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Human Disease and Mouse Model Detail
Human Disease Branchiooculofacial Syndrome; BOFS
OMIM ID: 113620
Synonyms Bof Syndrome; Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging; Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome; Lip Pseudocleft-Hemangiomatous Branchial Cyst 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
     Tfap2a TFAP2A*   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
07/15/2014
MGI 5.18
The Jackson Laboratory