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BSND

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BSND
Identifiers
AliasesBSND, BART, DFNB73, barttin CLCNK type accessory beta subunit, barttin CLCNK type accessory subunit beta
External IDsOMIM: 606412; MGI: 2153465; HomoloGene: 14291; GeneCards: BSND; OMA:BSND - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_057176

NM_080458

RefSeq (protein)

NP_476517

NP_536706

Location (UCSC)Chr 1: 55 – 55.02 MbChr 4: 106.34 – 106.35 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

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 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.[5]

References

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  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000162399Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000025418Ensembl, May 2017
  3. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ^ a b "BSND barttin CLCNK type accessory subunit beta [ Homo sapiens (human) ]".
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Further reading

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