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Human Disease and Mouse Model Detail
Human Disease Clubfoot, Congenital, with or without Deficiency of Long Bones and/or Mirror-Image Polydactyly; CCF
OMIM ID: 119800
Human Phenotype Ontology associations
View all models View ALL (11) 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
     PITX1* Pitx1* View 1 model HomoloGene
     cl* View 1 model
Dbf* View 1 model
FKBP8 Fkbp8* View 1 model HomoloGene and HGNC
FRAS1 Fras1* View 1 model HomoloGene and HGNC
GRIP1 Grip1* View 1 model HomoloGene
pma* View 1 model
RET Ret* View 1 model HomoloGene and HGNC
skc3* View 1 model
TCIRG1 Tcirg1* View 1 model HomoloGene and HGNC
vsd* View 1 model
References Disease References using Mouse Models (11)

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 6.05
The Jackson Laboratory