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 58976 - 59000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0239946 Fibrosis, Liver SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0015695 Fatty Liver SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C3160718 PARKINSON DISEASE, LATE-ONSET SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
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

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024