| Human Disease |
Alagille Syndrome 1; ALGS1 OMIM ID: 118450 |
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| Synonyms | Alagille Syndrome; ALGS; Alagille-Watson Syndrome; AWS; Arteriohepatic Dysplasia; AHD; Cholestasis with Peripheral Pulmonary Stenosis; Hepatic Ductular Hypoplasia, Syndromatic | |||||||||||||||||||||
| View all models | View ALL (5) mouse models for this human disease. | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Jag1tm1Frad/Jag1tm1Frad Tg(Tagln-cre)1Her/0 |
B6.Cg-Jag1tm1Frad Tg(Tagln-cre)1Her | J:166890 | View |
| Jag1Mhdahtu/Jag1+ |
C3HeB/FeJ-Jag1Mhdahtu | J:72108 | View |
| Jag1tm1Frad/Jag1tm1Frad Tg(Cdh5-cre)7Mlia/0 |
B6.Cg-Jag1tm1Frad Tg(Cdh5-cre)7Mlia | J:189213 | View |
| Jag1tm1Grid/Jag1+ Notch2tm1Grid/Notch2+ |
involves: 129S1/Sv * C57BL/6J | J:74574 | View |
| Jag1tm2Grid/Jag1tm2Grid Tg(Wnt1-cre)11Rth/0 |
involves: 129S1/Sv * C57BL/6 * CBA | J:181120 | View |
| Allelic Composition | Genetic Background | Reference | Phenotypes |
| Jag1tm1Grid/Jag1+ |
involves: 129S1/Sv * C57BL/6 * FVB | J:54907 | View |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 05/22/2013 MGI 5.13 |
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