Excel File Text File All mouse models of spinocerebellar ataxia 17 with phenotypic similarity to the human disease
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
      spinocerebellar ataxia 17 Tbptm1Xjl/Tbp+
Tg(CAG-cre/Esr1*)5Amc/0
involves: 129S/SvEv * C57BL/6 * CBA J:213011 View
Transgenes and
Other Mutations
     spinocerebellar ataxia 17 Tg(Pcp2-TBP*)69Hmhl/0 involves: FVB/N J:174239 View
spinocerebellar ataxia 17 Tg(Prnp-TBP*)71-16Xjl/0 FVB/N-Tg(Prnp-TBP*)71-16Xjl J:130775 View
spinocerebellar ataxia 17 Tg(Prnp-TBP*)71-27Xjl/0 FVB/N-Tg(Prnp-TBP*)71-27Xjl J:130775 View
spinocerebellar ataxia 17 Tg(Prnp-TBP*)105Xjl/0 FVB/N-Tg(Prnp-TBP*)105Xjl J:130775 View


       
No similarity to the expected human disease phenotype was found.
        Disease Term Allelic Composition Genetic Background Reference Phenotypes
NOT Models      spinocerebellar ataxia 17 Tg(Prnp-TBP*)13Xjl/0 FVB/N-Tg(Prnp-TBP*)13Xjl J:130775 View