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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 |
|---|---|---|---|---|---|
| C0004997 | Benign Ovarian Neoplasm | SLC2A3 | 6515 | solute carrier family 2 member 3 | P11169 |
| C0004997 | Benign Ovarian Neoplasm | SLC2A4 | 6517 | solute carrier family 2 member 4 | P14672 |
| C0004997 | Benign Ovarian Neoplasm | OPCML | 4978 | opioid binding protein/cell adhesion molecule like | Q14982 |
| C0281784 | Benign Meningioma | LGALS3 | 3958 | galectin 3 | P17931 |
| C0281784 | Benign Meningioma | FASN | 2194 | fatty acid synthase | P49327 |
| C0281784 | Benign Meningioma | PTEN | 5728 | phosphatase and tensin homolog | P60484 |
| C2242987 | Benign Mastocytoma | HS2ST1 | 9653 | heparan sulfate 2-O-sulfotransferase 1 | Q7LGA3 |
| C2242987 | Benign Mastocytoma | PLA2G2E | 30814 | phospholipase A2 group IIE | Q9NZK7 |
| C2242987 | Benign Mastocytoma | ICAM1 | 3383 | intercellular adhesion molecule 1 | P05362 |
| C0393584 | Benign Hereditary Chorea | CACNA2D2 | 9254 | calcium voltage-gated channel auxiliary subunit alpha2delta 2 | Q9NY47 |
| C0376175 | Bell Palsy | SMUG1 | 23583 | single-strand-selective monofunctional uracil-DNA glycosylase 1 | Q53HV7 |
| C0376175 | Bell Palsy | HPGDS | 27306 | hematopoietic prostaglandin D synthase | O60760 |
| C0004943 | Behcet Syndrome | SLC35A1 | 10559 | solute carrier family 35 member A1 | P78382 |
| C0004943 | Behcet Syndrome | FUT2 | 2524 | fucosyltransferase 2 | Q10981 |
| C0004943 | Behcet Syndrome | GAL3ST1 | 9514 | galactose-3-O-sulfotransferase 1 | Q99999 |
| C0004943 | Behcet Syndrome | GLB1 | 2720 | galactosidase beta 1 | P16278 |
| C0004943 | Behcet Syndrome | ARSA | 410 | arylsulfatase A | P15289 |
| C0004943 | Behcet Syndrome | ENO1 | 2023 | enolase 1 | P06733 |
| C0004943 | Behcet Syndrome | IL1R1 | 3554 | interleukin 1 receptor type 1 | P14778 |
| C0004943 | Behcet Syndrome | LYZ | 4069 | lysozyme | P61626 |
| C0004943 | Behcet Syndrome | CALR | 811 | calreticulin | P27797 |
| C0004943 | Behcet Syndrome | NEIL1 | 79661 | nei like DNA glycosylase 1 | Q96FI4 |
| C0004943 | Behcet Syndrome | PRSS21 | 10942 | serine protease 21 | Q9Y6M0 |
| C0004943 | Behcet Syndrome | CYP1A1 | 1543 | cytochrome P450 family 1 subfamily A member 1 | P04798 |
| C0004943 | Behcet Syndrome | CYP27B1 | 1594 | cytochrome P450 family 27 subfamily B member 1 | O15528 |
