KvLQT1

KCNQ1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesKCNQ1, ATFB1, ATFB3, JLNS1, KCNA8, KCNA9, KVLQT1, Kv1.9, Kv7.1, LQT, LQT1, RWS, SQT2, WRS, potassium voltage-gated channel subfamily Q member 1
External IDsOMIM: 607542; MGI: 108083; HomoloGene: 85014; GeneCards: KCNQ1; OMA:KCNQ1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

3784

16535

Ensembl

ENSG00000282076
ENSG00000053918

ENSMUSG00000009545

UniProt

P51787

P97414

RefSeq (mRNA)

NM_181798
NM_000218
NM_181797

NM_008434

RefSeq (protein)

NP_000209
NP_861463

NP_032460

Location (UCSC)Chr 11: 2.44 – 2.85 MbChr 7: 142.66 – 142.98 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Kv7.1 (KvLQT1) is a potassium channel protein whose primary subunit in humans is encoded by the KCNQ1 gene. Its mutation causes Long QT syndrome, Kv7.1 is a voltage and lipid-gated potassium channel present in the cell membranes of cardiac tissue and in inner ear neurons among other tissues. In the cardiac cells, Kv7.1 mediates the IKs (or slow delayed rectifying K+) current that contributes to the repolarization of the cell, terminating the cardiac action potential and thereby the heart's contraction. It is a member of the KCNQ family of potassium channels.