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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 ▲ |
|---|---|---|---|---|---|
| C0006826 | Malignant Neoplasms | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
| C0268576 | Hyperleucinemia | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
| C0595989 | Carcinoma of larynx | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
| C1969443 | Trifunctional Protein Deficiency With Myopathy And Neuropathy | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
| C0015695 | Fatty Liver | HADH | 3033 | hydroxyacyl-CoA dehydrogenase | Q16836 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | ST3GAL2 | 6483 | ST3 beta-galactoside alpha-2,3-sialyltransferase 2 | Q16842 |
| C0086651 | Mucopolysaccharidosis, MPS-IV-A | ST3GAL2 | 6483 | ST3 beta-galactoside alpha-2,3-sialyltransferase 2 | Q16842 |
| C3160718 | PARKINSON DISEASE, LATE-ONSET | ST3GAL2 | 6483 | ST3 beta-galactoside alpha-2,3-sialyltransferase 2 | Q16842 |
| C0007134 | Renal Cell Carcinoma | ST3GAL2 | 6483 | ST3 beta-galactoside alpha-2,3-sialyltransferase 2 | Q16842 |
| C0026946 | Mycoses | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0041234 | Chagas Disease | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0085436 | Meningitis, Cryptococcal | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0006826 | Malignant Neoplasms | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0009186 | Coccidioidomycosis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0041296 | Tuberculosis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0023895 | Liver diseases | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0023281 | Leishmaniasis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0006840 | Candidiasis | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0032460 | Polycystic Ovary Syndrome | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0220724 | CONSTRICTING BANDS, CONGENITAL | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C1306459 | Primary malignant neoplasm | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0010414 | Infection by Cryptococcus neoformans | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0346647 | Malignant neoplasm of pancreas | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0022283 | Incontinentia Pigmenti Achromians | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
| C0235974 | Pancreatic carcinoma | CYP51A1 | 1595 | cytochrome P450 family 51 subfamily A member 1 | Q16850 |
