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 |
---|---|---|---|---|---|
C0004096 | Asthma | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C0002395 | Alzheimer's Disease | GNPDA2 | 132789 | glucosamine-6-phosphate deaminase 2 | Q8TDQ7 |
C0684276 | Hypsarrhythmia | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0751748 | Nonketotic Hyperglycinemia | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0036572 | Seizures | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0426970 | Spastic Quadriplegia | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0025958 | Microcephaly | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0027066 | Myoclonus | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0268165 | Primary hyperoxaluria type 2 | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0085584 | Encephalopathies | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0220981 | Metabolic acidosis | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C3714756 | Intellectual Disability | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0036341 | Schizophrenia | GLYCTK | 132158 | glycerate kinase | Q8IVS8 |
C0006826 | Malignant Neoplasms | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
C0027651 | Neoplasms | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
C1306459 | Primary malignant neoplasm | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
C0684249 | Carcinoma of lung | CRYBG3 | 131544 | crystallin beta-gamma domain containing 3 | Q68DQ2 |
C0002395 | Alzheimer's Disease | LYZL4 | 131375 | lysozyme like 4 | Q96KX0 |
C0023903 | Liver neoplasms | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1852197 | MAJOR AFFECTIVE DISORDER 1 | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0003469 | Anxiety Disorders | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0006142 | Malignant neoplasm of breast | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C1321551 | Shprintzen-Goldberg syndrome | COMT | 1312 | catechol-O-methyltransferase | P21964 |
C0030319 | Panic Disorder | COMT | 1312 | catechol-O-methyltransferase | P21964 |
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Last updated: August 19, 2024