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Polycystin-2 (PC2), encoded by the PKD2 gene, is a multi-pass membrane protein that functions as a nonselective calcium-permeable cation channel, primarily localized to the primary cilium and endoplasmic reticulum. It plays a key role in calcium signaling and mechanosensation, often forming a complex with polycystin-1 to regulate cellular responses to fluid flow. Mutations in PKD2 disrupt these processes and lead to autosomal dominant polycystic kidney disease (ADPKD).
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Protein Aliases: autosomal dominant polycystic kidney disease type II; autosomal dominant polycystic kidney disease type II protein; PKD2; polycystic kidney disease 2 (autosomal dominant); transient receptor potential cation channel subfamily P member 2; unnamed protein product
Gene Aliases: APKD2; Pc-2; PC2; PKD4; TRPP2
UniProt ID: (Human) Q13563
Entrez Gene ID: (Human) 5311
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