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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 |
|---|---|---|---|---|---|
| C0020538 | Hypertensive disease | RGN | 9104 | regucalcin | Q15493 |
| C0020538 | Hypertensive disease | MSLN | 10232 | mesothelin | Q13421 |
| C0020538 | Hypertensive disease | EBP | 10682 | EBP cholestenol delta-isomerase | Q15125 |
| C0020538 | Hypertensive disease | CLC | 1178 | Charcot-Leyden crystal galectin | Q05315 |
| C0020538 | Hypertensive disease | COL9A2 | 1298 | collagen type IX alpha 2 chain | Q14055 |
| C0020538 | Hypertensive disease | CYP1B1 | 1545 | cytochrome P450 family 1 subfamily B member 1 | Q16678 |
| C0020538 | Hypertensive disease | SLC35F3 | 148641 | solute carrier family 35 member F3 | Q8IY50 |
| C0020538 | Hypertensive disease | REG3G | 130120 | regenerating family member 3 gamma | Q6UW15 |
| C0020538 | Hypertensive disease | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
| C0020538 | Hypertensive disease | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0020538 | Hypertensive disease | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0020538 | Hypertensive disease | CYP2C8 | 1558 | cytochrome P450 family 2 subfamily C member 8 | P10632 |
| C0020538 | Hypertensive disease | CYP4A11 | 1579 | cytochrome P450 family 4 subfamily A member 11 | Q02928 |
| C0020538 | Hypertensive disease | CYP3A4 | 1576 | cytochrome P450 family 3 subfamily A member 4 | P08684 |
| C0020538 | Hypertensive disease | CYP7A1 | 1581 | cytochrome P450 family 7 subfamily A member 1 | P22680 |
| C0020538 | Hypertensive disease | CYP2J2 | 1573 | cytochrome P450 family 2 subfamily J member 2 | P51589 |
| C0020538 | Hypertensive disease | CYP11B2 | 1585 | cytochrome P450 family 11 subfamily B member 2 | P19099 |
| C0020538 | Hypertensive disease | CYP19A1 | 1588 | cytochrome P450 family 19 subfamily A member 1 | P11511 |
| C0020538 | Hypertensive disease | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
| C0020538 | Hypertensive disease | CYP11B1 | 1584 | cytochrome P450 family 11 subfamily B member 1 | P15538 |
| C0020538 | Hypertensive disease | CYP21A2 | 1589 | cytochrome P450 family 21 subfamily A member 2 | P08686 |
| C0020538 | Hypertensive disease | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
| C0020538 | Hypertensive disease | EPHX2 | 2053 | epoxide hydrolase 2 | P34913 |
| C0020538 | Hypertensive disease | ABAT | 18 | 4-aminobutyrate aminotransferase | P80404 |
| C0020538 | Hypertensive disease | AGXT | 189 | alanine--glyoxylate and serine--pyruvate aminotransferase | P21549 |
