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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 ▲ |
|---|---|---|---|---|---|
| C0026769 | Multiple Sclerosis | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C0520680 | Sleep Apnea, Central | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C0917805 | Transient Cerebral Ischemia | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C0029463 | Osteosarcoma | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
| C1857276 | Trichohepatoenteric Syndrome | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0011991 | Diarrhea | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0023530 | Leukopenia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0699790 | Colon Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0007102 | Malignant tumor of colon | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0006142 | Malignant neoplasm of breast | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C3806688 | Solute carrier family 35 member A2 congenital disorder of glycosylation | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0010324 | Crigler Najjar syndrome, type 1 | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0027651 | Neoplasms | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0010414 | Infection by Cryptococcus neoformans | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0017551 | Gilbert Disease (disorder) | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0027947 | Neutropenia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0268138 | Xeroderma Pigmentosum, Complementation Group D | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0008350 | Cholelithiasis | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0520679 | Sleep Apnea, Obstructive | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0006826 | Malignant Neoplasms | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0009402 | Colorectal Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0014544 | Epilepsy | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0039685 | Tetralogy of Fallot | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0007097 | Carcinoma | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
| C0020433 | Hyperbilirubinemia | SLC35A2 | 7355 | solute carrier family 35 member A2 | P78381 |
