Phenotypes associated with this allele
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Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prnptm2(PRNP*129M)Tkit mutation
(0 available);
any
Prnp mutation
(150 available)
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immune system
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• one mouse was are weakly susceptible while others are not susceptible to bovine spongiform encephalopathy prion infection
(J:105882)
• mice are less susceptible to infection with non-plaque-type dura matter graft-associated Creutzfeldt-Jakob and sporadic Creutzfeldt-Jakob VV2 than Prnptm3(PRNP*129V)Tkit homozygotes
(J:126777)
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• mice are highly susceptible to variant Creutzfeldt-Jakob prion infection
(J:105882)
• incubation period following infection with sporadic Creutzfeldt-Jakob MM1 prion infection is 467+/-24 days compared to 542 and 648 days for 2 Prnptm3(PRNP*129V)Tkit homozygous mice
(J:126777)
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|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prnptm2(PRNP*129M)Tkit mutation
(0 available);
any
Prnp mutation
(150 available)
Prnptm3(PRNP*129V)Tkit mutation
(0 available);
any
Prnp mutation
(150 available)
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|
|
immune system
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• mice are weakly susceptible to variant Creutzfeldt-Jakob prion infection
|
|
Find Mice |
Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prnptm2(PRNP*129M)Tkit mutation
(0 available);
any
Prnp mutation
(150 available)
Tg(Prnp-PRNP*129M)1Tkit mutation
(0 available)
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immune system
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• incubation period following infection with sporadic Creutzfeldt-Jakob VV2 prions is 723+/-79 days compared to 312+/-7 days for Prnptm3(PRNP*129V)Tkit homozygous mice
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• incubation period following infection with sporadic Creutzfeldt-Jakob MM1 prions is 429+/-6 days compared to 542 and 648 days for 2 Prnptm3(PRNP*129V)Tkit homozygous mice
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nervous system
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• following infection with sporadic Creutzfeldt-Jakob MM1 prion, mice exhibit diffuse synaptic-type prion protein deposits
• following infection with sporadic Creutzfeldt-Jakob VV2 prion, mice exhibit more prominent plaque-type prion protein deposits with larger plaque-type deposits spread throughout the cerebral gray matter and thalamus rather than the white matter
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