🧬 基因注释：SIX1
📝 官方信息
官方名称：SIX homeobox 1
功能摘要：The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3). [provided by RefSeq, Jul 2008].
🎯 作为靶基因的剪接因子
- CPSF6 置信度: 2.0
- CPSF7 置信度: 2.0
- CSTF2 置信度: 2.0
- CSTF2T 置信度: 2.0
- GRSF1 置信度: 2.0
- HNRNPA2B1 置信度: 2.0
- HNRNPC 置信度: 2.0
- HNRNPH1 置信度: 2.0
- MBNL1 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
- PRPF8 置信度: 1.0
- Rbmx 置信度: 1.0
- Tardbp 置信度: 1.0
- U2af1 置信度: 1.0
- UPF1 置信度: 1.0
- YBX1 置信度: 1.0
- fus 置信度: 1.0
🏥 关联疾病
该基因暂无关联疾病记录