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 3676 - 3700 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0023290 Leishmaniasis, Visceral SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0023895 Liver diseases SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0011860 Diabetes Mellitus, Non-Insulin-Dependent SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0009443 Common Cold SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0011570 Mental Depression SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0029408 Degenerative polyarthritis SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0019196 Hepatitis C SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0520679 Sleep Apnea, Obstructive SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C1096902 Infantile Sialic Acid Storage Disease SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0018801 Heart failure SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0020473 Hyperlipidemia SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0231528 Myalgia SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0011991 Diarrhea SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0003850 Arteriosclerosis SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0023092 Lassa Fever SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0025202 melanoma SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0024535 Malaria, Falciparum SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0022661 Kidney Failure, Chronic SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0022658 Kidney Diseases SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C1848201 Subcortical Band Heterotopia SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0342751 Generalized glycogen storage disease of infants SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0235946 Cerebral atrophy SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0015696 Fatty Liver, Alcoholic SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0524620 Metabolic Syndrome X SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0155877 Allergic asthma SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2

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Last updated: August 19, 2024