The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KCNE1-20-RE | 20 (40 μL) | 200 μL |  |
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| KCNE1-20-OR | 20 (40 μL) | 200 μL |  |
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| KCNE1-20-GO | 20 (40 μL) | 200 μL |  |
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| KCNE1-20-GR | 20 (40 μL) | 200 μL |  |
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| KCNE1-20-AQ | 20 (40 μL) | 200 μL |  |
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The product of this gene belongs to the potassium channel KCNE family. Potassium ion channels are essential to many cellular functions and show a high degree of diversity, varying in their electrophysiologic and pharmacologic properties. This gene encodes a transmembrane protein known to associate with the product of the KVLQT1 gene to form the delayed rectifier potassium channel. Mutation in this gene are associated with both Jervell and Lange-Nielsen and Romano-Ward forms of long-QT syndrome. Alternatively spliced transcript variants encoding the same protein have been identified. [provided by RefSeq, Jul 2008]
Gene Symbol : KCNE1
Gene Name : Potassium voltage-gated channel subfamily E regulatory subunit 1
Chromosome : CHR 21: 345,122,74-344,466,87
Locus : 21q22.12
Alt. Genes : DHRS9
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