Description
Product Characteristics:
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).
Subcellular location: Cytoplasm, Nucleus, Cell membrane
Synonyms: AMER1, FAM 123B, Family with sequence similarity 123B, FLJ39827, OSCS, Protein FAM123B, RP11 403E24.2, Wilms tumor gene on the X chromosome protein, Wilms tumor on the X, WTX, AMER1_HUMAN.
Target Information: 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). [provided by RefSeq, May 2010]