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Human Disease and Mouse Model Detail
Human Disease Meier-Gorlin Syndrome 1; MGORS1
OMIM ID: 224690
Human Phenotype Ontology associations
Synonyms Ear, Patella, Short Stature Syndrome; EPS; Meier-Gorlin Syndrome; Meier-Gorlin Syndrome; Microtia, Absent Patellae, Micrognathia Syndrome
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
     ORC1* Orc1   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