	Excel File Text File All mouse models of electroclinical syndrome with phenotypic similarity to the human disease
	Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
	benign neonatal seizures	Kcnq2tm1.1Naas/Kcnq2+	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	J:154582	View
	benign neonatal seizures	Kcnq2tm1.1Naas/Kcnq2tm1.1Naas	B6.129-Kcnq2^tm1.1Naas	J:154582	View
	benign neonatal seizures	Kcnq2tm1.1Naas/Kcnq2tm1.1Naas	FVB.129-Kcnq2^tm1.1Naas	J:154582	View
	benign neonatal seizures	Kcnq2tm1.1Naas/Kcnq2tm1.1Naas	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	J:154582	View
	benign neonatal seizures	Kcnq2tm1Hsa/Kcnq2+	involves: 129P2/OlaHsd * C57BL/6	J:62797	View
	benign neonatal seizures	Kcnq3tm1.1Naas/Kcnq3+	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	J:154582	View
	benign neonatal seizures	Kcnq3tm1.1Naas/Kcnq3+	involves: 129S1/Sv * 129X1/SvJ * FVB/N	J:154582	View
	benign neonatal seizures	Kcnq3tm1.1Naas/Kcnq3tm1.1Naas	B6.129-Kcnq3^tm1.1Naas	J:154582	View
	benign neonatal seizures	Kcnq3tm1.1Naas/Kcnq3tm1.1Naas	FVB.129-Kcnq3^tm1.1Naas	J:154582	View
	benign neonatal seizures	Kcnq3tm1.1Naas/Kcnq3tm1.1Naas	involves: 129S1/Sv * 129X1/SvJ * C57BL/6	J:154582	View
	developmental and epileptic encephalopathy 2	Cdkl5tm1.2Cogr/Cdkl5tm1.2Cogr	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	J:209635	View
	developmental and epileptic encephalopathy 2	Cdkl5tm1.2Cogr/Y	involves: 129P2/OlaHsd * 129S1/Sv * 129S4/SvJaeSor * C57BL/6J	J:209635	View
	developmental and epileptic encephalopathy 7	Kcnq2tm1.1Lvi/Kcnq2+	129-Kcnq2^tm1.1Lvi/Lvi	J:298666	View
	developmental and epileptic encephalopathy 14	Kcnt1em1Lekk/Kcnt1+	C57BL/6J-Kcnt1^em1Lekk	J:287751	View
	developmental and epileptic encephalopathy 14	Kcnt1em1Pqt/Kcnt1em1Pqt	C57BL/6J-Kcnt1^em1Pqt	J:333512	View
	developmental and epileptic encephalopathy 16	Tbc1d24em2Tbf/Tbc1d24em2Tbf	C57BL/6J-Tbc1d24^em2Tbf	J:273646	View
	developmental and epileptic encephalopathy 17	Gnao1em1Rneu/Gnao1+	involves: C57BL/6J * C57BL/6NCrl	J:271137	View
	developmental and epileptic encephalopathy 17	Gnao1tm2.1Rneu/Gnao1+	B6.129S-Gnao1^tm2.1Rneu	J:216850	View
	developmental and epileptic encephalopathy 17	Gnao1tm2Rneu/Gnao1+	B6.129S1-Gnao1^tm2Rneu	J:271137	View
	developmental and epileptic encephalopathy 39	Slc25a12Gt(OST123999)Lex/Slc25a12Gt(OST123999)Lex	involves: 129S5/SvEvBrd * C57BL/6	J:243212	View
	developmental and epileptic encephalopathy 54	Hnrnpuem1Frk/Hnrnpu+	Not Specified	J:342579	View
	Dravet syndrome	Scn1atm1.1Kzy/Scn1a+	involves: 129P2/OlaHsd * C3HeB/FeJ	J:260796	View
	Dravet syndrome	Scn1atm1Kea/Scn1a+	(C57BL/6J x 129S6/SvEvTac-Scn1a^tm1Kea)F1	J:203040	View
	Dravet syndrome	Scn1atm1Wac/Scn1a+	B6.129-Scn1a^tm1Wac	J:113149, J:188126	View
	Dravet syndrome	Scn1atm1Wac/Scn1a+	involves: 129S1/Sv * 129X1/SvJ * FVB/NJ	J:129998	View
	Dravet syndrome	Scn1atm2.1Kzy/Scn1a+ Tg(Pvalb-cre)1Tama/0	involves: 129P2/OlaHsd * C57BL/6 * DBA	J:202863	View
	Dravet syndrome	Scn1atm2.1Kzy/Scn1atm2.1Kzy Tg(Pvalb-cre)1Tama/0	involves: 129P2/OlaHsd * C57BL/6 * DBA	J:202863	View
	Dravet syndrome	Scn1atm2.1Wac/Scn1a+ Tg(I12b-cre)1Jlr/0	involves: 129X1/SvJ * C57BL/6J	J:188126	View
	Dravet syndrome	Scn1atm2.1Wac/Scn1a+ Tg(I12b-cre)1Jlr/0	involves: C57BL/6J * CD-1	J:189897	View
	juvenile myoclonic epilepsy	Efhc1tm1Kzy/Efhc1+	B6.129P2-Efhc1^tm1Kzy	J:145858	View
	juvenile myoclonic epilepsy	Efhc1tm1Kzy/Efhc1tm1Kzy	B6.129P2-Efhc1^tm1Kzy	J:145858	View
	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
	childhood electroclinical syndrome	Cacna1atg/Cacna1atg	B6.D2-Cacna1a^tg/J	J:6154	View
	early infantile epileptic encephalopathy	Arxtm1.1Ics/Y	involves: 129S2/SvPas * C57BL/6J * C57BL/6N	J:262482	View
	early infantile epileptic encephalopathy	Arxtm1.1Jno/Y	involves: 129S7/SvEvBrd * C57BL/6J	J:151082	View
	early infantile epileptic encephalopathy	Arxtm1Gldn/Arx+ Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	J:148311	View
	early infantile epileptic encephalopathy	Arxtm1Gldn/Y Tg(mI56i-cre,EGFP)1Kc/0	involves: 129/Sv * C57BL/6 * CD-1 * FVB/N	J:148311	View
	early infantile epileptic encephalopathy	Arxtm4Kki/Y	involves: 129S/SvEv * C57BL/6J	J:197588	View
	early infantile epileptic encephalopathy	Arxtm4Kki/Y	involves: 129S/SvEv * C57BL/6NHsd	J:260340	View
	early infantile epileptic encephalopathy	Arxtm5Kki/Y	involves: 129S/SvEv * C57BL/6NHsd	J:260340	View
	early infantile epileptic encephalopathy	Got2em2Pcamp/Got2em2Pcamp	involves: C57BL/6	J:291216	View
	early infantile epileptic encephalopathy	Got2em3Pcamp/Got2em3Pcamp	involves: C57BL/6	J:291216	View
	early infantile epileptic encephalopathy	Scn8aem1Mm/Scn8a+	involves: C57BL/6J * SJL	J:207931	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
	Lennox-Gastaut syndrome	DgkdGt(RRT600)Byg/DgkdGt(RRT600)Byg	involves: 129P2/OlaHsd * C57BL/6	J:126380	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

	No similarity to the expected human disease phenotype was found.
	Disease Term	Allelic Composition	Genetic Background	Reference	Phenotypes
NOT Models	developmental and epileptic encephalopathy	Pigkem1Linwu/Pigkem1Linwu	involves: C57BL/6J	J:305399	View
	developmental and epileptic encephalopathy	Pigkem2Linwu/Pigkem2Linwu	involves: C57BL/6J	J:305399	View
	developmental and epileptic encephalopathy 14	Kcnt1em1Pqt/Kcnt1+	C57BL/6J-Kcnt1^em1Pqt	J:333512	View