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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Elfn1tm1.1Jaru
targeted mutation 1.1, Jun Aruga
MGI:5697443
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Elfn1tm1.1Jaru/Elfn1tm1.1Jaru involves: C57BL/6 MGI:5697457


Genotype
MGI:5697457
hm1
Allelic
Composition
Elfn1tm1.1Jaru/Elfn1tm1.1Jaru
Genetic
Background
involves: C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Elfn1tm1.1Jaru mutation (0 available); any Elfn1 mutation (30 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice show increased susceptibility to pentylenetetrazone (PTZ) induced seizures than wild-type mice, with 92% developing seizures compared to 57% of wild-type mice and with shorter latency to generalized seizure
• in the hole board test, mice show prolonged latencies to dipping their heads into all holes, whereas the total number of head dips does not differ
• in the elevated plus maze, mice spend a longer time in the open arms and show more entries into the open arms, however mice do not show reduced anxiety in the light-dark box test, suggesting increased impulsivity rather than reduced anxiety
• in the hole board test, mice show a lower total time of rearing
• mice show increased activity in home cages, mainly in the dark phase
• in the forced swimming test, mice show reduced immobility time
• however, mice show normal prepulse inhibition and pain sensitivity
• in the light-dark box transition test, the total distance travelled and total number of transitions are larger in mutants
• mice show increased total distance traveled in the elevated plus maze and hole board tests
• mice exhibit epileptic seizures during routine handling
• handling seizures are seen beginning at 11 weeks of age and the percentage of affected mice peaks (at about 80%) at 5 months

nervous system
• mice show increased susceptibility to pentylenetetrazone (PTZ) induced seizures than wild-type mice, with 92% developing seizures compared to 57% of wild-type mice and with shorter latency to generalized seizure
• mice exhibit epileptic seizures during routine handling
• handling seizures are seen beginning at 11 weeks of age and the percentage of affected mice peaks (at about 80%) at 5 months
• small but significant decrease in GluR1a-positive spine density at 4 months of age
• EEG activity indicates the presence of frequent sharp waves not seen in wild-type mice
• impaired presynaptic form of plasticity
• synapses do not show facilitation and the 3rd, 4th, and 5th excitatory postsynaptic currents (EPSCs) are depressed indicating impaired short-term plasticity at excitatory synapses onto oriens lacunosum moleculare neurons
• however, short-term plasticity of synaptic inputs to pyramidal neurons are normal
• LTP at pyramidal neuron- onto oriens lacunosum moleculare neuron synapses is impaired
• a brief train of afferent stimulation induces short-term depression rather than short-term facilitation at CA1 pyramidal neuron- onto oriens lacunosum moleculare neuron synapses





Contributing Projects:
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
05/14/2024
MGI 6.23
The Jackson Laboratory