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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 | UGT1A6 | 54578 | UDP glucuronosyltransferase family 1 member A6 | P19224 |
| C0524620 | Metabolic Syndrome X | UGT1A10 | 54575 | UDP glucuronosyltransferase family 1 member A10 | Q9HAW8 |
| C0524620 | Metabolic Syndrome X | UGT1A5 | 54579 | UDP glucuronosyltransferase family 1 member A5 | P35504 |
| C0524620 | Metabolic Syndrome X | UGT1A1 | 54658 | UDP glucuronosyltransferase family 1 member A1 | P22309 |
| C0524620 | Metabolic Syndrome X | UGT1A4 | 54657 | UDP glucuronosyltransferase family 1 member A4 | P22310 |
| C0524620 | Metabolic Syndrome X | UGT1A9 | 54600 | UDP glucuronosyltransferase family 1 member A9 | O60656 |
| C0524620 | Metabolic Syndrome X | UGT1A3 | 54659 | UDP glucuronosyltransferase family 1 member A3 | P35503 |
| C0524620 | Metabolic Syndrome X | G6PC2 | 57818 | glucose-6-phosphatase catalytic subunit 2 | Q9NQR9 |
| 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 |
