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 58426 - 58450 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name UniProt ID ▼
C0027819 Neuroblastoma B4GALT3 8703 beta-1,4-galactosyltransferase 3 O60512
C0699885 Carcinoma of bladder B4GALT3 8703 beta-1,4-galactosyltransferase 3 O60512
C0684249 Carcinoma of lung TPST1 8460 tyrosylprotein sulfotransferase 1 O60507
C0009402 Colorectal Carcinoma TPST1 8460 tyrosylprotein sulfotransferase 1 O60507
C0242379 Malignant neoplasm of lung TPST1 8460 tyrosylprotein sulfotransferase 1 O60507
C0003868 Arthritis, Gouty TPST1 8460 tyrosylprotein sulfotransferase 1 O60507
C0027651 Neoplasms TPST1 8460 tyrosylprotein sulfotransferase 1 O60507
C0028064 Niemann-Pick Diseases OGA 10724 O-GlcNAcase O60502
C0030567 Parkinson Disease OGA 10724 O-GlcNAcase O60502
C0039373 Tay-Sachs Disease OGA 10724 O-GlcNAcase O60502
C0011847 Diabetes OGA 10724 O-GlcNAcase O60502
C0087012 Ataxia, Spinocerebellar OGA 10724 O-GlcNAcase O60502
C0011849 Diabetes Mellitus OGA 10724 O-GlcNAcase O60502
C0036161 Sandhoff Disease OGA 10724 O-GlcNAcase O60502
C1565489 Renal Insufficiency OGA 10724 O-GlcNAcase O60502
C0040963 Tricuspid Valve Stenosis OGA 10724 O-GlcNAcase O60502
C0524851 Neurodegenerative Disorders OGA 10724 O-GlcNAcase O60502
C0002395 Alzheimer's Disease OGA 10724 O-GlcNAcase O60502
C0268274 Gangliosidoses, GM2 OGA 10724 O-GlcNAcase O60502
C0020295 Hydronephrosis OGA 10724 O-GlcNAcase O60502
C0242422 Parkinsonian Disorders OGA 10724 O-GlcNAcase O60502
C0021831 Intestinal Diseases OGA 10724 O-GlcNAcase O60502
C0022658 Kidney Diseases OGA 10724 O-GlcNAcase O60502
C0086445 Idiopathic Membranous Glomerulonephritis OGA 10724 O-GlcNAcase O60502
C0085078 Lysosomal Storage Diseases OGA 10724 O-GlcNAcase O60502

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Last updated: August 19, 2024