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Human Disease and Mouse Model Detail
Human Disease Waardenburg Syndrome, Type 2E; WS2E
OMIM ID: 611584
Synonyms Hypogonadotropic Hypogonadism with Anosmia and Deafness, with or without Hypopigmentation; Waardenburg Syndrome; Waardenburg Syndrome, Type 2e, with or without Neurologic Involvement; Waardenburg Syndrome, Type IIE; Ws2e, with or without Neurologic Involvement
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
     Sox10 SOX10*   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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last database update
04/08/2014
MGI 5.17
The Jackson Laboratory