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All mouse models of movement disease with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | episodic kinesigenic dyskinesia 1 | Prrt2tm1d(KOMP)Wtsi/Prrt2+ | B6(Cg)-Prrt2tm1d(KOMP)Wtsi | J:299667 | View | |||
| episodic kinesigenic dyskinesia 1 | Prrt2tm1d(KOMP)Wtsi/Prrt2tm1d(KOMP)Wtsi | B6(Cg)-Prrt2tm1d(KOMP)Wtsi | J:299667 | View | ||||
| myoclonic dystonia 11 | Sgcetm1Ygl/Sgce+ | involves: 129S2/SvPas | J:180682 | View | ||||
| myoclonic dystonia 11 | Sgcetm1Ygl/Sgcetm1Ygl | involves: 129S2/SvPas * 129S4/SvJaeSor * BALB/c * C57BL/6 | J:101332 | View | ||||
| neurodevelopmental disorder with involuntary movements | Gnao1em2Rneu/Gnao1+ | C57BL/6J-Gnao1em2Rneu | J:303229 | View | ||||
| paroxysmal nonkinesigenic dyskinesia 1 | Tg(Pnkd*A7V*A9V,-DsRed)671Ljp/0 | B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)671Ljp | J:192798 | View | ||||
| paroxysmal nonkinesigenic dyskinesia 1 | Tg(Pnkd*A7V*A9V,-DsRed)704Ljp/0 | B6.Cg-Tg(Pnkd*A7V*A9V,-DsRed)704Ljp | J:192798 | View | ||||
| torsion dystonia 1 | Tor1atm1Wtd/Tor1a+ | B6;129-Tor1atm1Wtd/J | J:225496 | View | ||||
| torsion dystonia 1 | Tor1atm1Yql/Tor1a+ | involves: 129S2/SvPas * C57BL/6 | J:104513 | View | ||||
| torsion dystonia 1 | Tor1atm2Wtd/Tor1a+ | B6.129S1-Tor1atm2Wtd | J:171370, J:201962 | View | ||||
| torsion dystonia 1 | Tor1atm2Wtd/Tor1a+ | involves: 129S1/Sv | J:201535 | View | ||||
| torsion dystonia 6 | Thap1tm1.1Meeh/Thap1+ | involves: 129S/SvEv * C3H * C57BL/6 | J:226849 | View | ||||
| torsion dystonia 6 | Thap1tm1.2Meeh/Thap1+ | involves: 129S/SvEv * BALB/cJ * C3H * C57BL/6 | J:226849 | View | ||||
| | focal dystonia | Tor1atm1Calak/Tor1atm1Calak | involves: 129 * C57BL/6 | J:247570 | View | |||
| generalized dystonia | Cacna1atg/Cacna1atg | B6.D2-Cacna1atg/J | J:233263 | View | ||||
| generalized dystonia | Cacna1atg/Cacna1atm2.1Maag | involves: 129P2/OlaHsd * C57BL/6J * DBA/2J * FVB/N | J:233263 | View | ||||
| movement disease | Efnb3m1Btlr/Efnb3m1Btlr | involves: C57BL/6J | J:194586 | View | ||||
| Stiff-Person syndrome | Trak1hyrt/Trak1hyrt | involves: AKR * C3HeB/FeJ * C57BL/6J | J:105231 | View | ||||
| Transgenes and Other Mutations | torsion dystonia 1 | Tg(CMV-TOR1A*)1Nush/0 | involves: C3H * C57BL/6 | J:98716 | View | |||
| torsion dystonia 1 | Tg(CMV-TOR1A*)2Nush/0 | involves: C3H * C57BL/6 | J:98716 | View | ||||
| torsion dystonia 1 | Tg(Eno2-TOR1A*)13Shas/0 | involves: C3H * C57BL/6J | J:95447 | View | ||||
| Additional Complex Models | dystonia |
Ptstm1Ich/Ptstm1Ich Tg(DBH-PTS)6Csic/0 |
B6.Cg-Ptstm1Ich Tg(DBH-PTS)6Csic | J:102278 | View | |||
| dystonia |
Ptstm1Ich/Ptstm1Ich Tg(DBH-PTS)6Csic/0 |
involves: 129X1/SvJ * C57BL/6J | J:138968 | View | ||||
| essential tremor |
Cacna1gtm1Hssh/Cacna1gtm1Hssh Gabra1tm1.1Geh/Gabra1tm1.1Geh |
involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J | J:174980 | 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 | Stiff-Person syndrome | Gad2tm1Bae/Gad2tm1Bae | involves: 129X1/SvJ * C57BL/6 | J:44638 | View | |||
| Stiff-Person syndrome | Gad2tm1Bae/Gad2tm1Bae | involves: 129X1/SvJ * NOD | J:44638 | View | ||||