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🔬 剪接因子 YBX1 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 |
|---|---|---|---|---|
| neurodegenerative disease | 177/422 | 0.002141 | 1.11x | RBM15B, SF3B1, SRSF1, RBM38, DHX38, SAMD4B, RBM22, HNRNPK, RBM17, PRPF19, DDX17, PABPC1, MBNL1, BUD13, DHX30, LUC7L3, SART3, CTNNBL1, EIF4B, LSM4 |
| Intellectual disability | 30/57 | 0.012850 | 1.39x | SNRPB, SRSF1, HNRNPK, U2AF2, SF3B4, FMR1, DDX17, PABPC1, EIF4A3, PQBP1, DHX30, HNRNPUL2, THOC6, ZFR, UPF1, THOC2, FAM50A, HNRNPU, PUF60, ZMYM3 |
| angina pectoris | 4/4 | 0.020337 | 2.64x | SF3A3, RNF213, DHX38, BUD13 |
| Gastric Adenoma | 14/24 | 0.031206 | 1.54x | ZCCHC8, FUS, NUMA1, CRNKL1, SPEN, THRAP3, SFPQ, ZMYM3, RNF213, QKI, DDX6, DDX3X, SND1, PRCC |
| genetic disorder | 52/113 | 0.032902 | 1.21x | FUS, SNRPB, SRSF1, HNRNPK, IK, U2AF2, RNF213, PCBP1, SF3B4, PRPF19, FMR1, RNF34, EIF4A3, PQBP1, DHX30, HNRNPUL2, THOC6, ADAR, HNRNPA2B1, THOC2 |
| coronary atherosclerosis | 6/8 | 0.037128 | 1.98x | SF3A3, GPATCH3, ADAR, CPEB4, AGO2, BUD13 |
| medulloblastoma | 7/10 | 0.039582 | 1.85x | SF3B1, ZMYM3, RNF213, NONO, DDX6, CCAR1, DDX3X |
| microcephaly | 8/12 | 0.040177 | 1.76x | PQBP1, AAR2, DHX30, ADAR, DHX34, RBM28, DDX3X, TRA2B |
💡 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