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All mouse models of heart conduction disease with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | Brugada syndrome 1 | Scn5atm1Agrc/Scn5a+ | involves: 129 | J:166438 | View | |||
| Brugada syndrome 1 | Scn5atm1Care/Scn5a+ | FVB.129P2-Scn5atm1Care/Care | J:128657 | View | ||||
| Brugada syndrome 7 | Scn3btm1Clhh/Scn3btm1Clhh | 129S/SvEv-Scn3btm1Clhh | J:177262 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1.1Clhh/Ryr2tm1.1Clhh | 129S/SvEv-Ryr2tm1.1Clhh | J:186379 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1.1Maya/Ryr2+ | C57BL/6J-Ryr2tm1.1Maya | J:159451 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1Sgp/Ryr2+ | involves: 129/Sv * C57BL/6 | J:109683 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1Slh/Ryr2+ | involves: 129S7/SvEvBrd * C57BL/6 | J:111780 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm1Slh/Ryr2+ | involves: 129S7/SvEvBrd * C57BL/6J | J:235432 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm2Amks/Ryr2+ | involves: 129S1/Sv * 129X1/SvJ | J:212640 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm2Hhv/Ryr2+ | involves: 129 * C57BL/6 | J:212870 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm3.1Amks/Ryr2+ | involves: C57BL/6 | J:212640 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm3.1Hhv/Ryr2+ | involves: 129S7/SvEvBrd * C57BL/6 | J:220671 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 1 | Ryr2tm4.1Amks/Ryr2+ | involves: 129 * C57BL/6 | J:212640 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm1.1Sgp/Casq2tm1.1Sgp | involves: 129X1/SvJ * C57BL/6NCrL | J:151367 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm1Jse/Casq2tm1Jse | involves: FVB/N | J:124211 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm1Kpfe/Casq2tm1Kpfe | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:114621 | View | ||||
| catecholaminergic polymorphic ventricular tachycardia 2 | Casq2tm2Jse/Casq2tm2Jse | Not Specified | J:124211 | View | ||||
| progressive familial heart block type IA | Scn5atm1Agrc/Scn5a+ | involves: 129 | J:109689 | View | ||||
| progressive familial heart block type IA | Scn5atm1Agrc/Scn5a+ | involves: 129 * C57BL/6J | J:76331 | View | ||||
| short QT syndrome | Kcnh2tm1Hjd/Kcnh2tm1Hjd | involves: 129S1/Sv * 129X1/SvJ * C57BL/6 | J:82249 | View | ||||
| sick sinus syndrome | Scn5aem1Coop/Scn5a+ | involves: FVB/NJ | J:279087 | View | ||||
| sick sinus syndrome | Scn5aem1Coop/Scn5aem1Coop | involves: C57BL/6NJ * FVB/NJ | J:279087 | View | ||||
| | atrial fibrillation | Rbm20em1Hide/Rbm20em1Hide | involves: C57BL/6J | J:297234 | View | |||
| catecholaminergic polymorphic ventricular tachycardia | Fkbp1btm1Amks/Fkbp1btm1Amks | DBA/1LacJ-Fkbp1btm1Amks | J:107733 | View | ||||
| heart conduction disease | Slc6a2tm1.1Mkh/Slc6a2+ | B6.129S6-Slc6a2tm1.1Mkh | J:200046 | View | ||||
| sick sinus syndrome | Hcn1tm2Kndl/Hcn1tm2Kndl | involves: 129 * 129S/SvEv * C57BL/6J * C57BL/6N | J:219164 | View | ||||
| sinoatrial node disease | Ank2tm1Bnt/Ank2+ | involves: 129 | J:163867 | View | ||||
| Wolff-Parkinson-White syndrome |
Bmpr1atm1Bhr/Bmpr1atm2.1Bhr Tg(GATA6-cre)#Jbeb/0 |
involves: 129S7/SvEvBrd * C57BL/6 * FVB | J:111392 | View | ||||
| Wolff-Parkinson-White syndrome |
Tg(CAG-Map3k7*K63W)1232Mds/0 Tg(Myh6-cre)2182Mds/0 |
involves: FVB/N | J:117108 | View | ||||
| | sick sinus syndrome |
Gt(ROSA)26Sortm1(DTA)Jpmb/Gt(ROSA)26Sor+ Hcn4tm1(cre/ERT2)Anlu/Hcn4+ |
involves: 129S/SvEv | J:186021 | View | |||
| Transgenes and Other Mutations | familial atrial fibrillation |
Tg(Myh6-rtTA)8585Jam/0 Tg(Myh6*/tetO-SCN5A*F1759A)#Marx/0 |
involves: C57BL/6 * CBA * FVB/NTac | J:229825 | View | |||
| Wolff-Parkinson-White syndrome | Tg(Myh6-PRKAG2*R302Q)#Rro/0 | involves: FVB | J:108102 | View | ||||
| Wolff-Parkinson-White syndrome | Tg(Myh6-PRKAG2*R531G)22Dca/0 | involves: C57BL/10 * CBA/Ca | J:108517 | View | ||||