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All mouse models of developmental and epileptic encephalopathy with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | 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 | ||||
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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 | ||||