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All mouse models of X-linked hereditary ataxia with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | fragile X-associated tremor/ataxia syndrome | Fmr1tm2Cgr/Y | involves: 129P2/OlaHsd * C57BL/6J * FVB | J:104445 | View | |||
| Transgenes and Other Mutations | fragile X-associated tremor/ataxia syndrome |
Tg(Hnrnpa2b1-rtTA2S*M2)9Jstr/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0 |
involves: C57BL/6JRj * FVB/N | J:229379 | View | |||
| fragile X-associated tremor/ataxia syndrome | Tg(Pcp2-FMR1*)1Dln/0 | C57BL/6-Tg(Pcp2-Fmr1*)1Dln | J:149320 | View | ||||
| fragile X-associated tremor/ataxia syndrome |
Tg(Prnp-rtTA2S*M2)#Rkhu/0 Tg(tetO-FMR1*,-EGFP)#Rkhu/0 |
involves: C57BL/6JRj | J:224760 | View | ||||