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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 | 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 |
| C0524620 | Metabolic Syndrome X | DAG1 | 1605 | dystroglycan 1 | Q14118 |
| C0524620 | Metabolic Syndrome X | GCK | 2645 | glucokinase | P35557 |
| C0524620 | Metabolic Syndrome X | HSPG2 | 3339 | heparan sulfate proteoglycan 2 | P98160 |
| C0524620 | Metabolic Syndrome X | PCK1 | 5105 | phosphoenolpyruvate carboxykinase 1 | P35558 |
| C0524620 | Metabolic Syndrome X | ACOX1 | 51 | acyl-CoA oxidase 1 | Q15067 |
| C0524620 | Metabolic Syndrome X | PCK2 | 5106 | phosphoenolpyruvate carboxykinase 2, mitochondrial | Q16822 |
| C0524620 | Metabolic Syndrome X | PIK3CA | 5290 | phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | P42336 |
| C0524620 | Metabolic Syndrome X | PLA2G4A | 5321 | phospholipase A2 group IVA | P47712 |
| C0524620 | Metabolic Syndrome X | RENBP | 5973 | renin binding protein | P51606 |
| C0524620 | Metabolic Syndrome X | AKR1C3 | 8644 | aldo-keto reductase family 1 member C3 | P42330 |
| C0524620 | Metabolic Syndrome X | CDH13 | 1012 | cadherin 13 | P55290 |
| C0524620 | Metabolic Syndrome X | ACSM1 | 116285 | acyl-CoA synthetase medium chain family member 1 | Q08AH1 |
| C0524620 | Metabolic Syndrome X | SLC27A5 | 10998 | solute carrier family 27 member 5 | Q9Y2P5 |
