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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 (17) 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
     BAZ1B Baz1b* View 5 models HomoloGene and HGNC
CLIP2 Clip2* View 2 models HomoloGene and HGNC
DLG4 Dlg4* View 1 model HomoloGene and HGNC
EIF4H Eif4h* View 2 models HomoloGene and HGNC
FZD9 Fzd9* View 3 models HomoloGene and HGNC
GTF2I Gtf2i* View 3 models HomoloGene and HGNC
GTF2IRD1 Gtf2ird1* View 5 models HomoloGene and HGNC
LIMK1 Limk1* View 2 models HomoloGene
     ELN* Eln View 1 model HGNC
MLXIPL* Mlxipl View 1 model HomoloGene and HGNC
References Disease References using Mouse Models (15)

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
06/23/2015
MGI 5.22
The Jackson Laboratory