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 41576 - 41600 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID Gene Name ▲ UniProt ID
C3888317 Sialidosis, type 2 NEU1 4758 neuraminidase 1 Q99519
C0033687 Proteinuria NEU1 4758 neuraminidase 1 Q99519
C1332166 Adenocarcinoma of the gastroesophageal junction NEU1 4758 neuraminidase 1 Q99519
C0035309 Retinal Diseases NEU1 4758 neuraminidase 1 Q99519
C0018784 Sensorineural Hearing Loss (disorder) NEU1 4758 neuraminidase 1 Q99519
C0206701 Cystadenocarcinoma, Serous NEU1 4758 neuraminidase 1 Q99519
C2607914 Allergic rhinitis (disorder) NEU1 4758 neuraminidase 1 Q99519
C0007138 Carcinoma, Transitional Cell NEU1 4758 neuraminidase 1 Q99519
C2239176 Liver carcinoma NEU1 4758 neuraminidase 1 Q99519
C2718068 beta-Galactosidase Deficiency NEU1 4758 neuraminidase 1 Q99519
C0028738 Nystagmus NEU1 4758 neuraminidase 1 Q99519
C0009324 Ulcerative Colitis NEU1 4758 neuraminidase 1 Q99519
C0751780 Biotin-Responsive Encephalopathy NEU1 4758 neuraminidase 1 Q99519
C0684249 Carcinoma of lung NEU1 4758 neuraminidase 1 Q99519
C0870082 Hyperkeratosis NEU1 4758 neuraminidase 1 Q99519
C0036341 Schizophrenia NEU1 4758 neuraminidase 1 Q99519
C0278878 Adult Glioblastoma NEU1 4758 neuraminidase 1 Q99519
C0025289 Meningitis NEU1 4758 neuraminidase 1 Q99519
C0019270 Hernia NEU1 4758 neuraminidase 1 Q99519
C0025202 melanoma NEU1 4758 neuraminidase 1 Q99519
C0750952 Biliary Tract Cancer NEU1 4758 neuraminidase 1 Q99519
C0013336 Dwarfism NEU1 4758 neuraminidase 1 Q99519
C0035412 Rhabdomyosarcoma NEU2 4759 neuraminidase 2 Q9Y3R4
C0699791 Stomach Carcinoma NEU2 4759 neuraminidase 2 Q9Y3R4
C0600139 Prostate carcinoma NEU2 4759 neuraminidase 2 Q9Y3R4

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Last updated: August 19, 2024