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Human Disease and Mouse Model Detail
Human Disease Gerstmann-Straussler Disease; GSD
OMIM ID: 137440
Human Phenotype Ontology associations
Synonyms Amyloidosis, Cerebral, with Spongiform Encephalopathy; Cerebellar Ataxia, Progressive Dementia, and Amyloid Deposits in Cns; Encephalopathy, Subacute Spongiform, Gerstmann-Straussler Type; Gerstmann-Straussler-Scheinker Disease; GSS
View all models View ALL (7) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     PRNP* Prnp* View 7 models HomoloGene and HGNC
Transgenes and
other genome features
Transgenes and other genome features developed in mice to model this disease.

     Transgenes and Other Genome Features Mouse Models
  Tg(Prnp*A116V*M128V)1309Jama View 1 model
  Tg(Prnp*P101L)174Sbp View 1 model
  Tg(Prnp*P101L)2247Sbp View 1 model
  Tg(Prnp*P101L)2862Sbp View 1 model
  Tg(Prnp*P101L)2866Sbp View 3 models
References Disease References using Mouse Models (4)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory