🧬 基因注释：PJVK
📝 官方信息
官方名称：pejvakin
功能摘要：The protein encoded by this gene is a member of the gasdermin family, a family which is found only in vertebrates. The encoded protein is required for the proper function of auditory pathway neurons. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal recessive type 59 (DFNB59). [provided by RefSeq, Dec 2008].
🎯 作为靶基因的剪接因子
- CPSF7 置信度: 2.0
- EIF4A3 置信度: 2.0
- GRSF1 置信度: 2.0
- HNRNPA2B1 置信度: 2.0
- PABPC4 置信度: 2.0
- PTBP1 置信度: 2.0
- RBFOX2 置信度: 2.0
- RBM10 置信度: 2.0
- RBM15 置信度: 2.0
- Rbm7 置信度: 1.0
- Rbmx 置信度: 1.0
- Rnps1 置信度: 1.0
- SRSF2 置信度: 1.0
- SRSF3 置信度: 1.0
- Srsf1 置信度: 1.0
- Srsf7 置信度: 1.0
- TIA1 置信度: 1.0
- Tardbp 置信度: 1.0
- Tra2a 置信度: 1.0
- U2af1 置信度: 1.0
🏥 关联疾病
该基因暂无关联疾病记录