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 |
|---|---|---|---|---|---|
| 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 |
| C0036341 | Schizophrenia | ALDH3B1 | 221 | aldehyde dehydrogenase 3 family member B1 | P43353 |
| C0036349 | Paranoid Schizophrenia | ALDH3B1 | 221 | aldehyde dehydrogenase 3 family member B1 | P43353 |
| C0007134 | Renal Cell Carcinoma | ALDH3B1 | 221 | aldehyde dehydrogenase 3 family member B1 | P43353 |
| C0001973 | Alcoholic Intoxication, Chronic | ALDH3B2 | 222 | aldehyde dehydrogenase 3 family member B2 | P48448 |
| C0268631 | succinic semialdehyde dehydrogenase deficiency | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0270853 | Juvenile Myoclonic Epilepsy | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0014544 | Epilepsy | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0026650 | Movement Disorders | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0752205 | Dystonia, Secondary | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0393593 | Dystonia Disorders | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0038220 | Status Epilepticus | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
| C0520947 | Clumsiness - motor delay | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
