BSND Products

Description

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. [provided by RefSeq]

Bioinformatics

Entrez	7809 Human
Uniprot	NP_476517.1 Human
Product By Gene ID	7809
Alternate Names	BARTMGC119284 Bartter syndrome, infantile, with sensorineural deafness (Barttin) barttin deafness, autosomal recessive 73 DFNB73 MGC119283 MGC119285