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 |
---|---|---|---|---|---|
C0036457 | Scrapie | PRNP | 5621 | prion protein | P04156 |
C1568272 | Tendinopathy | PRNP | 5621 | prion protein | P04156 |
C0282513 | Primary Progressive Aphasia (disorder) | PRNP | 5621 | prion protein | P04156 |
C0014038 | Encephalitis | PRNP | 5621 | prion protein | P04156 |
C1263846 | Attention deficit hyperactivity disorder | PRNP | 5621 | prion protein | P04156 |
C0027066 | Myoclonus | PRNP | 5621 | prion protein | P04156 |
C0409959 | Osteoarthritis, Knee | PRNP | 5621 | prion protein | P04156 |
C0752125 | Spinocerebellar Ataxia Type 7 | PRNP | 5621 | prion protein | P04156 |
C0005129 | Bernard-Soulier Syndrome | PRNP | 5621 | prion protein | P04156 |
C0036341 | Schizophrenia | PRNP | 5621 | prion protein | P04156 |
C0030567 | Parkinson Disease | PRNP | 5621 | prion protein | P04156 |
C0949664 | Tauopathies | PRNP | 5621 | prion protein | P04156 |
C0752347 | Lewy Body Disease | PRNP | 5621 | prion protein | P04156 |
C0014556 | Epilepsy, Temporal Lobe | PRNP | 5621 | prion protein | P04156 |
C0024790 | Paroxysmal nocturnal hemoglobinuria | PRNP | 5621 | prion protein | P04156 |
C0026848 | Myopathy | PRNP | 5621 | prion protein | P04156 |
C3665347 | Visual Impairment | PRNP | 5621 | prion protein | P04156 |
C0393547 | Bulbospinal Neuronopathy | PRNP | 5621 | prion protein | P04156 |
C0036572 | Seizures | PRNP | 5621 | prion protein | P04156 |
C0011884 | Diabetic Retinopathy | PRNP | 5621 | prion protein | P04156 |
C0040997 | Trigeminal Neuralgia | PRNP | 5621 | prion protein | P04156 |
C0028841 | Ocular Hypotension | PRNP | 5621 | prion protein | P04156 |
C3495559 | Juvenile arthritis | PRNP | 5621 | prion protein | P04156 |
C0021400 | Influenza | PRNP | 5621 | prion protein | P04156 |
C0007760 | Cerebellar Diseases | PRNP | 5621 | prion protein | P04156 |
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Last updated: August 19, 2024