BSND, barttin CLCNK type accessory subunit beta

BSND, barttin CLCNK type accessory subunit beta

• 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, Jul 2008]

• Gene Synonyms (barttin, Bartter syndrome, infantile, with sensorineural deafness (Barttin), barttin CLCNK type accessory beta subunit, barttin CLCNK-type chloride channel accessory beta subunit, deafness, autosomal recessive 73, BART, DFNB73,)
• NCBI Gene ID: 7809
• Species: Homo sapiens (Human)
• UNIPROT ID#>>Q5VU50
  UNIPROT ID#>>Q8WZ55
• View the NCBI Database for this Gene »

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

barttin CLCNK type accessory subunit beta interacts with:

• adiponectin, C1Q and collagen domain containing
  ADP ribosylation factor interacting protein 1
  apolipoprotein L2
  bone morphogenetic protein 10
  CDP-diacylglycerol--inositol 3-phosphatidyltransferase
  ceramide transporter 1
  chondroitin sulfate N-acetylgalactosaminyltransferase 2
  Ecm29 proteasome adaptor and scaffold
  fetal and adult testis expressed 1
  jagunal homolog 1
  MYG1 exonuclease
  phospholipid scramblase 2
  solute carrier family 30 member 8
  SPG21 abhydrolase domain containing, maspardin
  syntaxin 8
  THAP domain containing 4
  transforming growth factor beta regulator 4
  transmembrane protein 60
  vesicle associated membrane protein 3

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.