🧬 基因注释：NXNL1
📝 官方信息
官方名称：nucleoredoxin like 1
功能摘要：Retinitis pigmentosa (RP) is a disease that leads to blindness by degeneration of cone photoreceptors. Rods produce factors required for cone viability. The protein encoded by this gene is one of those factors and is similar to a truncated form of thioredoxin. This gene has been proposed to have therapeutic value against RP. [provided by RefSeq, Dec 2015].
🎯 作为靶基因的剪接因子
- HNRNPC 置信度: 2.0
🏥 关联疾病
该基因暂无关联疾病记录