Disease:Defects in LRP6 are the cause of autosomal dominant coronary artery disease type 2 (ADCAD2) [MIM:610947]. ,Domain:The YWTD-EGF-like domains 1 and 2 are required for the interaction with Wnt-frizzled complex. The YWTD-EGF-like domains 3 and 4 are required for the interaction with DKK1. ,Function:Essential for the Wnt/beta catenin signaling pathway , probably by acting as a coreceptor together with Frizzled for Wnt. Specific high-affinity receptor for DKK1 and DKK2 , but not DKK3. The interaction with DKK1 blocks LRP6-mediated Wnt/beta catenin signaling via LRP6 removal via Kremen proteins-mediated endocytosis. ,similarity:Belongs to the LDLR family. ,similarity:Contains 20 LDL-receptor class B repeats. ,similarity:Contains 3 LDL-receptor class A domains. ,similarity:Contains 4 EGF-like domains. ,subunit:Interacts with RSPO1 and RSPO3 (By similarity) . Interacts with FZD5. Essential component of the Wnt7 receptor complex. Wnt7A interacts with the LRP6/FZD5 complex. This interaction is antagonized by DKK1 and DKK3. ,tissue specificity:Widely co-expressed with LRP5 during embryogenesis and in adult tissues. ,
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