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 ▼ |
---|---|---|---|---|---|
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