About   Help   FAQ
Human Disease and Mouse Model Detail
Human Disease Opitz-Kaveggia Syndrome; OKS
OMIM ID: 305450
Human Phenotype Ontology associations
Synonyms FG Syndrome; Fg Syndrome 1; FGS1; Fg Syndrome; FGS; Keller Syndrome; Mental Retardation, Large Head, Imperforate Anus, Congenital Hypotonia, and Partial Agenesis of Corpus Callosum
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
     MED12* Med12   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
MGI 6.07
The Jackson Laboratory