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Human Disease and Mouse Model Detail
Human Disease Williams-Beuren Syndrome; WBS
OMIM ID: 194050
Synonyms Chromosome 7q11.23 Deletion Syndrome, 1.5- to 1.8-Mb; Williams Syndrome; WMS; WS
View all models View ALL (16) 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
     Baz1b* BAZ1B View 4 models 1:1 Homology
Clip2* CLIP2 View 1 model 1:1 Homology
Dlg4* DLG4 View 1 model 1:1 Homology
Eif4h* EIF4H View 1 model 1:1 Homology
Fzd9* FZD9 View 2 models 1:1 Homology
Gtf2i* GTF2I View 1 model 1:1 Homology
Gtf2ird1* GTF2IRD1 View 4 models 1:1 Homology
Limk1* LIMK1 View 1 model 1:1 Homology
     Eln ELN*   1:1 Homology
Mlxipl MLXIPL*   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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Send questions and comments to User Support. 		last database update
05/08/2013
MGI 5.13 		The Jackson Laboratory