				Excel File Text File All mouse models of variable age at onset electroclinical syndrome with phenotypic similarity to the human disease
				Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
				progressive myoclonus epilepsy 1B	Prickle1em1Yzou/Prickle1+	C57BL/6-Prickle1^em1Yzou	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
				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	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