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 |
---|---|---|---|---|---|
C0442874 | Neuropathy | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0036341 | Schizophrenia | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0037772 | Spastic Paraplegia | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0006826 | Malignant Neoplasms | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0007959 | Charcot-Marie-Tooth Disease | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0002395 | Alzheimer's Disease | MAG | 4099 | myelin associated glycoprotein | P20916 |
C4225250 | SPASTIC PARAPLEGIA 75, AUTOSOMAL RECESSIVE | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0344315 | Depressed mood | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0007758 | Cerebellar Ataxia | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0027743 | Nerve compression syndrome | MAG | 4099 | myelin associated glycoprotein | P20916 |
C4721453 | Peripheral Nervous System Diseases | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0027819 | Neuroblastoma | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0026769 | Multiple Sclerosis | MAG | 4099 | myelin associated glycoprotein | P20916 |
C4082197 | Charcot-Marie-Tooth disease type 4 | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0340803 | Capillary malformation (disorder) | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0026470 | Monoclonal Gammopathy of Undetermined Significance | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0030297 | Pancreatic Neoplasm | MAG | 4099 | myelin associated glycoprotein | P20916 |
C1858723 | Poikiloderma with Neutropenia | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0023520 | Leukodystrophy | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0018916 | Hemangioma | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0030567 | Parkinson Disease | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0752347 | Lewy Body Disease | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0029124 | Optic Atrophy | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0031117 | Peripheral Neuropathy | MAG | 4099 | myelin associated glycoprotein | P20916 |
C0029134 | Optic Neuritis | MAG | 4099 | myelin associated glycoprotein | P20916 |
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Last updated: August 19, 2024