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 |
---|---|---|---|---|---|
C0155626 | Acute myocardial infarction | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0751956 | Acute Cerebrovascular Accidents | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C1565489 | Renal Insufficiency | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0009402 | Colorectal Carcinoma | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0017636 | Glioblastoma | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0376358 | Malignant neoplasm of prostate | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0008497 | Choriocarcinoma | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0085580 | Essential Hypertension | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0020651 | Hypotension, Orthostatic | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0699790 | Colon Carcinoma | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0745103 | Hyperlipoproteinemia Type IIa | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
C0003864 | Arthritis | OLR1 | 4973 | oxidized low density lipoprotein receptor 1 | P78380 |
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 |
C0008312 | Primary biliary cirrhosis | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0002395 | Alzheimer's Disease | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0034341 | Pyruvate Carboxylase Deficiency Disease | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0015934 | Fetal Growth Retardation | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0027765 | nervous system disorder | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0009402 | Colorectal Carcinoma | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0027651 | Neoplasms | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0018802 | Congestive heart failure | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
C0700095 | Central neuroblastoma | OGDH | 4967 | oxoglutarate dehydrogenase | Q02218 |
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Last updated: August 19, 2024