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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 |
|---|---|---|---|---|---|
| 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 |
| C0020538 | Hypertensive disease | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0235527 | Heart Failure, Right-Sided | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C2239176 | Liver carcinoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C4551472 | Hypertrophic obstructive cardiomyopathy | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C2939447 | Right ventricular failure | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0009691 | Congenital cataract | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0011849 | Diabetes Mellitus | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0524620 | Metabolic Syndrome X | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C2675528 | Spastic Paraplegia 42, Autosomal Dominant | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0001418 | Adenocarcinoma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0004096 | Asthma | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
| C0003850 | Arteriosclerosis | SLC33A1 | 9197 | solute carrier family 33 member 1 | O00400 |
