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 |
---|---|---|---|---|---|
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0345904 | Malignant neoplasm of liver | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0007131 | Non-Small Cell Lung Carcinoma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0007137 | Squamous cell carcinoma | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1449563 | Cardiomyopathy, Familial Idiopathic | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0002395 | Alzheimer's Disease | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0009691 | Congenital cataract | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0085096 | Peripheral Vascular Diseases | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0021775 | Intermittent Claudication | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C1832661 | ANOPHTHALMIA AND PULMONARY HYPOPLASIA | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C2931205 | Usher syndrome, type 1A | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
C0007222 | Cardiovascular Diseases | ALDH7A1 | 501 | aldehyde dehydrogenase 7 family member A1 | P49419 |
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 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024