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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Pcdh17tm1.1Sia
targeted mutation 1.1, Shinichi Aizawa
MGI:5520081
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Pcdh17tm1.1Sia/Pcdh17tm1.1Sia involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj MGI:5520082


Genotype
MGI:5520082
hm1
Allelic
Composition
Pcdh17tm1.1Sia/Pcdh17tm1.1Sia
Genetic
Background
involves: C57BL/6 * C57BL/6NCrlj * CBA/JNCrlj
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pcdh17tm1.1Sia mutation (0 available); any Pcdh17 mutation (53 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• mice exhibit normal corticobasal ganglia circuitry
• mice exhibit normal average postsynaptic spine area, PSD length, synaptic cleft width and density of asymmetric synapses
• mice exhibit normal basic properties of AMPA and NMDA receptors at corticostriatal synapses and synaptic transmission
• increased number of docked synaptic vesicles and total number of synaptic vesicles per presynaptic terminal in the inner, but not outer, lateral globus pallidus
• weaker depression of normalized excitatory postsynaptic current amplitude
• weaker synaptic depression following repetitive stimulation
• increased paired-pulse ratio of inhibitory postsynaptic currents

behavior/neurological
N
• mice exhibit normal spontaneous locomotor activity, anxiety-related behavior, fear learning, startle response and pain behavior
• mice spend less time immobile in a tail suspension test and forced swim test





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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
11/12/2024
MGI 6.24
The Jackson Laboratory