normal phenotype
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• mice are viable, fertile and do not display any overt behavioral or anotomic phenotype
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Analysis Tools|
Allele Symbol Allele Name Allele ID |
Grik4+ wild type MGI:2430772 |
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| Summary |
4 genotypes
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
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• mice are viable, fertile and do not display any overt behavioral or anotomic phenotype
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
| N |
• normal brain structure and morphology
• no overt behavioral phenotype
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• reduced dendritic spine density
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• increased detergent solubility of GluN2A subunit and PSD-95 in mutant CA3
• decreased F-actin content
• reduced GluN1 subunit from the postsynaptic site
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• NMDAR-mediated synaptic currents are abolished in three excitatory CA3 synapses: the commissural/associative-CA3 synapse, commissural-CA3 synapse, and mossy fiber-CA3 synapse
• reduced but detectable extrasynaptic NMDAR-mediated currents
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• LTP is abolished at the commissural/associative-CA3 synapse and commissural-CA3 synapse
• mossy fiber-CA3 synapse are normal
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
| N |
• mice exhibit normal long term potentiation and excitatory postsynaptic potential to theta burst- and tetanus-induced stimulation
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| ♀ | phenotype observed in females |
| ♂ | phenotype observed in males |
| N | normal phenotype |
Increased susceptibility to kainate-induced tonic-clonic seizures in Grin1tm1Mim/Grin1tm1Mim Grik4tm1(cre)Mim/Grik4+ mice
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• mutants are more susceptible to kainate induced tonic-clonic seizures than controls
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• intraperitoneal injection of 8 mg/kg kainate results in loss of postural reflex along with seizures in mutants within 1 hour but not in controls
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• intraperitoneal injection of 8 mg/kg kainate induces seizures in 8 week-old mutants within 1 hour but not in wild-type controls; higher doses cause seizures in all genotypes, but latency in mutants is significantly shorter
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| N |
• dendritic arborization of CA3 pyramidal neurons is comparable to controls
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• mutants are more susceptible to kainate induced tonic-clonic seizures than controls
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• intraperitoneal injection of 8 mg/kg kainate induces seizures in 8 week-old mutants within 1 hour but not in wild-type controls; higher doses cause seizures in all genotypes, but latency in mutants is significantly shorter
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• high frequency stimulation induces slowly decaying outward currents in CA3 pyramidal cells of control mice but not in mutants
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• field potential recordings in the CA3 region at 8 weeks reveal characteristic spikes with large amplitudes that are not observed in controls; these spikes originate in the CA3 and CA1 pyramidal cell layers but not in the dentate gyrus
• similar results are obtained when ablation of Grin1 in the CA3 region is accomplished using injection of adenoviral cre
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 07/08/2026 MGI 6.24 |
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