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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Grik4+
wild type
MGI:2430772
Summary 4 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
ht1
Grik4tm1(cre)Ksak/Grik4+ C57BL/6-Grik4tm1(cre)Ksak MGI:4360482
cn2
Grin2btm1Ksak/Grin2btm1Ksak
Grik4tm1(cre)Ksak/Grik4+
C57BL/6-Grin2btm1Ksak Grik4tm1(cre)Ksak MGI:4360481
cn3
Epha4tm2Kldr/Epha4tm2.1Kldr
Grik4tm1.1(cre)Slab/Grik4+
involves: C57BL/6 MGI:4398696
cn4
Grik4tm1(cre)Mim/Grik4+
Grin1tm1Mim/Grin1tm1Mim
involves: C57BL/6N MGI:4356068


Genotype
MGI:4360482
ht1
Allelic
Composition
Grik4tm1(cre)Ksak/Grik4+
Genetic
Background
C57BL/6-Grik4tm1(cre)Ksak
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grik4tm1(cre)Ksak mutation (0 available); any Grik4 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
normal phenotype
• mice are viable, fertile and do not display any overt behavioral or anotomic phenotype




Genotype
MGI:4360481
cn2
Allelic
Composition
Grin2btm1Ksak/Grin2btm1Ksak
Grik4tm1(cre)Ksak/Grik4+
Genetic
Background
C57BL/6-Grin2btm1Ksak Grik4tm1(cre)Ksak
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grik4tm1(cre)Ksak mutation (0 available); any Grik4 mutation (48 available)
Grin2btm1Ksak mutation (0 available); any Grin2b mutation (101 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• normal brain structure and morphology
• no overt behavioral phenotype
• reduced dendritic spine density
• increased detergent solubility of GluN2A subunit and PSD-95 in mutant CA3
• decreased F-actin content
• reduced GluN1 subunit from the postsynaptic site
• 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
• LTP is abolished at the commissural/associative-CA3 synapse and commissural-CA3 synapse
• mossy fiber-CA3 synapse are normal




Genotype
MGI:4398696
cn3
Allelic
Composition
Epha4tm2Kldr/Epha4tm2.1Kldr
Grik4tm1.1(cre)Slab/Grik4+
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Epha4tm2.1Kldr mutation (0 available); any Epha4 mutation (68 available)
Epha4tm2Kldr mutation (0 available); any Epha4 mutation (68 available)
Grik4tm1.1(cre)Slab mutation (2 available); any Grik4 mutation (48 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• mice exhibit normal long term potentiation and excitatory postsynaptic potential to theta burst- and tetanus-induced stimulation




Genotype
MGI:4356068
cn4
Allelic
Composition
Grik4tm1(cre)Mim/Grik4+
Grin1tm1Mim/Grin1tm1Mim
Genetic
Background
involves: C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Grik4tm1(cre)Mim mutation (0 available); any Grik4 mutation (48 available)
Grin1tm1Mim mutation (0 available); any Grin1 mutation (64 available)
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

behavior/neurological
• mutants are more susceptible to kainate induced tonic-clonic seizures than controls
• 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
• 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

nervous system
N
• dendritic arborization of CA3 pyramidal neurons is comparable to controls
• mutants are more susceptible to kainate induced tonic-clonic seizures than controls
• 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
• high frequency stimulation induces slowly decaying outward currents in CA3 pyramidal cells of control mice but not in mutants
• 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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last database update
07/08/2026
MGI 6.24
The Jackson Laboratory