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 8726 - 8750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C0011880 Diabetic Ketoacidosis UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C0024117 Chronic Obstructive Airway Disease UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C4048328 cervical cancer UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C0020456 Hyperglycemia UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C0011581 Depressive disorder UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C0677886 Epithelial ovarian cancer UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C0025312 Meningomyelocele UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C0018790 Cardiac Arrest UGCG 7357 UDP-glucose ceramide glucosyltransferase Q16739
C0006826 Malignant Neoplasms UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0019196 Hepatitis C UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0600139 Prostate carcinoma UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0947622 Cholecystolithiasis UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0221757 alpha 1-Antitrypsin Deficiency UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0036572 Seizures UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0017551 Gilbert Disease (disorder) UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0002895 Anemia, Sickle Cell UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0271979 Thalassemia Intermedia UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0008350 Cholelithiasis UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0023895 Liver diseases UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0857007 Hyperbilirubinemia, Neonatal UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0010324 Crigler Najjar syndrome, type 1 UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0020433 Hyperbilirubinemia UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0027947 Neutropenia UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0023530 Leukopenia UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2
C0011226 Hepatitis D Infection UGGT1 56886 UDP-glucose glycoprotein glucosyltransferase 1 Q9NYU2

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