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DisGeNET
DisGeNET is a knowledge management platform that integrates and standardizes the data of genes and mutations related to diseases from multiple sources. It covers entire range of human disease.
| Source | Last Updated |
|---|---|
| DisGeNET | July 29, 2024 |
| Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
|---|---|---|---|---|---|
| C0524620 | Metabolic Syndrome X | PNPLA2 | 57104 | patatin like phospholipase domain containing 2 | Q96AD5 |
| C0524620 | Metabolic Syndrome X | ACSM3 | 6296 | acyl-CoA synthetase medium chain family member 3 | Q53FZ2 |
| C0524620 | Metabolic Syndrome X | SCD | 6319 | stearoyl-CoA desaturase | O00767 |
| C0524620 | Metabolic Syndrome X | SELE | 6401 | selectin E | P16581 |
| C0524620 | Metabolic Syndrome X | SELP | 6403 | selectin P | P16109 |
| C0524620 | Metabolic Syndrome X | SLC2A2 | 6514 | solute carrier family 2 member 2 | P11168 |
| C0524620 | Metabolic Syndrome X | SLC2A5 | 6518 | solute carrier family 2 member 5 | P22732 |
| C0524620 | Metabolic Syndrome X | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
| C0524620 | Metabolic Syndrome X | SLC5A1 | 6523 | solute carrier family 5 member 1 | P13866 |
| C0524620 | Metabolic Syndrome X | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
| C0524620 | Metabolic Syndrome X | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
| C0524620 | Metabolic Syndrome X | UMOD | 7369 | uromodulin | P07911 |
| C0524620 | Metabolic Syndrome X | PTGES2 | 80142 | prostaglandin E synthase 2 | Q9H7Z7 |
| C0524620 | Metabolic Syndrome X | MBOAT7 | 79143 | membrane bound O-acyltransferase domain containing 7 | Q96N66 |
| C0524620 | Metabolic Syndrome X | PNPLA3 | 80339 | patatin like phospholipase domain containing 3 | Q9NST1 |
| C0524620 | Metabolic Syndrome X | COLEC12 | 81035 | collectin subfamily member 12 | Q5KU26 |
| C0524620 | Metabolic Syndrome X | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0524620 | Metabolic Syndrome X | CAT | 847 | catalase | P04040 |
| C0524620 | Metabolic Syndrome X | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0524620 | Metabolic Syndrome X | CD14 | 929 | CD14 molecule | P08571 |
| C0524620 | Metabolic Syndrome X | LIPG | 9388 | lipase G, endothelial type | Q9Y5X9 |
| C0524620 | Metabolic Syndrome X | FADS2 | 9415 | fatty acid desaturase 2 | O95864 |
| C0524620 | Metabolic Syndrome X | NAMPT | 10135 | nicotinamide phosphoribosyltransferase | P43490 |
| C0524620 | Metabolic Syndrome X | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0524620 | Metabolic Syndrome X | CPT1A | 1374 | carnitine palmitoyltransferase 1A | P50416 |
