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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Prnp*)#Rgab
transgene insertion, Ruth Gabizon
MGI:5428331
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Prnptm1Cwe/Prnptm1Cwe
Tg(Prnp*)#Rgab/0
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N MGI:5428333
tg2
Tg(Prnp*)#Rgab/0 involves: C57BL/6 * FVB/N MGI:5428334


Genotype
MGI:5428333
cx1
Allelic
Composition
Prnptm1Cwe/Prnptm1Cwe
Tg(Prnp*)#Rgab/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Prnptm1Cwe mutation (29 available); any Prnp mutation (88 available)
Tg(Prnp*)#Rgab mutation (0 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are euthanized when they are too paralyzed to reach food and water

behavior/neurological
• in very few mice
• asymmetric hindlimb weakness at 5 to 6 months that progresses to paraplegia
• asymmetric hindlimb weakness at 5 to 6 months that progresses to paraplegia
• myoclonic jerks in some mice

limbs/digits/tail
• plastic tail in very few mice

muscle
• myoclonic jerks in some mice
• in the lower body

nervous system
• myoclonic jerks in some mice
• at 3 months and more prominent at 8 months
• at 3 months and more prominent at 8 months

skeleton

Mouse Models of Human Disease
OMIM ID Ref(s)
Creutzfeldt-Jakob Disease; CJD 123400 J:183170




Genotype
MGI:5428334
tg2
Allelic
Composition
Tg(Prnp*)#Rgab/0
Genetic
Background
involves: C57BL/6 * FVB/N
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• mice are euthanized when they are too paralyzed to reach food and water

behavior/neurological
• in very few mice
• asymmetric hindlimb weakness at 5 to 6 months that progresses to paraplegia
• asymmetric hindlimb weakness at 5 to 6 months that progresses to paraplegia
• myoclonic jerks in some mice

limbs/digits/tail
• plastic tail in very few mice

muscle
• myoclonic jerks in some mice
• in the lower body

nervous system
• myoclonic jerks in some mice
• at 3 months and more prominent at 8 months
• at 3 months and more prominent at 8 months

skeleton

Mouse Models of Human Disease
OMIM ID Ref(s)
Creutzfeldt-Jakob Disease; CJD 123400 J:183170





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last database update
06/22/2016
MGI 6.04
The Jackson Laboratory