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 60626 - 60650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0017574 Gingivitis OGA 10724 O-GlcNAcase O60502
C0678222 Breast Carcinoma OGA 10724 O-GlcNAcase O60502
C1140680 Malignant neoplasm of ovary OGA 10724 O-GlcNAcase O60502
C0349653 Congenital disorder of glycosylation type 1A OGA 10724 O-GlcNAcase O60502
C0011860 Diabetes Mellitus, Non-Insulin-Dependent OGA 10724 O-GlcNAcase O60502
C0009402 Colorectal Carcinoma OGA 10724 O-GlcNAcase O60502
C0003507 Aortic Valve Stenosis OGA 10724 O-GlcNAcase O60502
C0085084 Motor Neuron Disease OGA 10724 O-GlcNAcase O60502
C1561643 Chronic Kidney Diseases OGA 10724 O-GlcNAcase O60502
C0003850 Arteriosclerosis OGA 10724 O-GlcNAcase O60502
C0020538 Hypertensive disease OGA 10724 O-GlcNAcase O60502
C0013595 Eczema OGA 10724 O-GlcNAcase O60502
C0268596 Multiple Acyl Coenzyme A Dehydrogenase Deficiency OGA 10724 O-GlcNAcase O60502
C0006142 Malignant neoplasm of breast OGA 10724 O-GlcNAcase O60502
C2749283 Gm2-Gangliosidosis, Variant B1 OGA 10724 O-GlcNAcase O60502
C1306459 Primary malignant neoplasm OGA 10724 O-GlcNAcase O60502
C0013384 Dyskinetic syndrome OGA 10724 O-GlcNAcase O60502
C0086647 Mucopolysaccharidosis Type IIIA OGA 10724 O-GlcNAcase O60502
C1848922 Hexosaminidase alpha-Subunit Deficiency (Variant B) OGA 10724 O-GlcNAcase O60502
C0036572 Seizures OGA 10724 O-GlcNAcase O60502
C0030319 Panic Disorder OGA 10724 O-GlcNAcase O60502
C4721610 Carcinoma, Ovarian Epithelial OGA 10724 O-GlcNAcase O60502
C2239176 Liver carcinoma OGA 10724 O-GlcNAcase O60502
C1704321 Nephrotic Syndrome, Minimal Change OGA 10724 O-GlcNAcase O60502
C0949664 Tauopathies OGA 10724 O-GlcNAcase O60502

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Last updated: August 19, 2024