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CLCN5

2J9L, 2JA3118412728ENSG00000171365ENSMUSG00000004317P51795Q9WVD4NM_000084NM_001127898NM_001127899NM_001272102NM_001282163NM_001243762NM_016691NP_000075NP_001121370NP_001121371NP_001259031NP_001269092NP_001230691NP_057900H(+)/Cl(-) exchange transporter 5 is a protein that in humans is encoded by the CLCN5 gene.2j9l: CYTOPLASMIC DOMAIN OF THE HUMAN CHLORIDE TRANSPORTER CLC-5 IN COMPLEX WITH ATP2ja3: CYTOPLASMIC DOMAIN OF THE HUMAN CHLORIDE TRANSPORTER CLC-5 IN COMPLEX WITH ADP H(+)/Cl(-) exchange transporter 5 is a protein that in humans is encoded by the CLCN5 gene. This gene encodes a member of the ClC family of chloride ion channels and ion transporters. Mutations in this gene have been found in Dent's Disease and renal tubular disorders complicated by nephrolithiasis. Although a member of a family of chloride channels, the CLCN5 protein allows movement of protons in the opposite direction of Cl(-), thus functioning as an antiporter.}} This article incorporates text from the United States National Library of Medicine, which is in the public domain.

[ "Hypercalciuria", "Kidney disease", "Proteinuria", "Nephrocalcinosis", "Phenotype", "CLCN5 gene" ]
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