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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 |
|---|---|---|---|---|---|
| C0020676 | Hypothyroidism | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0023891 | Liver Cirrhosis, Alcoholic | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0041296 | Tuberculosis | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0346647 | Malignant neoplasm of pancreas | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0024620 | Primary Malignant Liver Neoplasm | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0041234 | Chagas Disease | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0034150 | Purpura | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0162309 | Adrenoleukodystrophy | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0007785 | Cerebral Infarction | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0920350 | Autoimmune thyroiditis | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C1868679 | GRISCELLI SYNDROME, TYPE 2 | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0525045 | Mood Disorders | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0029463 | Osteosarcoma | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0011884 | Diabetic Retinopathy | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0751753 | Carbamoyl-Phosphate Synthase I Deficiency Disease | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0027092 | Myopia | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0279070 | Adult Oligodendroglioma | GLUL | 2752 | glutamate-ammonia ligase | P15104 |
| C0751748 | Nonketotic Hyperglycinemia | AMT | 275 | aminomethyltransferase | P48728 |
| C0036572 | Seizures | AMT | 275 | aminomethyltransferase | P48728 |
| C0010043 | Corneal Ulcer | AMT | 275 | aminomethyltransferase | P48728 |
| C0030305 | Pancreatitis | AMT | 275 | aminomethyltransferase | P48728 |
| C0027066 | Myoclonus | AMT | 275 | aminomethyltransferase | P48728 |
| C0795830 | CHROMOSOME 9p DELETION SYNDROME | AMT | 275 | aminomethyltransferase | P48728 |
| C0001122 | Acidosis | AMT | 275 | aminomethyltransferase | P48728 |
| C0011570 | Mental Depression | AMT | 275 | aminomethyltransferase | P48728 |
