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 56526 - 56550 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0400966 Non-alcoholic Fatty Liver Disease SLC2A12 154091 solute carrier family 2 member 12 Q8TD20
C0006142 Malignant neoplasm of breast SLC2A2 6514 solute carrier family 2 member 2 P11168
C3495427 Fanconi-Bickel Syndrome SLC2A2 6514 solute carrier family 2 member 2 P11168
C1257931 Mammary Neoplasms, Human SLC2A2 6514 solute carrier family 2 member 2 P11168
C0011860 Diabetes Mellitus, Non-Insulin-Dependent SLC2A2 6514 solute carrier family 2 member 2 P11168
C0007097 Carcinoma SLC2A2 6514 solute carrier family 2 member 2 P11168
C2711227 Steatohepatitis SLC2A2 6514 solute carrier family 2 member 2 P11168
C0007222 Cardiovascular Diseases SLC2A2 6514 solute carrier family 2 member 2 P11168
C0011847 Diabetes SLC2A2 6514 solute carrier family 2 member 2 P11168
C0271650 Impaired glucose tolerance SLC2A2 6514 solute carrier family 2 member 2 P11168
C2239176 Liver carcinoma SLC2A2 6514 solute carrier family 2 member 2 P11168
C0011849 Diabetes Mellitus SLC2A2 6514 solute carrier family 2 member 2 P11168
C0678222 Breast Carcinoma SLC2A2 6514 solute carrier family 2 member 2 P11168
C0400966 Non-alcoholic Fatty Liver Disease SLC2A2 6514 solute carrier family 2 member 2 P11168
C0158981 Neonatal diabetes mellitus SLC2A2 6514 solute carrier family 2 member 2 P11168
C0024523 Malabsorption Syndrome SLC2A2 6514 solute carrier family 2 member 2 P11168
C0025517 Metabolic Diseases SLC2A2 6514 solute carrier family 2 member 2 P11168
C0022658 Kidney Diseases SLC2A2 6514 solute carrier family 2 member 2 P11168
C1257958 Glucose Metabolism Disorders SLC2A2 6514 solute carrier family 2 member 2 P11168
C0015695 Fatty Liver SLC2A2 6514 solute carrier family 2 member 2 P11168
C0149782 Squamous cell carcinoma of lung SLC2A2 6514 solute carrier family 2 member 2 P11168
C0017919 Glycogen Storage Disease SLC2A2 6514 solute carrier family 2 member 2 P11168
C3536983 Familial Hypophosphatemic Rickets SLC2A2 6514 solute carrier family 2 member 2 P11168
C0949541 Hurthle Cell Tumor SLC2A2 6514 solute carrier family 2 member 2 P11168
C0011334 Dental caries SLC2A2 6514 solute carrier family 2 member 2 P11168

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Last updated: August 19, 2024