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Human Disease and Mouse Model Detail
Human Disease Alport Syndrome, Autosomal Recessive
OMIM ID: 203780
Synonyms Alport Syndrome
View all models View ALL (7) mouse models for this human disease.
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Gene is associated with the disease in this species
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Col4a3* COL4A3* View 5 models 1:1 Homology
Col4a4* COL4A4* View 1 model 1:1 Homology
     Mpv17* MPV17 View 1 model 1:1 Homology
References Disease References using Mouse Models (13)

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
11/18/2014
MGI 5.20
The Jackson Laboratory