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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 | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
| C0524620 | Metabolic Syndrome X | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
| C0524620 | Metabolic Syndrome X | CANX | 821 | calnexin | P27824 |
| C0524620 | Metabolic Syndrome X | CALR | 811 | calreticulin | P27797 |
| C0524620 | Metabolic Syndrome X | KL | 9365 | klotho | Q9UEF7 |
| C0524620 | Metabolic Syndrome X | CD38 | 952 | CD38 molecule | P28907 |
| C0524620 | Metabolic Syndrome X | H6PD | 9563 | hexose-6-phosphate dehydrogenase/glucose 1-dehydrogenase | O95479 |
| C0524620 | Metabolic Syndrome X | SDC3 | 9672 | syndecan 3 | O75056 |
| C0524620 | Metabolic Syndrome X | CYP46A1 | 10858 | cytochrome P450 family 46 subfamily A member 1 | Q9Y6A2 |
| C0524620 | Metabolic Syndrome X | CHGA | 1113 | chromogranin A | P10645 |
| C0524620 | Metabolic Syndrome X | MGLL | 11343 | monoglyceride lipase | Q99685 |
| C0524620 | Metabolic Syndrome X | CYP2R1 | 120227 | cytochrome P450 family 2 subfamily R member 1 | Q6VVX0 |
| C0524620 | Metabolic Syndrome X | CYP3A5 | 1577 | cytochrome P450 family 3 subfamily A member 5 | P20815 |
| C0524620 | Metabolic Syndrome X | CYP17A1 | 1586 | cytochrome P450 family 17 subfamily A member 1 | P05093 |
| C0524620 | Metabolic Syndrome X | ACE | 1636 | angiotensin I converting enzyme | P12821 |
| C0524620 | Metabolic Syndrome X | ALDH2 | 217 | aldehyde dehydrogenase 2 family member | P05091 |
| C0524620 | Metabolic Syndrome X | ACSL4 | 2182 | acyl-CoA synthetase long chain family member 4 | O60488 |
| C0524620 | Metabolic Syndrome X | PLCB1 | 23236 | phospholipase C beta 1 | Q9NQ66 |
| C0524620 | Metabolic Syndrome X | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
| C0524620 | Metabolic Syndrome X | GGT1 | 2678 | gamma-glutamyltransferase 1 | P19440 |
| C0524620 | Metabolic Syndrome X | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0524620 | Metabolic Syndrome X | MCAT | 27349 | malonyl-CoA-acyl carrier protein transacylase | Q8IVS2 |
| C0524620 | Metabolic Syndrome X | GPX1 | 2876 | glutathione peroxidase 1 | P07203 |
| C0524620 | Metabolic Syndrome X | HSD11B1 | 3290 | hydroxysteroid 11-beta dehydrogenase 1 | P28845 |
| C0524620 | Metabolic Syndrome X | ACACB | 32 | acetyl-CoA carboxylase beta | O00763 |
