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🔬 剪接因子 HNRNPU 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 |
|---|---|---|---|---|
| autism | 7/9 | 0.013521 | 2.14x | THOC2, NONO, FMR1, SNRPN, PPIL2, DHX30, XRN2 |
| breast carcinoma | 31/63 | 0.019180 | 1.35x | PSIP1, CPEB3, NONO, HNRNPA2B1, PRCC, SRSF3, CRNKL1, RBM15, FAM50A, DDX5, PABPC1, FUBP1, SF3B1, ZCCHC8, QKI, SPEN, DDX6, NUMA1, EWSR1, THRAP3 |
| HIV infection | 5/6 | 0.025975 | 2.29x | PSIP1, NCBP1, POLR2G, NCBP2, TAF15 |
| neurodegenerative disease | 165/422 | 0.026750 | 1.08x | PSIP1, CHERP, CDC5L, SRSF3, MATR3, HNRNPF, SART3, SAFB2, DBR1, RBM39, SRRM1, THOC5, RBM4, RBM27, RBMX, DDX6, PRPF19, ZRANB2, SNRPE, TRA2A |
| coronary atherosclerosis | 6/8 | 0.029914 | 2.06x | AGO2, SF3A3, CCNL1, BUD13, ADAR, CPEB4 |
| gastric ulcer | 3/3 | 0.047634 | 2.75x | SND1, RBM33, HNRNPLL |
| acrocephalosyndactyly | 3/3 | 0.047634 | 2.75x | NCBP1, POLR2G, NCBP2 |
💡 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