This gene encodes a protein that belongs to a conserved family of potassium channel tetramerization domain (KCTD)-containing proteins. The encoded protein functions in ciliogenesis by acting as a substrate adaptor for the cullin3-based ubiquitin-conjugating enzyme E3 ligase, and targets trichoplein, a keratin-binding protein, for degradation via polyubiquitinylation. A mutation in this gene is associated with autosomal dominant myoclonic dystonia 26. [provided by RefSeq, Nov 2016]
| SKU | Test Kits | Buffer | Dye Color | Order Now |
|---|---|---|---|---|
| KCTD17-20-RE | 20 (40 μL) | 200 μL |  |
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| KCTD17-20-OR | 20 (40 μL) | 200 μL |  |
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| KCTD17-20-GO | 20 (40 μL) | 200 μL |  |
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| KCTD17-20-GR | 20 (40 μL) | 200 μL |  |
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| KCTD17-20-AQ | 20 (40 μL) | 200 μL |  |
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This gene encodes a protein that belongs to a conserved family of potassium channel tetramerization domain (KCTD)-containing proteins. The encoded protein functions in ciliogenesis by acting as a substrate adaptor for the cullin3-based ubiquitin-conjugating enzyme E3 ligase, and targets trichoplein, a keratin-binding protein, for degradation via polyubiquitinylation. A mutation in this gene is associated with autosomal dominant myoclonic dystonia 26. [provided by RefSeq, Nov 2016]
Gene Symbol : KCTD17
Gene Name : Potassium channel tetramerization domain containing 17
Chromosome : CHR 22: 370,517,24-370,633,89
Locus : 22q12.3
Alt. Genes : ABI2
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