KCNE1
From Wikipedia, the free encyclopedia
potassium voltage-gated channel, Isk-related family, member 1
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Identifiers | |
Symbol | KCNE1 |
HUGO | 6240 |
Entrez | 3753 |
OMIM | 176261 |
RefSeq | NM_000219 |
UniProt | P15382 |
Other data | |
Locus | Chr. 21 q22.1-22.2 |
KCNE1 is a gene associated with Long QT syndrome type 5. It can both cause Romano-Wards syndrome (heterozygotes) and Jervell Lange-Nielsens syndrome (homozygotes)
[edit] See also
[edit] External links
Stretch-activated ion channel - Ligand-gated ion channel - Voltage-gated ion channel
Ca: Voltage-dependent calcium channel (L-type/CACNA1C, N-type, P-type, Q-type, R-type, T-type) - Inositol triphosphate receptor - Ryanodine receptor - Cation channels of sperm
Na: Sodium channel: SCN4A - SCN5A - SCN9A - Epithelial sodium channel
K: Potassium channel: Voltage-gated (KvLQT1, HERG, Shaker gene, KCNE1) - Calcium-activated (BK channel, SK channel) - Inward-rectifier (ROMK, KCNJ2) - Tandem pore domain/Resting ion channel
Cl: Chloride channel: Cystic fibrosis transmembrane conductance regulator
Transient receptor potential (TRPV6) - Cyclic nucleotide-gated ion channel - Two-pore channel