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 |
---|---|---|---|---|---|
C0020615 | Hypoglycemia | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0018099 | Gout | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0043325 | Xanthomatosis | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C1621958 | Glioblastoma Multiforme | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0038644 | Sudden infant death syndrome | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0029456 | Osteoporosis | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C3203102 | Idiopathic pulmonary arterial hypertension | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0149745 | Oral Ulcer | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0302314 | Xanthoma | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0022658 | Kidney Diseases | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0004364 | Autoimmune Diseases | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0017636 | Glioblastoma | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0392525 | Nephrolithiasis | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C1565489 | Renal Insufficiency | SLC37A4 | 2542 | solute carrier family 37 member 4 | O43826 |
C0004153 | Atherosclerosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0011849 | Diabetes Mellitus | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0041296 | Tuberculosis | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0004238 | Atrial Fibrillation | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0011847 | Diabetes | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
C0041327 | Tuberculosis, Pulmonary | SLC39A8 | 64116 | solute carrier family 39 member 8 | Q9C0K1 |
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 |
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Last updated: August 19, 2024