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All mouse models of focal epilepsy with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | autosomal dominant nocturnal frontal lobe epilepsy 3 | Chrnb2tm1.1Cont/Chrnb2tm1.1Cont | B6.129-Chrnb2tm1.1Cont | J:228269 | View | |||
| autosomal dominant nocturnal frontal lobe epilepsy 3 |
Tg(Prnp-tTA)F959Sbp/0 Tg(tetO-Chrnb2*V287L)H3Gica/0 |
involves: 129S7/SvEvBrd * FVB | J:145855 | View | ||||
| familial temporal lobe epilepsy 1 | Lgi1tm1.1Ics/Lgi1tm1.1Ics | involves: 129S2/SvPas * BALB/c * C57BL/6 | J:182795 | View | ||||
| familial temporal lobe epilepsy 1 |
Lgi1tm1.1Jkc/Lgi1tm1.1Jkc Tyrc-Brd/Tyrc-Brd |
B6.Cg-Tyrc-Brd Lgi1tm1.1Jkc | J:158715 | View | ||||
| familial temporal lobe epilepsy 1 | Lgi1tm1Mafu/Lgi1tm1Mafu | involves: 129S6/SvEvTac * C57BL/6 | J:157578 | View | ||||
| familial temporal lobe epilepsy 1 | Tg(Lgi1*)#Mpan/0 | Not Specified | J:154129 | View | ||||
| | temporal lobe epilepsy |
Glultm1.1Ncd/Glultm1.1Ncd Emx1tm1(cre)Krj/Emx1+ |
B6.Cg-Glultm1.1Ncd Emx1tm1(cre)Krj | J:272643 | View | |||
| temporal lobe epilepsy | Kcna1tm1Tem/Kcna1tm1Tem | C3Fe.129S7-Kcna1tm1Tem | J:206598 | View | ||||
| temporal lobe epilepsy | Slc32a1tm2(cre)Lowl/Slc32a1tm2(cre)Lowl | either: B6J.129S6(FVB)-Slc32a1tm2(cre)Lowl or (involves: 129S6/SvEvTac * C57BL/6J * FVB/N) | J:308516 | 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 | autosomal dominant nocturnal frontal lobe epilepsy 1 | Chrna4tm1Dra/Chrna4tm1Dra | involves: 129S4/SvJae * C57BL/6 | J:64208, J:97020 | View | |||