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 |
---|---|---|---|---|---|
C1956346 | Coronary Artery Disease | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0600139 | Prostate carcinoma | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0028738 | Nystagmus | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0025202 | melanoma | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0020490 | Hyperopia | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0011303 | Demyelinating Diseases | MAG | 4099 | myelin associated glycoprotein | P20916 |
C1510429 | Entrapment Neuropathies | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0004364 | Autoimmune Diseases | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0032587 | Polyradiculoneuropathy | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0700095 | Central neuroblastoma | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0205711 | Pelizaeus-Merzbacher Disease | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0376358 | Malignant neoplasm of prostate | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0007785 | Cerebral Infarction | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0027765 | nervous system disorder | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0740392 | Infarction, Middle Cerebral Artery | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0393819 | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0027051 | Myocardial Infarction | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0028754 | Obesity | MIOX | 55586 | myo-inositol oxygenase | Q9UGB7 |
C0032460 | Polycystic Ovary Syndrome | MIOX | 55586 | myo-inositol oxygenase | Q9UGB7 |
C0011847 | Diabetes | MIOX | 55586 | myo-inositol oxygenase | Q9UGB7 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | MIOX | 55586 | myo-inositol oxygenase | Q9UGB7 |
C0011849 | Diabetes Mellitus | MIOX | 55586 | myo-inositol oxygenase | Q9UGB7 |
C0010414 | Infection by Cryptococcus neoformans | MIOX | 55586 | myo-inositol oxygenase | Q9UGB7 |
C0015695 | Fatty Liver | MIOX | 55586 | myo-inositol oxygenase | Q9UGB7 |
C0036572 | Seizures | MYORG | 57462 | myogenesis regulating glycosidase (putative) | Q6NSJ0 |
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Last updated: August 19, 2024