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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 |
|---|---|---|---|---|---|
| C0001973 | Alcoholic Intoxication, Chronic | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0037369 | Smoking | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0009402 | Colorectal Carcinoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0006826 | Malignant Neoplasms | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0010068 | Coronary heart disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0024141 | Lupus Erythematosus, Systemic | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0019202 | Hepatolenticular Degeneration | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0027819 | Neuroblastoma | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C1384666 | hearing impairment | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0013595 | Eczema | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0020538 | Hypertensive disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0013336 | Dwarfism | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C1332977 | Childhood Leukemia | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C3714756 | Intellectual Disability | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C2677590 | Congenital Disorder Of Glycosylation, Type In | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C1960469 | Left ventricular noncompaction | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0028738 | Nystagmus | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C1842836 | CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Ii | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0027651 | Neoplasms | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0038379 | Strabismus | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0393593 | Dystonia Disorders | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0030567 | Parkinson Disease | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0027765 | nervous system disorder | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C0595995 | Idiopathic scoliosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
| C1858725 | NONCOMPACTION OF LEFT VENTRICULAR MYOCARDIUM, FAMILIAL ISOLATED, AUTOSOMAL DOMINANT 1 | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
