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| 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 | ||||
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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 17 | Tg(Prnp-TBP*)13Xjl/0 | FVB/N-Tg(Prnp-TBP*)13Xjl | J:130775 | View | |||