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 |
---|---|---|---|---|---|
C0010278 | Craniosynostosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0021390 | Inflammatory Bowel Diseases | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0023418 | leukemia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0036572 | Seizures | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0003850 | Arteriosclerosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0023264 | Leigh Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0006142 | Malignant neoplasm of breast | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0013222 | Drug Use Disorders | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0033847 | Pseudoxanthoma Elasticum | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0011854 | Diabetes Mellitus, Insulin-Dependent | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C1867450 | Pseudoxanthoma Elasticum, Incomplete | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0018802 | Congestive heart failure | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0022658 | Kidney Diseases | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0002982 | Angioid Streaks | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C4014294 | DESBUQUOIS DYSPLASIA 2 | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0008925 | Cleft Palate | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0432242 | Desbuquois syndrome | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0158266 | Intervertebral Disc Degeneration | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0702166 | Acne | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0021775 | Intermittent Claudication | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0038586 | Substance Use Disorders | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0036439 | Scoliosis, unspecified | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0018818 | Ventricular Septal Defects | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0038580 | Substance Dependence | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
C0015934 | Fetal Growth Retardation | XYLT1 | 64131 | xylosyltransferase 1 | Q86Y38 |
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Last updated: August 19, 2024