CLCNKB

Protein-coding gene in humans From Wikipedia, the free encyclopedia

Chloride channel Kb, also known as CLCNKB, is a protein which in humans is encoded by the CLCNKB gene.[5][6]

AliasesCLCNKB, CLCKB, ClC-K2, ClC-Kb, chloride voltage-gated channel Kb
End16,057,311 bp[1]
Quick facts Identifiers, Aliases ...
CLCNKB
Identifiers
AliasesCLCNKB, CLCKB, ClC-K2, ClC-Kb, chloride voltage-gated channel Kb
External IDsOMIM: 602023; MGI: 1329026; HomoloGene: 65; GeneCards: CLCNKB; OMA:CLCNKB - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000085
NM_001165945

NM_001146307
NM_024412

RefSeq (protein)

NP_000076
NP_001159417

NP_001139779
NP_077723

Location (UCSC)Chr 1: 16.04 – 16.06 MbChr 4: 141.11 – 141.13 Mb
PubMed search[3][4]
Wikidata
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Chloride channel Kb (CLCNKB) is a member of the CLC family of voltage-gated chloride channels, which comprises at least 9 mammalian chloride channels.[7] Each is believed to have 12 transmembrane domains and intracellular N and C termini. Mutations in CLCNKB result in the autosomal recessive Type III Bartter syndrome.[8] CLCNKA and CLCNKB are closely related (94% sequence identity), tightly linked (separated by 11 kb of genomic sequence) and are both expressed in mammalian kidney.[5]

See also

References

Further reading

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