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 ▲ |
---|---|---|---|---|---|
C0017661 | IGA Glomerulonephritis | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0376358 | Malignant neoplasm of prostate | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0039101 | synovial sarcoma | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1850889 | MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2B | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0020615 | Hypoglycemia | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0686353 | Muscular Dystrophies, Limb-Girdle | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0041349 | Nephritis, Tubulointerstitial | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C4551858 | Vesicoureteral Reflux 1 | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0020505 | Hyperphagia | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0005745 | Blepharoptosis | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0085580 | Essential Hypertension | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1857389 | Cystinuria, Type B | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C1565489 | Renal Insufficiency | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0024796 | Marfan Syndrome | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0020538 | Hypertensive disease | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0030319 | Panic Disorder | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0011849 | Diabetes Mellitus | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0001125 | Acidosis, Lactic | SLC3A1 | 6519 | solute carrier family 3 member 1 | Q07837 |
C0004943 | Behcet Syndrome | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0020437 | Hypercalcemia | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0751967 | Multiple Sclerosis, Relapsing-Remitting | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0006142 | Malignant neoplasm of breast | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C1337013 | Differentiated Thyroid Gland Carcinoma | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0151468 | Thyroid Gland Follicular Adenoma | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
C0007114 | Malignant neoplasm of skin | CYP24A1 | 1591 | cytochrome P450 family 24 subfamily A member 1 | Q07973 |
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Last updated: August 19, 2024