NCBI Description of FAM123B
|The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts with many other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS).|
Community Annotation of FAM123B Add / Edit FAM123B: Annotations
No community annotations yet for FAM123B.
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