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 |
Product List
- 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