| Entrez gene ID | | 7809 |
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| Official gene symbol | | BSND |
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| Full name | | Bartter syndrome, infantile, with sensorineural deafness (Barttin) |
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| Aliases | | ,BART,DFNB73,MGC119283,MGC119284,MGC119285, |
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| Gene summary | | 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] |
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| Location | | Chromosome: 1 Locus: 1p32.1 |
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| Gene position | | 55464617 - 55474465 Map Viewer |
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| Gene orientation | | plus |
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| Gene size | | 9849 bp |
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| Gene sequence |
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| OMIM ID | | 606412 |
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