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Human Disease and Mouse Model Detail
Human Disease Galloway-Mowat Syndrome; GAMOS
OMIM ID: 251300
Human Phenotype Ontology associations
Synonyms Cerebellar Ataxia with Mental Retardation, Optic Atrophy, and Skin Abnormalities; CAMOS; Galloway Syndrome; Microcephaly, Hiatal Hernia, and Nephrotic Syndrome; Nephrosis-Microcephaly Syndrome; Nephrosis-Neuronal Dysmigration Syndrome; Spinocerebellar Ataxia, Autosomal Recessive 5, Formerly; SCAR5, FORMERLY
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
     WDR73* Wdr73   HomoloGene and HGNC
ZNF592* Zfp592   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 6.07
The Jackson Laboratory