Human Disease and Mouse Model Detail
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Human Disease
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Branchiooculofacial Syndrome; BOFS
OMIM ID: 113620
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Synonyms
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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
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Genes and
mouse models
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Mutations in human and/or mouse homologs are associated with this disease
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*Gene is associated with the disease in this species |
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Tfap2a
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TFAP2A*
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1:1 Homology
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Analysis Tools