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KCNQ1

This gene encodes a voltage-gated potassium channel necessary for the cardiac action potential's repolarization phase. Together with KCNE1 and KCNE3, two additional potassium channel proteins, this protein can form heteromultimers. Hereditary long QT syndrome 1, also known as Romano-Ward syndrome, Jervell and Lange-Nielsen syndrome, and familial atrial fibrillation are all linked to mutations in this gene. The expression of this gene is tissue-specific, preferentially coming from the maternal allele in some tissues while being biallelic in others.

Full Name Potassium voltage-gated channel subfamily Q member 1
Gene ID Human: 3784
Mouse: 16535
Rat: 84020
Monkey: 721211
UniProt ID Human: P51787
Mouse: P97414
Rat: Q9Z0N7
Monkey: F7C2U7
Alternative Names LQT; RWS; WRS; LQT1; SQT2; ATFB1; ATFB3; JLNS1; KCNA8; KCNA9; Kv1.9; Kv7.1; KVLQT1; potassium voltage-gated channel subfamily KQT member 1; IKs producing slow voltage-gated; potassium channel subunit alpha KvLQT1; kidney and cardiac voltage dependend K+ channel; potassium channel, voltage gated KQT-like subfamily Q, member 1; potassium voltage-gated channel, KQT-like subfamily, member 1; slow delayed rectifier channel subunit; voltage-gated potassium channel subunit Kv7.1; KCNQ1; Potassium voltage-gated channel subfamily Q member 1

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Product Category:
Membrane Protein Stable Cell Lines
Target Protein: KCNQ1/KCNE1 Target Family: Voltage Gated Potassium Channel Target Protein Species: Human
Product Category:
Membrane Protein Stable Cell Lines
Target Protein: KCNQ1 Target Family: Kv7 Target Protein Species: Human Host Cell Type: CHO-K1; HEK293
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