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Human Disease and Mouse Model Detail
Human Disease Koolen-De Vries Syndrome; KDVS
OMIM ID: 610443
Synonyms Chromosome 17q21.31 Deletion Syndrome; Mental Retardation, Autosomal Dominant; Microdeletion 17q21.31 Syndrome
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
     Kansl1 KANSL1*   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
07/23/2014
MGI 5.19
The Jackson Laboratory