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All mouse models of spinocerebellar ataxia type 17 with phenotypic similarity to the human disease
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
spinocerebellar ataxia type 17 |
Tbptm1Xjl/Tbp+ Tg(CAG-cre/Esr1*)5Amc/0 |
involves: 129S/SvEv * C57BL/6 * CBA | J:213011 | View | ||||
Transgenes and Other Mutations | spinocerebellar ataxia type 17 | Tg(Pcp2-TBP*)69Hmhl/0 | involves: FVB/N | J:174239 | View | |||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-16Xjl/0 | FVB/N-Tg(Prnp-TBP*)71-16Xjl | J:130775 | View | ||||
spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)71-27Xjl/0 | FVB/N-Tg(Prnp-TBP*)71-27Xjl | J:130775 | View | ||||
spinocerebellar ataxia type 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.
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Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
NOT Models | spinocerebellar ataxia type 17 | Tg(Prnp-TBP*)13Xjl/0 | FVB/N-Tg(Prnp-TBP*)13Xjl | J:130775 | View |