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Human Disease and Mouse Model Detail
Human Disease Meckel Syndrome, Type 1; MKS1
OMIM ID: 249000
Synonyms Dysencephalia Splanchnocystica; Gruber Syndrome; Meckel Syndrome; Meckel Syndrome; MKS; Meckel-Gruber Syndrome; Meckel-Gruber Syndrome, Type 1; MES
View all models View ALL (3) mouse models for this human disease.
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
     Mks1* MKS1* View 3 models 1:1 Homology
References Disease References using Mouse Models (3)

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
09/02/2014
MGI 5.19
The Jackson Laboratory