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The protein encoded by this gene upregulates trancriptional activation by the Wilms tumor protein and interacts witHuman, Mouseany other proteins, including CTNNB1, APC, AXIN1, and AXIN2. Defects in this gene are a cause of osteopathia striata with cranial sclerosis (OSCS). Protein function: Regulator of the canonical Wnt signaling pathway. Acts by specifically binding phosphatidylinositol 4,5-bisphosphate (PtdIns(4,5)P2), translocating to the cell membrane and interacting with key regulators of the canonical Wnt signaling pathway, such as components of the beta-catenin destruction complex. Acts both as a positive and negative regulator of the Wnt signaling pathway, depending on the context: acts as a positive regulator by promoting LRP6 phosphorylation. Also acts as a negative regulator by acting as a scaffold protein for the beta- catenin destruction complex and promoting stabilization of Axin at the cell membrane. Promotes CTNNB1 ubiquitination and degradation. Involved in kidney development. [The UniProt Consortium]
Keywords:
Anti-Amer1, Anti-AMER1, Anti-FAM123B, Anti-Protein FAM123B, Anti-APC membrane recruitment protein 1, Anti-Wilms tumor gene on the X chromosome protein, AMER1 Polyclonal Antibody
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