🧬 基因注释：NPAP1
📝 官方信息
官方名称：nuclear pore associated protein 1
功能摘要：This intronless retrogene is located in the Prader-Willi syndrome region on chromosome 15. This gene exhibits tissue-specific imprinting. Expression in adult testis and brain is biallelic, while expression in fetal brain is monoallelic and only from the paternal chromosome. The encoded protein is associated with the nuclear pore complex. [provided by RefSeq, Mar 2021].
🎯 作为靶基因的剪接因子
- RBM20 置信度: 2.0
🏥 关联疾病
该基因暂无关联疾病记录