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 |
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DisGeNET | July 29, 2024 |
Disease ID | Disease Name | Gene Symbol | Gene ID | Gene Name ▲ | UniProt ID |
---|---|---|---|---|---|
C0752207 | Familial Dystonia | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0014548 | Epilepsy, Generalized | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0752206 | Dystonias, Sporadic | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C1140680 | Malignant neoplasm of ovary | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0036572 | Seizures | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0242383 | Age related macular degeneration | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0752203 | Dystonia, Primary | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0494475 | Tonic - clonic seizures | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0752202 | Childhood Onset Dystonias | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0003467 | Anxiety | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0038379 | Strabismus | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0007124 | Noninfiltrating Intraductal Carcinoma | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0010346 | Crohn Disease | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0036857 | Severe intellectual disability | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0035372 | Rett Syndrome | ALDH5A1 | 7915 | aldehyde dehydrogenase 5 family member A1 | P51649 |
C0151744 | Myocardial Ischemia | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0025958 | Microcephaly | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0086543 | Cataract | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0013421 | Dystonia | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0014544 | Epilepsy | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0220981 | Metabolic acidosis | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0279702 | Conventional (Clear Cell) Renal Cell Carcinoma | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0028754 | Obesity | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
C0026010 | Microphthalmos | ALDH6A1 | 4329 | aldehyde dehydrogenase 6 family member A1 | Q02252 |
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Last updated: August 19, 2024