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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol ▼ | Gene ID | Gene Name | UniProt ID |
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C3489413 | Lipomatosis, Multiple | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0243026 | Sepsis | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0008370 | Cholestasis | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0025517 | Metabolic Diseases | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0206692 | Carcinoma, Lobular | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0006142 | Malignant neoplasm of breast | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0686353 | Muscular Dystrophies, Limb-Girdle | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0242363 | Islet Cell Tumor | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0017926 | Glycogen Storage Disease Type VII | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0241005 | Creatine phosphokinase serum increased | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0151744 | Myocardial Ischemia | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0032914 | Pre-Eclampsia | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0027080 | Myoglobinuria | PYGM | 5837 | glycogen phosphorylase, muscle associated | P11217 |
C0017925 | Glycogen Storage Disease Type VI | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C2239176 | Liver carcinoma | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0017495 | Gerstmann-Straussler-Scheinker Disease | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0017920 | Glycogen Storage Disease Type I | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0020615 | Hypoglycemia | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0017924 | Glycogen Storage Disease Type V | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0013336 | Dwarfism | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0029438 | Massive Osteolyses | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0017922 | Glycogen Storage Disease Type III | PYGL | 5836 | glycogen phosphorylase L | P06737 |
C0155626 | Acute myocardial infarction | PYGB | 5834 | glycogen phosphorylase B | P11216 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | PYGB | 5834 | glycogen phosphorylase B | P11216 |
C0151744 | Myocardial Ischemia | PYGB | 5834 | glycogen phosphorylase B | P11216 |
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Last updated: August 19, 2024