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 61476 - 61500 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C0023473 Myeloid Leukemia, Chronic UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0020433 Hyperbilirubinemia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0376358 Malignant neoplasm of prostate UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0018790 Cardiac Arrest UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0039730 Thalassemia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0027651 Neoplasms UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0699885 Carcinoma of bladder UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0005283 beta Thalassemia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0011991 Diarrhea UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0947622 Cholecystolithiasis UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0011860 Diabetes Mellitus, Non-Insulin-Dependent UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0546837 Malignant neoplasm of esophagus UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0002895 Anemia, Sickle Cell UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0010414 Infection by Cryptococcus neoformans UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0007097 Carcinoma UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0152018 Esophageal carcinoma UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0006142 Malignant neoplasm of breast UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0017205 Gaucher Disease UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0023530 Leukopenia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0279626 Squamous cell carcinoma of esophagus UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0400966 Non-alcoholic Fatty Liver Disease UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0027947 Neutropenia UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0017921 Glycogen storage disease type II UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C2931132 Crigler Najjar syndrome, type 2 UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9
C0699889 Malignant Female Reproductive System Neoplasm UGT1A8 54576 UDP glucuronosyltransferase family 1 member A8 Q9HAW9

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