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 |
---|---|---|---|---|---|
C2239176 | Liver carcinoma | AGPS | 8540 | alkylglycerone phosphate synthase | O00116 |
C0162824 | Dermatitis, Photoallergic | AGPS | 8540 | alkylglycerone phosphate synthase | O00116 |
C0017638 | Glioma | AGPS | 8540 | alkylglycerone phosphate synthase | O00116 |
C0549473 | Thyroid carcinoma | AGPS | 8540 | alkylglycerone phosphate synthase | O00116 |
C0040136 | Thyroid Neoplasm | AGPS | 8540 | alkylglycerone phosphate synthase | O00116 |
C3808739 | MYASTHENIC SYNDROME, CONGENITAL, 8 | AGRN | 375790 | agrin | O00468 |
C0023467 | Leukemia, Myelocytic, Acute | AGRN | 375790 | agrin | O00468 |
C0152013 | Adenocarcinoma of lung (disorder) | AGRN | 375790 | agrin | O00468 |
C0028738 | Nystagmus | AGRN | 375790 | agrin | O00468 |
C0238463 | Papillary thyroid carcinoma | AGRN | 375790 | agrin | O00468 |
C0036572 | Seizures | AGRN | 375790 | agrin | O00468 |
C0018784 | Sensorineural Hearing Loss (disorder) | AGRN | 375790 | agrin | O00468 |
C0751883 | Congenital Myasthenic Syndromes, Postsynaptic | AGRN | 375790 | agrin | O00468 |
C0751882 | Myasthenic Syndromes, Congenital | AGRN | 375790 | agrin | O00468 |
C0002395 | Alzheimer's Disease | AGRN | 375790 | agrin | O00468 |
C0026998 | Acute Myeloid Leukemia, M1 | AGRN | 375790 | agrin | O00468 |
C0014877 | Esotropia | AGRN | 375790 | agrin | O00468 |
C1306459 | Primary malignant neoplasm | AGRN | 375790 | agrin | O00468 |
C0520680 | Sleep Apnea, Central | AGRN | 375790 | agrin | O00468 |
C0017168 | Gastroesophageal reflux disease | AGRN | 375790 | agrin | O00468 |
C1276035 | Pena-Shokeir syndrome type I | AGRN | 375790 | agrin | O00468 |
C0751885 | Myasthenic Syndromes, Congenital, Slow Channel | AGRN | 375790 | agrin | O00468 |
C0751884 | Congenital Myasthenic Syndromes, Presynaptic | AGRN | 375790 | agrin | O00468 |
C4082299 | Bulbar palsy | AGRN | 375790 | agrin | O00468 |
C0029089 | Ophthalmoplegia | AGRN | 375790 | agrin | O00468 |
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Last updated: August 19, 2024