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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

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     SOX10* Sox10   HomoloGene and HGNC

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
MGI 6.04
The Jackson Laboratory