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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Pcp2-cre)1Amc
transgene insertion 1, Andrew P McMahon
MGI:3656031
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cn1
Shhtm2Amc/Shhtm3Amc
Tg(Pcp2-cre)1Amc/0
involves: 129S1/Sv * 129X1/SvJ * Black Swiss MGI:3656218
cn2
Cdk5r1tm2Ohsh/Cdk5r1tm2Ohsh
Tg(Pcp2-cre)1Amc/0
involves: C57BL/6 * C57BL/6N MGI:5824372


Genotype
MGI:3656218
cn1
Allelic
Composition
Shhtm2Amc/Shhtm3Amc
Tg(Pcp2-cre)1Amc/0
Genetic
Background
involves: 129S1/Sv * 129X1/SvJ * Black Swiss
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Shhtm2Amc mutation (1 available); any Shh mutation (45 available)
Shhtm3Amc mutation (0 available); any Shh mutation (45 available)
Tg(Pcp2-cre)1Amc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• pups display movement disorders characteristic of abnormal cerebellar function

nervous system
• at E18.5, cerebellum is detected to be abnormal with immature fissures and a reduction in the external granule layer; however no difference in cerebellar volume is evident between mutants and wild-type
• at E18.5 mutants have 5 rudimentary lobules
• at P5, cerebellum has small primitive lobules
• at P5 cells are dispersed in a thinner layer than in control Shhtm2Amc/Shhtm3Amc control mice or Shhtm2Amc/Shhtm3Amc;Tg(Pax2-cre)1Amc mice
• dendrite projections of cells are hard to distinguish
• at P14, there is a layer of Purkinje neurons that is better organized than in Shhtm2Amc/Shhtm3Amc;Tg(Pax2-cre)1Amc mice
• at P5 number is reduced by 20% compared to controls
• in adults, a 35% reduction is apparent
• in adults, cerebellum is small but has distinct lobes with Purkinje cells organized into a 1-2 cell layer overlayed by a thin inner germinal layer




Genotype
MGI:5824372
cn2
Allelic
Composition
Cdk5r1tm2Ohsh/Cdk5r1tm2Ohsh
Tg(Pcp2-cre)1Amc/0
Genetic
Background
involves: C57BL/6 * C57BL/6N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdk5r1tm2Ohsh mutation (0 available); any Cdk5r1 mutation (13 available)
Tg(Pcp2-cre)1Amc mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• mice show a significantly impaired ability to maintain balance on a rotating rod at 3 different speeds (16, 24 and 32 rpm)
• in a balance beam test, mice show a significantly increased number of paw slips at two different beam diameters (11 mm and 28 mm)
• however, no gait disturbances are detected in a footprint test

nervous system
N
• cerebellar histology is grossly normal, with no significant alterations in Purkinje cell morphology in terms of alignment, density, axonal elongation or dendritic structure
• mice show impaired cerebellar long-term synaptic plasticity (LTD and LTP) at the parallel fiber (PF)-Purkinje cell synapse
• although Purkinje cells exhibit long-lasting potentiated PF-evoked excitatory post synaptic currents (EPSCs) after 300 PF-stimuli at 1 Hz, the amplitude of LTP is significantly smaller than that in control mice
• Purkinje cells fail to exhibit depressed PF-evoked EPSCs after conjunctive stimuli, unlike in control mice





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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory