CLCN5
id:
clcn5-170-11625143
title:
CLCN5
text:
The CLCN5 gene encodes the chloride channel Cl-/H+ exchanger ClC-5. ClC-5 is mainly expressed in the kidney, in particular in proximal tubules where it participates to the uptake of albumin and low-molecular-weight proteins, which is one of the principal physiological role of proximal tubular cells. Mutations in the CLCN5 gene cause an X-linked recessive nephropathy named Dent disease characterized by excessive urinary loss of low-molecular-weight proteins and of calcium (hypercalciuria), nephro
brand slug:
wiki
category slug:
encyclopedia
description:
Mammalian protein found in humans
original url:
https://en.wikipedia.org/wiki/CLCN5
date created:
2007-11-10T00:04:11Z
date modified:
2024-09-01T02:57:34Z
main entity:
{"identifier":"Q21100771","url":"https://www.wikidata.org/entity/Q21100771"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/8/81/Protein_CLCN5_PDB_2j9l.png","width":855,"height":944}
fields total:
13
integrity:
16