Bartter syndrome, infantile, with sensorineural deafness (Barttin), also known as BSND, is a human gene which is associated with Bartter syndrome. [5] This gene encodes an essential …

2024年12月24日 · BSND (Barttin CLCNK Type Accessory Subunit Beta) is a Protein Coding gene. Diseases associated with BSND include Bartter Syndrome, Type 4A, Neonatal, With …

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The BSND gene provides instructions for making a protein called barttin. This protein is found primarily in the kidneys, where it attaches (binds) to two specific chloride channels: ClC-Ka …

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2009年10月15日 · The human BSND cDNA consists of 1,596 basepairs and encodes a protein, designated barttin, that contains 2 putative transmembrane alpha helices. There is 70% amino …

BSND encodes a protein expressed in cells of the inner ear that maintain endocochlear potential. The function of DSPP is unknown, although its pattern of expression in teeth and the inner ear …

Regulatory subunit of anion-selective CLCNKA:BSND and CLCNKB:BSND heteromeric channels involved in basolateral chloride conductance along the nephron to achieve urine concentration …

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