KvLQT2

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potassium voltage-gated channel, KQT-like subfamily, member 2
Identifiers
Symbol KCNQ2
Alt. Symbols EBN, EBN1
Entrez 3785
HUGO 6296
OMIM 602235
RefSeq NM_172109
UniProt O43526
Other data
Locus Chr. 20 q13.33

KvLQT2 (Kv7.2) is a potassium channel protein coded for by the gene KCNQ2.

It is associated with benign familial neonatal convulsions.

External links

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Membrane transport protein: ion channels
Ca2+: Calcium channelVoltage-dependent calcium channel (L-type/Cav1.2, Cav2.1, N-type, P-type, Q-type, R-type, T-type) - Inositol triphosphate receptor - Ryanodine receptor - Cation channels of sperm - Two-pore channel
Na+: Sodium channelNav1.4 - Nav1.5 - Nav1.7- Nav1.9 - Epithelial sodium channel
K+: Potassium channelVoltage-gated (Kv1.1, KvLQT1, KvLQT2, KvLQT3, HERG, Shaker gene, KCNE1) - Calcium-activated (BK channel, SK channel, SK3) - Inward-rectifier (ROMK, Kir2.1, KCNJ11) - Tandem pore domain
Cl-: Chloride channelCystic fibrosis transmembrane conductance regulator
PorinAquaporin (1, 2, 3, 4) - Voltage-dependent anion channel
Cations: TRPTRPA - TRPC (TRPC6) - TRPM (TRPM6) - TRPML (Mucolipin-1) - TRPP - TRPV (TRPV1, TRPV6)
Other/generalVoltage-gated ion channel - Ligand-gated ion channel - Cyclic nucleotide-gated ion channel - Stretch-activated ion channel
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