About   Help   FAQ
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





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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
05/14/2024
MGI 6.23
The Jackson Laboratory