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Human Disease and Mouse Model Detail
Human Disease Klippel-Feil Syndrome 1, Autosomal Dominant; KFS1
OMIM ID: 118100
Synonyms Cervical Vertebral Fusion, Autosomal Dominant; Kfs; Klippel-Feil Syndrome
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
     Gdf6 GDF6*   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
12/16/2014
MGI 5.20
The Jackson Laboratory