BSND
id:
bsnd-240-10868509
title:
BSND
text:
Bartter syndrome, infantile, with sensorineural deafness (Barttin), also known as BSND, is a human gene which is associated with Bartter syndrome. This gene encodes an essential beta subunit for CLC chloride channels. These heteromeric channels localize to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. Mutations in this gene have been associated with Bartter syndrome with sensorineural deafness.
brand slug:
wiki
category slug:
encyclopedia
description:
Protein-coding gene in the species Homo sapiens
original url:
https://en.wikipedia.org/wiki/BSND
date created:
date modified:
2024-01-09T04:38:08Z
main entity:
{"identifier":"Q18032616","url":"https://www.wikidata.org/entity/Q18032616"}
image:
{"content_url":"https://upload.wikimedia.org/wikipedia/commons/d/d6/Ideogram_human_chromosome_1.svg","width":474,"height":189}
fields total:
13
integrity:
15