Table 2.
Moleculesa | Total no of molecules | Score | Top diseases and functions |
---|---|---|---|
AGAP3, APOLD1, CALCR, CDKL1, EDIL3, FHL5, LEPR, LEPROT, NCOR2, TGFBR1 | 33 | 38 | connective tissue disorders, metabolic disease, cellular assembly and organization |
AMOTL2, API5, BICD1, DZIP1, ERK, FBF1, HEATR1, IFT122, NIN, TEX11 | 34 | 35 | cellular assembly, organization, morphology and maintenance |
GALR3, GPR6, GPR20, GPR26, GPR97, GPR98, LPHN3, LYST, MC2R, MC3R | 34 | 35 | cell signalling and interaction, cellular function and maintenance |
ABTB1, BRI3BP, CHD9, DDX18, DDX31, ESR1, FKBP7, GREB1, PPIL4, WHSC1 | 32 | 33 | organismal, embryonic and tissue development |
ACTR10, ANK2, APC2, DCTN4, DISC1, DNAH1, DNAH3, DNAH5, FARSB, KIF3C | 32 | 33 | cellular assembly and organization, nervous system development, cancer |
ACTA2, DSC2, DSG2, DTX1, DTX3L, MTCL1, NOTCH2, SERPINB12, SRC, TMCO4 | 33 | 33 | cardiac arrhythmia, cardiovascular disease and congenital heart anomaly |
AK7, AK8, AK9, ARC, CAPN6, CAPN8, CAPN9, HIP1, KNTC1, PIPOX | 30 | 33 | nucleic acid and carbohydrate metabolism |
AP5Z1, ASTE1, FLT3, FOXK2, HSP, HSPA2, HSPH1, METAP1, TSC1, PHF3 | 32 | 31 | cell cycle, developmental and hereditary disorders |
aExample of ten molecules present in each network