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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 |
|---|---|---|---|---|---|
| C0020224 | Polyhydramnios | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C2931001 | Congenital disorder of glycosylation type 1G | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0282577 | Congenital Disorders of Glycosylation | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0016522 | Foramen Ovale, Patent | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0035334 | Retinitis Pigmentosa | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0013604 | Edema | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0020598 | Hypocalcemia | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0035305 | Retinal Detachment | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0013274 | Patent ductus arteriosus | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C0848558 | Hypospadias | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C1837396 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ie | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C4317295 | Congenital disorder of glycosylation type 1s | ALG12 | 79087 | ALG12 alpha-1,6-mannosyltransferase | Q9BV10 |
| C1847540 | Azoospermia, Nonobstructive | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0033860 | Psoriasis | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0027651 | Neoplasms | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0011860 | Diabetes Mellitus, Non-Insulin-Dependent | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C1800706 | Idiopathic Pulmonary Fibrosis | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C1704272 | Benign Prostatic Hyperplasia | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C2239176 | Liver carcinoma | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0003850 | Arteriosclerosis | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0003872 | Arthritis, Psoriatic | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0015625 | Fanconi Anemia | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0020459 | Hyperinsulinism | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
| C0018802 | Congestive heart failure | ELOVL6 | 79071 | ELOVL fatty acid elongase 6 | Q9H5J4 |
