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Human Disease and Mouse Model Detail
Human Disease Ritscher-Schinzel Syndrome; RTSC
OMIM ID: 220210
Synonyms 3C Syndrome; Craniocerebellocardiac Dysplasia; Dandy-Walker-Like Malformation with Atrioventricular Septal Defect
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
     E430025E21Rik KIAA0196*   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
07/15/2014
MGI 5.18
The Jackson Laboratory