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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 |
|---|---|---|---|---|---|
| C0678222 | Breast Carcinoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0010346 | Crohn Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0029408 | Degenerative polyarthritis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0236970 | Alcohol-Induced Disorders | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0039585 | Androgen-Insensitivity Syndrome | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0700095 | Central neuroblastoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0020179 | Huntington Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C4225234 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE IIn | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0243026 | Sepsis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0684276 | Hypsarrhythmia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0020490 | Hyperopia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C1263846 | Attention deficit hyperactivity disorder | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0018802 | Congestive heart failure | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0036341 | Schizophrenia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0018801 | Heart failure | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0004106 | Astigmatism | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0282577 | Congenital Disorders of Glycosylation | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0162429 | Malnutrition | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C1531647 | Cerebral ventriculomegaly | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0038454 | Cerebrovascular accident | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0013421 | Dystonia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0742343 | Acute Chest Syndrome | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0002871 | Anemia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0236664 | Alcohol-Related Disorders | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0751651 | Mitochondrial Diseases | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
