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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 |
|---|---|---|---|---|---|
| C0030305 | Pancreatitis | QTRT1 | 81890 | queuine tRNA-ribosyltransferase catalytic subunit 1 | Q9BXR0 |
| C0002395 | Alzheimer's Disease | HYI | 81888 | hydroxypyruvate isomerase (putative) | Q5T013 |
| C0003873 | Rheumatoid Arthritis | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C1956346 | Coronary Artery Disease | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0010054 | Coronary Arteriosclerosis | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0006826 | Malignant Neoplasms | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0027651 | Neoplasms | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0007867 | Cervix Diseases | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0024299 | Lymphoma | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0006142 | Malignant neoplasm of breast | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0010068 | Coronary heart disease | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C1306459 | Primary malignant neoplasm | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0017638 | Glioma | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0007847 | Malignant tumor of cervix | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0206708 | Cervical Intraepithelial Neoplasia | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0302592 | Cervix carcinoma | ST6GALNAC5 | 81849 | ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 5 | Q9BVH7 |
| C0041296 | Tuberculosis | ACSBG2 | 81616 | acyl-CoA synthetase bubblegum family member 2 | Q5FVE4 |
| C0162309 | Adrenoleukodystrophy | ACSBG2 | 81616 | acyl-CoA synthetase bubblegum family member 2 | Q5FVE4 |
| C0021364 | Male infertility | ACSBG2 | 81616 | acyl-CoA synthetase bubblegum family member 2 | Q5FVE4 |
| C0036341 | Schizophrenia | PLA2G12A | 81579 | phospholipase A2 group XIIA | Q9BZM1 |
| C1510586 | Autism Spectrum Disorders | PLA2G12A | 81579 | phospholipase A2 group XIIA | Q9BZM1 |
| C0003850 | Arteriosclerosis | PLA2G12A | 81579 | phospholipase A2 group XIIA | Q9BZM1 |
| C0271084 | Exudative age-related macular degeneration | PLA2G12A | 81579 | phospholipase A2 group XIIA | Q9BZM1 |
| C0242383 | Age related macular degeneration | PLA2G12A | 81579 | phospholipase A2 group XIIA | Q9BZM1 |
| C0024713 | Manic Disorder | LMAN2L | 81562 | lectin, mannose binding 2 like | Q9H0V9 |
