KCNQ5

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

Potassium voltage-gated channel subfamily KQT member 5 is a protein that in humans is encoded by the KCNQ5 gene.[5][6][7][8]

AliasesKCNQ5, Kv7.5, potassium voltage-gated channel subfamily Q member 5, MRD46
End73,198,853 bp[1]
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KCNQ5
Identifiers
AliasesKCNQ5, Kv7.5, potassium voltage-gated channel subfamily Q member 5, MRD46
External IDsOMIM: 607357; MGI: 1924937; HomoloGene: 28270; GeneCards: KCNQ5; OMA:KCNQ5 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001160130
NM_001160132
NM_001160133
NM_001160134
NM_019842

NM_001160139
NM_023872
NM_001310477

RefSeq (protein)

NP_001153602
NP_001153604
NP_001153605
NP_001153606
NP_062816

NP_001153611
NP_001297406
NP_076361

Location (UCSC)Chr 6: 72.62 – 73.2 MbChr 1: 21.47 – 22.03 Mb
PubMed search[3][4]
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This gene is a member of the KCNQ potassium channel gene family that is differentially expressed in subregions of the brain and in skeletal muscle. The protein encoded by this gene yields currents that activate slowly with depolarization and can form heteromeric channels with the protein encoded by the KCNQ3 gene. Currents expressed from this protein have voltage dependences and inhibitor sensitivities in common with M-currents. They are also inhibited by M1 muscarinic receptor activation. Three alternatively spliced transcript variants encoding distinct isoforms have been found for this gene, but the full-length nature of only one has been determined.[8]

Interactions

KCNQ5 has been shown to interact with KvLQT3.[9]

See also

References

Further reading

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