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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 |
|---|---|---|---|---|---|
| C0041948 | Uremia | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0600139 | Prostate carcinoma | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0023890 | Liver Cirrhosis | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0376358 | Malignant neoplasm of prostate | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0027651 | Neoplasms | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0678222 | Breast Carcinoma | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0345904 | Malignant neoplasm of liver | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0524851 | Neurodegenerative Disorders | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0002395 | Alzheimer's Disease | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0009806 | Constipation | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0205823 | Pleomorphic Lipoma | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C1837218 | Cleft palate, isolated | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0020619 | Hypogonadism | ATRNL1 | 26033 | attractin like 1 | Q5VV63 |
| C0007131 | Non-Small Cell Lung Carcinoma | B3GALNT1 | 8706 | beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) | O75752 |
| C0027651 | Neoplasms | B3GALNT1 | 8706 | beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) | O75752 |
| C1335302 | Pancreatic Ductal Adenocarcinoma | B3GALNT1 | 8706 | beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) | O75752 |
| C0006118 | Brain Neoplasms | B3GALNT1 | 8706 | beta-1,3-N-acetylgalactosaminyltransferase 1 (globoside blood group) | O75752 |
| C3665347 | Visual Impairment | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C0027092 | Myopia | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C0026850 | Muscular Dystrophy | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C0018784 | Sensorineural Hearing Loss (disorder) | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C0854723 | Retinal Dystrophies | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C0241005 | Creatine phosphokinase serum increased | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C3554638 | MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYE ANOMALIES), TYPE A, 11 | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
| C0086543 | Cataract | B3GALNT2 | 148789 | beta-1,3-N-acetylgalactosaminyltransferase 2 | Q8NCR0 |
