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🔬 剪接因子 HNRNPK 靶基因疾病富集分析
| 疾病名称 | Overlap | P-value | 富集倍数 | 相关靶基因 |
|---|---|---|---|---|
| Intellectual disability | 29/57 | 0.012539 | 1.41x | SNRPB, SRSF1, HNRNPK, U2AF2, SF3B4, FMR1, DDX17, PABPC1, PQBP1, DHX30, HNRNPUL2, ZFR, UPF1, THOC2, FAM50A, HNRNPU, PUF60, CDK10, LSM1, ZMYM3 |
| autism | 7/9 | 0.013167 | 2.15x | DHX30, PPIL2, SNRPN, THOC2, NONO, FMR1, XRN2 |
| Global developmental delay | 12/20 | 0.023942 | 1.66x | CDK10, AAR2, PABPC1, DHX30, DDX5, LSM1, SNRNP70, UPF1, ZMYM3, DDX6, DDX3X, EFTUD2 |
| microcephaly | 8/12 | 0.030144 | 1.84x | PQBP1, AAR2, DHX30, ADAR, DHX34, RBM28, DDX3X, TRA2B |
| gastric intestinal type adenocarcinoma | 21/41 | 0.030295 | 1.42x | FUS, THRAP3, RNF213, A1CF, PABPC1, EWSR1, HNRNPA2B1, QKI, NUMA1, U2AF1, ZMYM3, FUBP1, NONO, SRSF2, DDX5, SPEN, RBM10, DDX6, DDX3X, SND1 |
| skin angiosarcoma | 3/3 | 0.047021 | 2.76x | SND1, DDX3X, RNF213 |
| acrocephalosyndactyly | 3/3 | 0.047021 | 2.76x | NCBP2, POLR2G, NCBP1 |
💡 说明:
• Overlap: 靶基因中与该疾病相关的基因数 / 数据库中该疾病总关联基因数
• P-value: 超几何检验显著性,越小代表富集越显著
• 富集倍数: 实际关联数 / 期望关联数,>1 表示富集
• Overlap: 靶基因中与该疾病相关的基因数 / 数据库中该疾病总关联基因数
• P-value: 超几何检验显著性,越小代表富集越显著
• 富集倍数: 实际关联数 / 期望关联数,>1 表示富集