Table 6 Summary of the same com-abnormal genes discovered by eight methods
Gene ID | Gene ED | Related GO annotations | Related diseases | Relevance score |
|---|---|---|---|---|
3880 | KRT19 | Structural molecule activity and structural constituent of cytoskeleton | Lung cancer and thyroid cancer | 31.72, 24.50, 20.66 |
1508 | CTSB | Peptidase activity and cysteine-type peptidase activity | Keratolytic winter erythema and occlusion of gallbladder | 24.10, 10.61, 1.22 |
2778 | GNAS | GTP binding and signal transducer activity | McCune-Albright syndrome, somatic, mosaic, and pseudohypoparathyroidism Ia | 28.52, 9.69, 1.78 |
3852 | KRT5 | Structural molecule activity and scaffold protein binding | Epidermolysis bullosa simplex, Dowling-Meara type and epidermolysis bullosa simplex, Weber-Cockayne type | 24.03, 13.77, 0.17 |
6277 | S100A6 | Calcium ion binding and calcium-dependent protein binding | Endometrial cancer and pancreatic cancer | 19.09, 6.61, 1.44 |
1277 | COL1A1 | Identical protein binding and platelet-derived growth factor binding | Caffey disease and osteogenesis imperfecta, type I | 8.85, 19.64, 1.22 |
9168 | TMSB10 | Actin binding and actin monomer binding | Actin binding and actin monomer binding | 3.31, 1.29, 1.22 |