🧬 基因注释：XK
📝 官方信息
官方名称：X-linked Kx blood group antigen, Kell and VPS13A binding protein
功能摘要：This locus controls the synthesis of the Kell blood group 'precursor substance' (Kx). Mutations in this gene have been associated with McLeod syndrome, an X-linked, recessive disorder characterized by abnormalities in the neuromuscular and hematopoietic systems. The encoded protein has structural characteristics of prokaryotic and eukaryotic membrane transport proteins. [provided by RefSeq, Jul 2008].
🎯 作为靶基因的剪接因子
- CPSF6 置信度: 2.0
- CSTF2 置信度: 2.0
- CSTF2T 置信度: 2.0
- EWSR1 置信度: 2.0
- HNRNPA2B1 置信度: 2.0
- HNRNPC 置信度: 2.0
- HNRNPL 置信度: 2.0
- HNRNPU 置信度: 2.0
- PTBP1 置信度: 2.0
- AQR 置信度: 1.0
- NXF1 置信度: 1.0
- Nova2 置信度: 1.0
- PRPF8 置信度: 1.0
- Ptbp2 置信度: 1.0
- Rbm7 置信度: 1.0
- Rbpms 置信度: 1.0
- Tardbp 置信度: 1.0
- U2af2 置信度: 1.0
- UPF1 置信度: 1.0
- YBX1 置信度: 1.0
🏥 关联疾病
该基因暂无关联疾病记录