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Tyrosine-protein kinase transmembrane receptor ROR2 is a type I transmembrane protein and a member of the receptor tyrosine kinases (RTKs). It acts as a cell surface receptor involved in noncanonical WNT signaling, particularly mediating WNT5A signaling to regulate tissue morphogenesis. ROR2 plays essential roles in early chondrocyte formation, cartilage and growth plate development, bone and cartilage growth during embryonic development, and modulation of neurite outgrowth and branching in hippocampal neurons. Mutations or dysfunctions in the ROR2 gene/protein are associated with several developmental disorders including Robinow syndrome and Brachydactyly type B, and have been implicated in metastatic diseases. It contains a cysteine-rich domain (CRD) and a Kringle domain that are critical for ligand binding and function.
WNT5A-dependent signal transduction, modulation of DVL phosphorylation, gene expression changes
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