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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 | 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 |
| C0524620 | Metabolic Syndrome X | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0524620 | Metabolic Syndrome X | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0524620 | Metabolic Syndrome X | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
| C0524620 | Metabolic Syndrome X | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
| C0524620 | Metabolic Syndrome X | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
| C0524620 | Metabolic Syndrome X | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
| C0524620 | Metabolic Syndrome X | EPHX2 | 2053 | epoxide hydrolase 2 | P34913 |
| C0524620 | Metabolic Syndrome X | ACSL1 | 2180 | acyl-CoA synthetase long chain family member 1 | P33121 |
| C0524620 | Metabolic Syndrome X | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0524620 | Metabolic Syndrome X | LPIN1 | 23175 | lipin 1 | Q14693 |
| C0524620 | Metabolic Syndrome X | ALOX5 | 240 | arachidonate 5-lipoxygenase | P09917 |
| C0524620 | Metabolic Syndrome X | NAAA | 27163 | N-acylethanolamine acid amidase | Q02083 |
| C0524620 | Metabolic Syndrome X | GPX3 | 2878 | glutathione peroxidase 3 | P22352 |
| C0524620 | Metabolic Syndrome X | HSD11B2 | 3291 | hydroxysteroid 11-beta dehydrogenase 2 | P80365 |
| C0524620 | Metabolic Syndrome X | ACACA | 31 | acetyl-CoA carboxylase alpha | Q13085 |
| C0524620 | Metabolic Syndrome X | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
| C0524620 | Metabolic Syndrome X | ACADVL | 37 | acyl-CoA dehydrogenase very long chain | P49748 |
| C0524620 | Metabolic Syndrome X | SLC35D3 | 340146 | solute carrier family 35 member D3 | Q5M8T2 |
| C0524620 | Metabolic Syndrome X | LTC4S | 4056 | leukotriene C4 synthase | Q16873 |
| C0524620 | Metabolic Syndrome X | MTM1 | 4534 | myotubularin 1 | Q13496 |
