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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 |
|---|---|---|---|---|---|
| C0023882 | Little's Disease | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0036421 | Systemic Scleroderma | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0023772 | Lipid Metabolism, Inborn Errors | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0035309 | Retinal Diseases | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C1865349 | Ethylmalonic encephalopathy | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0011854 | Diabetes Mellitus, Insulin-Dependent | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0019163 | Hepatitis B | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0025362 | Mental Retardation | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0220766 | Congenital hypoplasia of adrenal gland | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0011603 | Dermatitis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0543874 | Apraxia, oculomotor, Cogan type | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0205875 | Papillomatosis | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C0403553 | Renal dysplasia and retinal aplasia (disorder) | ALDH3A2 | 224 | aldehyde dehydrogenase 3 family member A2 | P51648 |
| C1306459 | Primary malignant neoplasm | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0740457 | Malignant neoplasm of kidney | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0002878 | Anemia, Hemolytic | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0007134 | Renal Cell Carcinoma | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0006826 | Malignant Neoplasms | ALDH9A1 | 223 | aldehyde dehydrogenase 9 family member A1 | P49189 |
| C0014544 | Epilepsy | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0235480 | Paroxysmal atrial fibrillation | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0017636 | Glioblastoma | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0278878 | Adult Glioblastoma | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C0004238 | Atrial Fibrillation | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
| C1621958 | Glioblastoma Multiforme | SLC35F1 | 222553 | solute carrier family 35 member F1 | Q5T1Q4 |
