483

Summary

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). [provided by Alliance of Genome Resources, Apr 2022]

Grin3b Products (1)

mRNA Protein Name
NM_130455.2 NP_569722.1 glutamate receptor ionotropic, NMDA 3B precursor

Gene Ontology

  • Molecular Function
  • Biological Process
  • Cellular Component
Molecular Function GO Annotation Evidence References Source
contributes to calcium channel activity IMP
IMP: Inferred from mutant phenotype
14602821 MGI
Biological Process GO Annotation Evidence References Source
involved in protein insertion into membrane IMP
IMP: Inferred from mutant phenotype
14602821 MGI
involved in regulation of calcium ion transport IMP
IMP: Inferred from mutant phenotype
14602821 MGI
Cellular Component GO Annotation Evidence References Source
part of NMDA selective glutamate receptor complex IMP
IMP: Inferred from mutant phenotype
14602821 MGI
located in neuronal cell body IDA
IDA: Inferred from direct assay
11717388 MGI
located in neuronal cell body IMP
IMP: Inferred from mutant phenotype
14602821 MGI
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern
Protein Preferred Names Protein Names

glutamate receptor ionotropic, NMDA 3B

  • N-methyl-D-aspartate receptor subunit NR3B

  • NMDA receptor 4

  • NMDAR3B

  • glutamate [NMDA] receptor subunit 3B

  • nr4

Related Agents

  • Pre-clinical Phase

Pre-clinical Phase

Bioactive Molecules (1)
Cat. No. Product Name
Effect
Purity
Rare Diseases
HY-RS05807 GRIN3B Human Pre-designed siRNA Set A Pre-designed Set / Unkown

Orthologs Information

Species Symbol Source ID
Homo sapiens Grin3b NCBI NCBI:116444