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Human Disease and Mouse Model Detail
Human Disease Apert Syndrome
OMIM ID: 101200
Human Phenotype Ontology associations
Synonyms Acrocephalosyndactyly, Type I; ACS1
View all models View ALL (7) mouse models for this human disease.
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
     FGFR2* Fgfr2* View 6 models HomoloGene and HGNC
References Disease References using Mouse Models (10)

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
09/13/2016
MGI 6.05
The Jackson Laboratory