🧬 基因注释：DCDC2
📝 官方信息
官方名称：doublecortin domain containing 2
功能摘要：This gene encodes a doublecortin domain-containing family member. The doublecortin domain has been demonstrated to bind tubulin and enhance microtubule polymerization. This family member is thought to function in neuronal migration where it may affect the signaling of primary cilia. Mutations in this gene have been associated with reading disability (RD) type 2, also referred to as developmental dyslexia. Alternatively spliced transcript variants encoding the same protein have been found for this gene. [provided by RefSeq, Jan 2013].
🎯 作为靶基因的剪接因子
- CPSF4 置信度: 2.0
- CPSF7 置信度: 2.0
- CSTF2T 置信度: 2.0
- HNRNPA1 置信度: 2.0
- HNRNPC 置信度: 2.0
- HNRNPK 置信度: 2.0
- HNRNPL 置信度: 2.0
- HNRNPM 置信度: 2.0
- HNRNPU 置信度: 2.0
- KHSRP 置信度: 2.0
- RBFOX2 置信度: 2.0
- RBM10 置信度: 2.0
- RBM20 置信度: 2.0
- AQR 置信度: 1.0
- CPSF1 置信度: 1.0
- CPSF2 置信度: 1.0
- CPSF3 置信度: 1.0
- FUS 置信度: 1.0
- MATR3 置信度: 1.0
- NXF1 置信度: 1.0
🏥 关联疾病
该基因暂无关联疾病记录