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 |
---|---|---|---|---|---|
C0684249 | Carcinoma of lung | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0393819 | Polyradiculoneuropathy, Chronic Inflammatory Demyelinating | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0029438 | Massive Osteolyses | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0026769 | Multiple Sclerosis | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0242379 | Malignant neoplasm of lung | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C1854678 | MULTIPLE PTERYGIUM SYNDROME, LETHAL TYPE | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0020224 | Polyhydramnios | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0919267 | ovarian neoplasm | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0342790 | Carnitine palmitoyl transferase 2 deficiency | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C1276035 | Pena-Shokeir syndrome type I | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0023520 | Leukodystrophy | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0497327 | Dementia | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0037299 | Skin Ulcer | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0270790 | Quadriparesis | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0025517 | Metabolic Diseases | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0270960 | Congenital myopathy (disorder) | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0265261 | Multiple pterygium syndrome | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C1856304 | GSD IV, Neuromuscular Form, Congenital | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0023467 | Leukemia, Myelocytic, Acute | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0152013 | Adenocarcinoma of lung (disorder) | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0017495 | Gerstmann-Straussler-Scheinker Disease | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0025202 | melanoma | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C1969443 | Trifunctional Protein Deficiency With Myopathy And Neuropathy | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0878544 | Cardiomyopathies | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
C0017921 | Glycogen storage disease type II | GBE1 | 2632 | 1,4-alpha-glucan branching enzyme 1 | Q04446 |
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Last updated: August 19, 2024