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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
| spinocerebellar ataxia 5 | Sptbn2Gt(XK442)Byg/Sptbn2Gt(XK442)Byg | involves: 129P2/OlaHsd * C57BL/6J | J:158494 | View | |||
| spinocerebellar ataxia 5 | Sptbn2tm1Mjac/Sptbn2tm1Mjac | B6.129P2-Sptbn2tm1Mjac | J:159622 | View | ||||
| Transgenes and Other Mutations | spinocerebellar ataxia 5 |
Tg(Pcp2-tTA)3Horr/0 Tg(tetO-SPTBN2*)#Lpwr/0 |
involves: FVB/N | J:215593 | 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 5 | Sptbn2tm1Mjac/Sptbn2+ | involves: 129P2/OlaHsd | J:163169 | View | |||