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Human Disease and Mouse Model Detail
Human Disease Alagille Syndrome 1; ALGS1
OMIM ID: 118450
Human Phenotype Ontology associations
Synonyms Alagille Syndrome; 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.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     JAG1* Jag1* View 5 models HomoloGene and HGNC
References Disease References using Mouse Models (6)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory