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 49326 - 49350 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C4552072 X-linked infantile spasms SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1449563 Cardiomyopathy, Familial Idiopathic SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0278985 Adult Extraskeletal Osteosarcoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0029408 Degenerative polyarthritis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1153706 Endometrial adenocarcinoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0279613 Childhood Alveolar Rhabdomyosarcoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0010054 Coronary Arteriosclerosis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0205822 Hibernoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0022283 Incontinentia Pigmenti Achromians SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0344315 Depressed mood SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0039103 Synovitis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0079588 Ichthyosis, X-Linked SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0239946 Fibrosis, Liver SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0029456 Osteoporosis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0699885 Carcinoma of bladder SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0032580 Adenomatous Polyposis Coli SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0003467 Anxiety SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1800706 Idiopathic Pulmonary Fibrosis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0007124 Noninfiltrating Intraductal Carcinoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0037856 Spermatic Cord Torsion SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0040213 Tietze's Syndrome SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1708716 Pericardial Solitary Fibrous Tumor SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0206717 Olfactory Neuroblastoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0041671 Attention Deficit Disorder SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0029182 orbit (eye disorders) SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7

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