🧬 基因注释：SRSF1
📝 官方信息
官方名称：serine and arginine rich splicing factor 1
功能摘要：This gene encodes a member of the arginine/serine-rich splicing factor protein family. The encoded protein can either activate or repress splicing, depending on its phosphorylation state and its interaction partners. Multiple transcript variants have been found for this gene. There is a pseudogene of this gene on chromosome 13. [provided by RefSeq, Jun 2014].
🎯 作为靶基因的剪接因子
- HNRNPC 综合评分: 0.546 · 证据 2 条
- FUS 综合评分: 0.474 · 证据 1 条
- fus 综合评分: 0.474 · 证据 1 条
- HNRNPA1 综合评分: 0.448 · 证据 2 条
- Srsf3 综合评分: 0.444 · 证据 1 条
- Tardbp 综合评分: 0.441 · 证据 1 条
- SRSF9 综合评分: 0.424 · 证据 1 条
- Srsf2 综合评分: 0.424 · 证据 1 条
- FUBP1 综合评分: 0.410 · 证据 2 条
- TIA1 综合评分: 0.374 · 证据 1 条
- HNRNPU 综合评分: 0.362 · 证据 2 条
- PTBP1 综合评分: 0.362 · 证据 2 条
- HNRNPA2B1 综合评分: 0.350 · 证据 2 条
- HNRNPF 综合评分: 0.350 · 证据 2 条
- HNRNPH1 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
- QKI 综合评分: 0.350 · 证据 1 条
- CELF2 综合评分: 0.336 · 证据 2 条
- Ptbp2 综合评分: 0.324 · 证据 1 条
🏥 关联疾病
neurodevelopmental disorder with dysmorphic facies and behavioral abnormalities
中关联 (0.615)
Neurodevelopmental delay
中关联 (0.538)
Intellectual disability
中关联 (0.534)
neurodegenerative disease
中关联 (0.501)
dengue disease
低关联 (0.370)
genetic disorder
低关联 (0.333)
hypothyroidism
低关联 (0.122)
autism spectrum disorder
低关联 (0.118)
frozen shoulder
低关联 (0.116)
cancer
低关联 (0.105)