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
Displaying entries 6001 - 6025 of 62743 in total
Disease ID Disease Name Gene Symbol ▼ Gene ID Gene Name UniProt ID
C0004623 Bacterial Infections SLC5A1 6523 solute carrier family 5 member 1 P13866
C0021828 Intestinal Atresia SLC5A1 6523 solute carrier family 5 member 1 P13866
C0349566 Squamous cell carcinoma of tongue SLC5A1 6523 solute carrier family 5 member 1 P13866
C0032285 Pneumonia SLC5A1 6523 solute carrier family 5 member 1 P13866
C0010054 Coronary Arteriosclerosis SLC5A1 6523 solute carrier family 5 member 1 P13866
C0007131 Non-Small Cell Lung Carcinoma SLC5A1 6523 solute carrier family 5 member 1 P13866
C0023860 Listeriosis SLC5A1 6523 solute carrier family 5 member 1 P13866
C0027051 Myocardial Infarction SLC5A1 6523 solute carrier family 5 member 1 P13866
C1565489 Renal Insufficiency SLC5A1 6523 solute carrier family 5 member 1 P13866
C1449563 Cardiomyopathy, Familial Idiopathic SLC5A1 6523 solute carrier family 5 member 1 P13866
C2239176 Liver carcinoma SLC5A1 6523 solute carrier family 5 member 1 P13866
C0020428 Hyperaldosteronism SLC5A1 6523 solute carrier family 5 member 1 P13866
C0271650 Impaired glucose tolerance SLC5A1 6523 solute carrier family 5 member 1 P13866
C0007222 Cardiovascular Diseases SLC5A1 6523 solute carrier family 5 member 1 P13866
C3714636 Pneumonitis SLC5A1 6523 solute carrier family 5 member 1 P13866
C0007785 Cerebral Infarction SLC5A1 6523 solute carrier family 5 member 1 P13866
C0678222 Breast Carcinoma SLC5A1 6523 solute carrier family 5 member 1 P13866
C0338508 Optic Atrophy 1 SLC5A1 6523 solute carrier family 5 member 1 P13866
C0017658 Glomerulonephritis SLC5A1 6523 solute carrier family 5 member 1 P13866
C0007194 Hypertrophic Cardiomyopathy SLC5A1 6523 solute carrier family 5 member 1 P13866
C0023283 Leishmaniasis, Cutaneous SLC5A1 6523 solute carrier family 5 member 1 P13866
C0010691 Cystinuria SLC3A1 6519 solute carrier family 3 member 1 Q07837
C1848030 Hypotonia-Cystinuria Syndrome SLC3A1 6519 solute carrier family 3 member 1 Q07837
C0022661 Kidney Failure, Chronic SLC3A1 6519 solute carrier family 3 member 1 Q07837
C0017636 Glioblastoma SLC3A1 6519 solute carrier family 3 member 1 Q07837

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Last updated: August 19, 2024