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All mouse models of variable age at onset electroclinical syndrome with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | Lafora disease | Epm2atm1Kzy/Epm2atm1Kzy | involves: 129P2/OlaHsd * C57BL/6J | J:76688, J:173769 | View | |||
| Lafora disease | Nhlrc1tm1(KOMP)Vlcg/Nhlrc1tm1(KOMP)Vlcg | involves: C57BL/6J * C57BL/6NTac | J:165994, J:218959 | View | ||||
| Lafora disease | Nhlrc1tm1.2Geno/Nhlrc1tm1.2Geno | involves: 129S2/SvPas * C57BL/6J | J:181559 | View | ||||
| Lafora disease | Nhlrc1tm1Bmin/Nhlrc1tm1Bmin | involves: 129S6/SvEvTac * C57BL/6 * C57BL/6NCr | J:181674 | View | ||||
| progressive myoclonus epilepsy 1B | Prickle1em1Yzou/Prickle1+ | C57BL/6-Prickle1em1Yzou | J:321396 | View | ||||
| Unverricht-Lundborg syndrome | Cstbtm1Rm/Cstbtm1Rm | either: (involves: 129S1/Sv * 129X1/SvJ) or (involves: 129S1/Sv * 129X1/SvJ * C57BL/6) | J:50587, J:71823 | View | ||||
| | progressive myoclonus epilepsy | Scarb2tm1Psa/Scarb2tm1Psa | involves: 129P2/OlaHsd * C57BL/6N | J:216676 | View | |||
| Transgenes and Other Mutations | Lafora disease | Tg(CAG-EPM2A*C266S)1Bmin/0 | involves: 129 * C57BL/6 * SJL | J:262504, J:120356 | View | |||