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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 |
|---|---|---|---|---|---|
| C0004943 | Behcet Syndrome | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C0004943 | Behcet Syndrome | KLRC1 | 3821 | killer cell lectin like receptor C1 | P26715 |
| C0004943 | Behcet Syndrome | LGALS3 | 3958 | galectin 3 | P17931 |
| C0004943 | Behcet Syndrome | MBL2 | 4153 | mannose binding lectin 2 | P11226 |
| C0004943 | Behcet Syndrome | MRC1 | 4360 | mannose receptor C-type 1 | P22897 |
| C0004943 | Behcet Syndrome | PLA2G2A | 5320 | phospholipase A2 group IIA | P14555 |
| C0004943 | Behcet Syndrome | CNTN5 | 53942 | contactin 5 | O94779 |
| C0004943 | Behcet Syndrome | SELL | 6402 | selectin L | P14151 |
| C0004943 | Behcet Syndrome | SELE | 6401 | selectin E | P16581 |
| C0004943 | Behcet Syndrome | CLEC7A | 64581 | C-type lectin domain containing 7A | Q9BXN2 |
| C0004943 | Behcet Syndrome | VCAM1 | 7412 | vascular cell adhesion molecule 1 | P19320 |
| C0004943 | Behcet Syndrome | PLA2G6 | 8398 | phospholipase A2 group VI | O60733 |
| C0004943 | Behcet Syndrome | CAT | 847 | catalase | P04040 |
| C0004943 | Behcet Syndrome | CD14 | 929 | CD14 molecule | P08571 |
| C0004943 | Behcet Syndrome | TPI1 | 7167 | triosephosphate isomerase 1 | P60174 |
| C0004943 | Behcet Syndrome | MICA | 100507436 | MHC class I polypeptide-related sequence A | Q29983 |
| C0004943 | Behcet Syndrome | CYP2B6 | 1555 | cytochrome P450 family 2 subfamily B member 6 | P20813 |
| C0004943 | Behcet Syndrome | CYP2C19 | 1557 | cytochrome P450 family 2 subfamily C member 19 | P33261 |
| C0004943 | Behcet Syndrome | CYP2C9 | 1559 | cytochrome P450 family 2 subfamily C member 9 | P11712 |
| C0004943 | Behcet Syndrome | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
| C0004943 | Behcet Syndrome | CLEC16A | 23274 | C-type lectin domain containing 16A | Q2KHT3 |
| C0004943 | Behcet Syndrome | FCN2 | 2220 | ficolin 2 | Q15485 |
| C0004943 | Behcet Syndrome | KLRD1 | 3824 | killer cell lectin like receptor D1 | Q13241 |
| C0004943 | Behcet Syndrome | ACLY | 47 | ATP citrate lyase | P53396 |
| C0004943 | Behcet Syndrome | PAFAH1B1 | 5048 | platelet activating factor acetylhydrolase 1b regulatory subunit 1 | P43034 |
