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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).
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: autosomal dominant polycystic kidney disease type II; Autosomal dominant polycystic kidney disease type II protein; PC2; PKD2; polycystic kidney disease 2 (autosomal dominant); Polycystic kidney disease 2 protein; Polycystin-2; Polycystwin; R48321; Transient receptor potential cation channel subfamily P member 2; unnamed protein product
基因别名: APKD2; Pc-2; PC2; PKD2; PKD4; TRPP1; TRPP2
UniProt ID: (Human) Q13563
Entrez Gene ID: (Human) 5311