- reduced long term potentiation / MGI
- abnormal CNS synaptic transmission / MGI
- abnormal inhibitory postsynaptic potential / MGI
- abnormal inhibitory postsynaptic currents / MGI
- behavior/neurological phenotype / MGI
- decreased brain copper level / MGI
- tremors / MGI
- abnormal cerebellum morphology / MGI
- decreased Purkinje cell number / MGI
STOCK Prnptm1Cwe Tg(Prnp/PRNP*ARR)FM16Pcg/H
Status | Available to order |
EMMA ID | EM:04338 |
International strain name | STOCK Prnptm1Cwe Tg(Prnp/PRNP*ARR)FM16Pcg/H |
Alternative name | Tg(OvPrP)FM16 |
Strain type | Targeted Mutant Strains : Knock-out |
Allele/Transgene symbol | Prnptm1Cwe, |
Gene/Transgene symbol | Prnp |
Information from provider
Provider | Peter Griffiths |
Provider affiliation | Department of Pathology and Host Susceptibility, Animal Health and Veterinary Laboratories Agency (AHVLA) |
Genetic information | A ~12 kb transgene, comprised of chimaeric DNA sequence encoding a sheep PrP (ARR allele) coding region and mouse PrP gene promoter and 3'-UTR, was used to microinject pronuclear stage FVB/N fertilised oocytes. |
Phenotypic information | Overexpression of transgenic ovine PrPC in brain and other tissues in order to confer increased susceptibility to TSE diseases compared to wild-type mice. |
Breeding history | Bred to 9 generations by crossing with PrP null (Zurich I) mice. Maintained as a transgene heterozygous line. |
References | None available |
Homozygous fertile | not known |
Homozygous viable | not known |
Homozygous matings required | no |
Immunocompromised | not known |
Information from EMMA
Archiving centre | Mary Lyon Centre at MRC Harwell, Oxford, United Kingdom |
Animals used for archiving | heterozygous 0, heterozygous 0 |
Breeding at archiving centre | No breeding was performed at the archiving centre. |
Stage of embryos | 8-cell |
Disease and phenotype information
Orphanet associated rare diseases, based on orthologous gene matching
- Inherited Creutzfeldt-Jakob disease / Orphanet_282166
- Familial Alzheimer-like prion disease / Orphanet_280397
- Huntington disease-like 1 / Orphanet_157941
- PrP systemic amyloidosis / Orphanet_397606
- Fatal familial insomnia / Orphanet_466
- Gerstmann-Straussler-Scheinker syndrome / Orphanet_356
- Sporadic fatal insomnia / Orphanet_586130
MGI phenotypes (allele matching)
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