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Phenotypes Associated with This Genotype
Genotype
MGI:3759301
Allelic
Composition
Dlgap3tm1Gfng/Dlgap3tm1Gfng
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Dlgap3tm1Gfng mutation (1 available); any Dlgap3 mutation (84 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• grooming behavior and anxiety-related behaviors are reduced following treatment with fluoxetine for 6 days whereas grooming behavior in similarly treated wild-type mice is unchanged
• treatment with fluoxetine for 6 days reduced the number of sleeping bouts and increased the sleeping time per bout
• however, a single treatment of fluoxetine has no effect on grooming behavior
• in a dark-light test, mice take more time to cross from the dark to the lit chamber and spent less time in the lit chamber compared to wild-type mice
• however, activity levels overall are normal and treatment with fluoxetine for 6 days reduces anxiety-related behaviors in a dark-light test without affecting total activity levels
• in an elevated zero maze test, mice take longer to cross into the open areas and spent less time exploring than do wild-type mice
• in an open field test mice spend more time long walls and spend less time exploring than do wild-type mice
• however, activities along the walls and in corners is normal
• mice exhibit increased grooming bouts and spend more time self-grooming prior to lesion formation than do wild-type mice
• however, grooming behavior is reduced following treatment with fluoxetine for 6 days whereas grooming behavior in similarly treated wild-type mice is unchanged
• mice sleep less during normal sleeping periods and sleep more during active times compared to wild-type mice
• mice have increased sleeping bouts but the time slept per bout was reduced relative to in wild-type mice
• however, treatment with fluoxetine for 6 days reduces the number of sleeping bouts and increases the sleeping time per bout

nervous system
• the thickness of the dense layer, but not the light layer, in postsynaptic densities of cortico-striatal synapses is reduced compared to in wild-type mice
• field excitatory postsynaptic potential (fEPSP) in the presence of picrotoxin is decreased compared to in wild-type mice
• NMDAR-dependent fEPSP amplitudes are increased relative to in wild-type mice
• however, axon excitability and presynaptic function are normal as is CA3-CA1 hippocampal basal synaptic transmission
• NMDAR-dependent fEPSP amplitudes are increased relative to in wild-type mice
• however, CA3-CA1 hippocampal basal synaptic transmission is normal

integument
• by 4 to 6 months, all mice develop lesions on their heads, neck and snout regions
• lesions begin as hairless skin under eyes, or swelling of the snout and progress to relatively symmetrical bilateral lesions encompassing large parts of the head and neck
• skin with lesions contains increased lymphocytic/granulocytic infiltrate
• however, pre-lesion mouse skin is normal


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
04/09/2024
MGI 6.23
The Jackson Laboratory