Supplementary Table 6.
Possible T2D causing genes that are both highly represented in our analysis within the gold-standard pathways of T2D and also found in DisGeNET as associated with T2D.
| ABCC8 | ADRB3 | CACNA1D | EPO | HNF4A | IRS2 | NPY | PPARA | SLC2A4 |
| ACACA | AGTR1 | CAMKK2 | ERBB4 | HSD17B12 | KCNJ11 | NR1D1 | PPARD | SOCS3 |
| ACACB | AKT1 | CCND2 | FADS2 | IL10 | LEPR | NR1H3 | PPARG | SORBS1 |
| ACSL1 | AKT2 | CDKN2A | FASN | IL23R | LPL | ONECUT1 | PPARGC1A | SREBF1 |
| ADCY3 | AKT3 | CDKN2B | FOXO1 | IL4R | MCM6 | PCK1 | PPP1R3A | TACR3 |
| ADIPOQ | ALDH2 | CHEK2 | GCK | IL6 | NEUROD1 | PDX1 | PRKAA2 | TCF7L2 |
| ADIPOR1 | ALDH7A1 | CHRM3 | GYS1 | IL6R | NEUROG3 | PIK3CB | PTPN1 | TGFB1 |
| ADIPOR2 | ARNTL | CLOCK | HK2 | INS | NFKB1 | PKLR | RAPGEF1 | TNF |
| ADRA1A | BCAT1 | CRY2 | HNF1A | INSR | NOS3 | PLIN1 | SLC2A1 | TP53 |
| ADRB2 | BRAF | CTBP1 | HNF1B | IRS1 | NOTCH2 | PLTP | SLC2A2 | WNT5B |