🧬 基因注释：KCTD17
📝 官方信息
官方名称：potassium channel tetramerization domain containing 17
功能摘要：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].
🎯 作为靶基因的剪接因子
- CPSF7 置信度: 2.0
- CSTF2T 置信度: 2.0
- GRSF1 置信度: 2.0
- HNRNPH1 置信度: 2.0
- HNRNPK 置信度: 2.0
- MBNL1 置信度: 2.0
- NOVA1 置信度: 2.0
- PTBP1 置信度: 2.0
- RBFOX2 置信度: 2.0
- RBM15 置信度: 2.0
- FUS 置信度: 1.0
- Mbnl2 置信度: 1.0
- NXF1 置信度: 1.0
- PCBP2 置信度: 1.0
- PRPF8 置信度: 1.0
- Rbmx 置信度: 1.0
- Srsf2 置信度: 1.0
- Srsf3 置信度: 1.0
- Tardbp 置信度: 1.0
- Tra2a 置信度: 1.0
🏥 关联疾病
该基因暂无关联疾病记录