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 49476 - 49500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▲
C0025286 Meningioma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0023895 Liver diseases SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1851585 MYELOPROLIFERATIVE DISORDER, CHRONIC, WITH EOSINOPHILIA SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0023467 Leukemia, Myelocytic, Acute SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0265004 Dilatation of aorta SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0205969 Thymic Carcinoma SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0003615 Appendicitis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0041327 Tuberculosis, Pulmonary SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0085669 Acute leukemia SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0221406 Pituitary-dependent Cushing's disease SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0280631 Leiomyosarcoma of uterus SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0279014 Childhood Germ Cell Tumor SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1561643 Chronic Kidney Diseases SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1306803 Atypical subacute thyroiditis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0020981 Angioimmunoblastic Lymphadenopathy SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0206145 Stunned Myocardium SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C1334807 Mucinous carcinoma of breast SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0206085 Kleine-Levin Syndrome SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0003857 Congenital arteriovenous malformation SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0029405 Osteitis Fibrosa Cystica SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0085413 Polycystic Kidney, Autosomal Dominant SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0007282 Carotid Stenosis SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0005956 Bone Marrow Diseases SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0278622 Adult Malignant Peripheral Nerve Sheath Tumor SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7
C0020456 Hyperglycemia SMUG1 23583 single-strand-selective monofunctional uracil-DNA glycosylase 1 Q53HV7

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Last updated: August 19, 2024