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 |
---|---|---|---|---|---|
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 |
C0027651 | Neoplasms | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C1855179 | CATARACT, ANTERIOR POLAR | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0042870 | Vitamin D Deficiency | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0023890 | Liver Cirrhosis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0012739 | Disseminated Intravascular Coagulation | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0007102 | Malignant tumor of colon | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0699790 | Colon Carcinoma | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0524851 | Neurodegenerative Disorders | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0024312 | Lymphopenia | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0023520 | Leukodystrophy | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0027059 | Myocarditis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0279000 | Liver and Intrahepatic Biliary Tract Carcinoma | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0155773 | Portal Vein Thrombosis | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
C0011847 | Diabetes | SLC17A5 | 26503 | solute carrier family 17 member 5 | Q9NRA2 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024