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All mouse models of Alagille syndrome with phenotypic similarity to the human disease
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| Disease Term | Allelic Composition | Genetic Background | Reference | Phenotypes | ||||
  | Alagille syndrome | Jag1Mhdahtu/Jag1+ | C3HeB/FeJ-Jag1Mhdahtu | J:72108 | View | |||
| Alagille syndrome | Jag1Ndr/Jag1Ndr | involves: C3HeB/FeJ * C57BL/6 | J:277897 | View | ||||
| Alagille syndrome |
Jag1tm1Frad/Jag1tm1Frad Tg(Cdh5-cre)7Mlia/0 |
B6.Cg-Jag1tm1Frad Tg(Cdh5-cre)7Mlia | J:189213 | View | ||||
| Alagille syndrome |
Jag1tm1Frad/Jag1tm1Frad Tg(Tagln-cre)1Her/0 |
B6.Cg-Jag1tm1Frad Tg(Tagln-cre)1Her | J:166890 | View | ||||
| Alagille syndrome |
Jag1tm1Grid/Jag1+ Notch2tm1Grid/Notch2+ |
involves: 129S1/Sv * C57BL/6J | J:74574 | View | ||||
| Alagille syndrome |
Jag1tm2Grid/Jag1tm2Grid H2az2Tg(Wnt1-cre)11Rth/H2az2+ |
involves: 129S1/Sv * C57BL/6 * CBA | J:181120 | 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 | Alagille syndrome | Jag1tm1Grid/Jag1+ | involves: 129S1/Sv * C57BL/6 * FVB | J:54907 | View | |||