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Human Disease and Mouse Model Detail
Human Disease Mowat-Wilson Syndrome
OMIM ID: 235730
Synonyms Hirschsprung Disease-Mental Retardation Syndrome; Microcephaly, Mental Retardation, and Distinct Facial Features, with or without Hirschsprung Disease
View all models View ALL (1) 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
     Zeb2* ZEB2* View 1 model 1:1 Homology
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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Funding Information
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Send questions and comments to User Support. 		last database update
05/22/2013
MGI 5.13 		The Jackson Laboratory