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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 |
|---|---|---|---|---|---|
| C0019163 | Hepatitis B | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
| C3150651 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 2 | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
| C2750440 | FATTY LIVER DISEASE, NONALCOHOLIC, SUSCEPTIBILITY TO, 1 | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
| C0376358 | Malignant neoplasm of prostate | DGAT2 | 84649 | diacylglycerol O-acyltransferase 2 | Q96PD7 |
| C0086445 | Idiopathic Membranous Glomerulonephritis | PLA2G12B | 84647 | phospholipase A2 group XIIB | Q9BX93 |
| C0006142 | Malignant neoplasm of breast | ST6GAL2 | 84620 | ST6 beta-galactoside alpha-2,6-sialyltransferase 2 | Q96JF0 |
| C0014859 | Esophageal Neoplasms | ST6GAL2 | 84620 | ST6 beta-galactoside alpha-2,6-sialyltransferase 2 | Q96JF0 |
| C0206682 | Follicular thyroid carcinoma | ST6GAL2 | 84620 | ST6 beta-galactoside alpha-2,6-sialyltransferase 2 | Q96JF0 |
| C0684249 | Carcinoma of lung | TPST1 | 8460 | tyrosylprotein sulfotransferase 1 | O60507 |
| C0009402 | Colorectal Carcinoma | TPST1 | 8460 | tyrosylprotein sulfotransferase 1 | O60507 |
| C0242379 | Malignant neoplasm of lung | TPST1 | 8460 | tyrosylprotein sulfotransferase 1 | O60507 |
| C0003868 | Arthritis, Gouty | TPST1 | 8460 | tyrosylprotein sulfotransferase 1 | O60507 |
| C0027651 | Neoplasms | TPST1 | 8460 | tyrosylprotein sulfotransferase 1 | O60507 |
| C1854896 | Mucolipidosis III Gamma | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0085078 | Lysosomal Storage Diseases | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0036439 | Scoliosis, unspecified | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0038506 | Stuttering | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0026697 | Mucolipidoses | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0033788 | Pseudo-Hurler Polydystrophy | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0003504 | Aortic Valve Insufficiency | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0027092 | Myopia | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0020725 | Type II Mucolipidosis | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0026707 | Mucopolysaccharidosis IV | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0013336 | Dwarfism | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
| C0035334 | Retinitis Pigmentosa | GNPTG | 84572 | N-acetylglucosamine-1-phosphate transferase subunit gamma | Q9UJJ9 |
