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 ▼ |
---|---|---|---|---|---|
C0002871 | Anemia | PCCA | 5095 | propionyl-CoA carboxylase subunit alpha | P05165 |
C0027051 | Myocardial Infarction | LGALS2 | 3957 | galectin 2 | P05162 |
C0015934 | Fetal Growth Retardation | LGALS2 | 3957 | galectin 2 | P05162 |
C0021390 | Inflammatory Bowel Diseases | LGALS2 | 3957 | galectin 2 | P05162 |
C0024623 | Malignant neoplasm of stomach | LGALS2 | 3957 | galectin 2 | P05162 |
C0011849 | Diabetes Mellitus | LGALS2 | 3957 | galectin 2 | P05162 |
C0007222 | Cardiovascular Diseases | LGALS2 | 3957 | galectin 2 | P05162 |
C0392662 | Angiostrongyliasis | LGALS2 | 3957 | galectin 2 | P05162 |
C0003873 | Rheumatoid Arthritis | LGALS2 | 3957 | galectin 2 | P05162 |
C0524620 | Metabolic Syndrome X | LGALS2 | 3957 | galectin 2 | P05162 |
C1956346 | Coronary Artery Disease | LGALS2 | 3957 | galectin 2 | P05162 |
C0020538 | Hypertensive disease | LGALS2 | 3957 | galectin 2 | P05162 |
C0010054 | Coronary Arteriosclerosis | LGALS2 | 3957 | galectin 2 | P05162 |
C0002736 | Amyotrophic Lateral Sclerosis | LGALS2 | 3957 | galectin 2 | P05162 |
C0016085 | Filariasis | LGALS2 | 3957 | galectin 2 | P05162 |
C0038454 | Cerebrovascular accident | LGALS2 | 3957 | galectin 2 | P05162 |
C0027651 | Neoplasms | LGALS2 | 3957 | galectin 2 | P05162 |
C0009319 | Colitis | LGALS2 | 3957 | galectin 2 | P05162 |
C0520459 | Necrotizing Enterocolitis | LGALS2 | 3957 | galectin 2 | P05162 |
C0948008 | Ischemic stroke | LGALS2 | 3957 | galectin 2 | P05162 |
C0024534 | Malaria, Cerebral | LGALS2 | 3957 | galectin 2 | P05162 |
C3151055 | ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0848558 | Hypospadias | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C1704272 | Benign Prostatic Hyperplasia | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
C0023903 | Liver neoplasms | CYP11A1 | 1583 | cytochrome P450 family 11 subfamily A member 1 | P05108 |
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Last updated: August 19, 2024