This gene encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KCTD7-20-RE | 20 (40 μL) | 200 μL |  |
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| KCTD7-20-OR | 20 (40 μL) | 200 μL |  |
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| KCTD7-20-GO | 20 (40 μL) | 200 μL |  |
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| KCTD7-20-GR | 20 (40 μL) | 200 μL |  |
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| KCTD7-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a member of the potassium channel tetramerization domain-containing protein family. Family members are identified on a structural basis and contain an amino-terminal domain similar to the T1 domain present in the voltage-gated potassium channel. Mutations in this gene have been associated with progressive myoclonic epilepsy-3. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Jan 2011]
Gene Symbol : KCTD7
Gene Name : Potassium channel tetramerization domain containing 7
Chromosome : CHR 7: 666,288,80-666,432,28
Locus : 7q11.21
Alt. Genes : LINC01587
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