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 |
---|---|---|---|---|---|
C0018801 | Heart failure | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0025202 | melanoma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0035334 | Retinitis Pigmentosa | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0344315 | Depressed mood | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0007113 | Rectal Carcinoma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0748607 | Recurrent seizure | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0020179 | Huntington Disease | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0004936 | Mental disorders | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0007102 | Malignant tumor of colon | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0038356 | Stomach Neoplasms | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0007785 | Cerebral Infarction | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1269683 | Major Depressive Disorder | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1336708 | Testicular Germ Cell Tumor | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0037822 | Speech Disorders | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1568247 | Usher Syndrome, Type I | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0011570 | Mental Depression | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
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 |
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Last updated: August 19, 2024