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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-Kcnq2tm1.1Naas | J:154582 | View | ||||
benign neonatal seizures | Kcnq2tm1.1Naas/Kcnq2tm1.1Naas | FVB.129-Kcnq2tm1.1Naas | 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-Kcnq3tm1.1Naas | J:154582 | View | ||||
benign neonatal seizures | Kcnq3tm1.1Naas/Kcnq3tm1.1Naas | FVB.129-Kcnq3tm1.1Naas | 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-Kcnq2tm1.1Lvi/Lvi | J:298666 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Lekk/Kcnt1+ | C57BL/6J-Kcnt1em1Lekk | J:287751 | View | ||||
developmental and epileptic encephalopathy 14 | Kcnt1em1Pqt/Kcnt1em1Pqt | C57BL/6J-Kcnt1em1Pqt | J:333512 | View | ||||
developmental and epileptic encephalopathy 16 | Tbc1d24em2Tbf/Tbc1d24em2Tbf | C57BL/6J-Tbc1d24em2Tbf | 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-Gnao1tm2.1Rneu | J:216850 | View | ||||
developmental and epileptic encephalopathy 17 | Gnao1tm2Rneu/Gnao1+ | B6.129S1-Gnao1tm2Rneu | 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-Scn1atm1Kea)F1 | J:203040 | View | ||||
Dravet syndrome | Scn1atm1Wac/Scn1a+ | B6.129-Scn1atm1Wac | 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-Efhc1tm1Kzy | J:145858 | View | ||||
juvenile myoclonic epilepsy | Efhc1tm1Kzy/Efhc1tm1Kzy | B6.129P2-Efhc1tm1Kzy | J:145858 | 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 | ||||
![]() | childhood electroclinical syndrome | Cacna1atg/Cacna1atg | B6.D2-Cacna1atg/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.
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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-Kcnt1em1Pqt | J:333512 | View |