Table Filtering
Submissions
GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
Glycomics MS Repository for glycan annotations from GlycoWorkbench
All Resources
Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
DisGeNET
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 ▲ |
|---|---|---|---|---|---|
| C0018784 | Sensorineural Hearing Loss (disorder) | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0085580 | Essential Hypertension | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0376359 | Gronblad-Strandberg Syndrome | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0022658 | Kidney Diseases | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0018818 | Ventricular Septal Defects | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0085669 | Acute leukemia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C1561643 | Chronic Kidney Diseases | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0042769 | Virus Diseases | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0026267 | Mitral Valve Prolapse Syndrome | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C1535939 | Pneumocystis jiroveci pneumonia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0002418 | Amblyopia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0030567 | Parkinson Disease | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0020433 | Hyperbilirubinemia | XYLT2 | 64132 | xylosyltransferase 2 | Q9H1B5 |
| C0023890 | Liver Cirrhosis | GLT8D2 | 83468 | glycosyltransferase 8 domain containing 2 | Q9H1C3 |
| C0019196 | Hepatitis C | GLT8D2 | 83468 | glycosyltransferase 8 domain containing 2 | Q9H1C3 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | SLC35B3 | 51000 | solute carrier family 35 member B3 | Q9H1N7 |
| C0024623 | Malignant neoplasm of stomach | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C0027651 | Neoplasms | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C0010674 | Cystic Fibrosis | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C0017205 | Gaucher Disease | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C0699791 | Stomach Carcinoma | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C1961835 | Gaucher Disease, Type 1 | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C0740858 | Substance abuse problem | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
| C0264408 | Childhood asthma | GBA3 | 57733 | glucosylceramidase beta 3 (gene/pseudogene) | Q9H227 |
