This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KCNJ6BA-20-REGO | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-REGR | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-ORGR | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GOGR | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GRRE | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GROR | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-GRGO | 20 (40 μL) | 200 μL |
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| KCNJ6BA-20-AQOR | 20 (40 μL) | 200 μL |
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This gene encodes a member of the G protein-coupled inwardly-rectifying potassium channel family of inward rectifier potassium channels. This type of potassium channel allows a greater flow of potassium into the cell than out of it. These proteins modulate many physiological processes, including heart rate in cardiac cells and circuit activity in neuronal cells, through G-protein coupled receptor stimulation. Mutations in this gene are associated with Keppen-Lubinsky Syndrome, a rare condition characterized by severe developmental delay, facial dysmorphism, and intellectual disability. [provided by RefSeq, Apr 2015]
Gene Symbol : KCNJ6
Gene Name : Potassium voltage-gated channel subfamily J member 6
Chromosome : CHR 21: 379,164,37-376,242,22
Locus : 21q22.13
Alt. Genes : ZNF263
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