🧬 基因注释：NONO
📝 官方信息
官方名称：non-POU domain containing octamer binding
功能摘要：This gene encodes an RNA-binding protein which plays various roles in the nucleus, including transcriptional regulation and RNA splicing. A rearrangement between this gene and the transcription factor E3 gene has been observed in papillary renal cell carcinoma. Alternatively spliced transcript variants have been described. Pseudogenes exist on Chromosomes 2 and 16. [provided by RefSeq, Feb 2009].
🎯 作为靶基因的剪接因子
- HNRNPL 综合评分: 0.444 · 证据 2 条
- Srsf3 综合评分: 0.444 · 证据 1 条
- HNRNPA2B1 综合评分: 0.412 · 证据 2 条
- Nova2 综合评分: 0.386 · 证据 1 条
- HNRNPK 综合评分: 0.362 · 证据 2 条
- PTBP1 综合评分: 0.362 · 证据 2 条
- SRSF9 综合评分: 0.362 · 证据 1 条
- Srsf2 综合评分: 0.362 · 证据 1 条
- HNRNPC 综合评分: 0.350 · 证据 2 条
- HNRNPF 综合评分: 0.350 · 证据 2 条
- HNRNPM 综合评分: 0.350 · 证据 2 条
- MBNL1 综合评分: 0.350 · 证据 2 条
- RBM10 综合评分: 0.312 · 证据 2 条
- TIA1 综合评分: 0.312 · 证据 1 条
- FUS 综合评分: 0.300 · 证据 1 条
- HNRNPD 综合评分: 0.300 · 证据 2 条
- HNRNPU 综合评分: 0.300 · 证据 2 条
- KHSRP 综合评分: 0.300 · 证据 2 条
- RBFOX2 综合评分: 0.300 · 证据 2 条
- SRSF2 综合评分: 0.300 · 证据 1 条
🏥 关联疾病
syndromic X-linked intellectual disability 34
高关联 (0.766)
syndromic intellectual disability
中关联 (0.555)
genetic disorder
中关联 (0.465)
X-linked intellectual disability - psychosis - macroorchidism
中关联 (0.462)
autism
低关联 (0.371)
X-linked syndromic intellectual disability
低关联 (0.370)
X-linked non-syndromic intellectual disability
低关联 (0.370)
Neurodevelopmental delay
低关联 (0.340)
renal carcinoma
低关联 (0.277)
congenital heart disease
低关联 (0.266)