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 |
---|---|---|---|---|---|
C0014868 | Esophagitis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0344530 | Congenital keratoglobus | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C4707243 | Familial thoracic aortic aneurysm and aortic dissection | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0017168 | Gastroesophageal reflux disease | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0600228 | Cardiopulmonary Arrest | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0019294 | Hernia, Inguinal | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0206062 | Lung Diseases, Interstitial | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C1855179 | CATARACT, ANTERIOR POLAR | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0948008 | Ischemic stroke | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0018790 | Cardiac Arrest | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0010278 | Craniosynostosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C2697932 | Loeys-Dietz Syndrome | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0003507 | Aortic Valve Stenosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0398738 | Leukocyte adhesion deficiency type 1 | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0009782 | Connective Tissue Diseases | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C1458155 | Mammary Neoplasms | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0027059 | Myocarditis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0007194 | Hypertrophic Cardiomyopathy | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0600260 | Lung Diseases, Obstructive | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0034194 | Pyloric Stenosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0003486 | Aortic Aneurysm | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C1306503 | Congenital exomphalos | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0085096 | Peripheral Vascular Diseases | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0038379 | Strabismus | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
C0005744 | Blepharophimosis | SLC2A10 | 81031 | solute carrier family 2 member 10 | O95528 |
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Last updated: August 19, 2024