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 39976 - 40000 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C4048328 cervical cancer GPC1 2817 glypican 1 P35052
C2239176 Liver carcinoma GPC1 2817 glypican 1 P35052
C0007137 Squamous cell carcinoma GPC1 2817 glypican 1 P35052
C1704272 Benign Prostatic Hyperplasia GPC1 2817 glypican 1 P35052
C0030297 Pancreatic Neoplasm GPC1 2817 glypican 1 P35052
C0005411 Biliary Atresia GPC1 2817 glypican 1 P35052
C0002395 Alzheimer's Disease GPC1 2817 glypican 1 P35052
C0281361 Adenocarcinoma of pancreas GPC1 2817 glypican 1 P35052
C0007102 Malignant tumor of colon GPC1 2817 glypican 1 P35052
C0020676 Hypothyroidism GPC1 2817 glypican 1 P35052
C0003873 Rheumatoid Arthritis GPC1 2817 glypican 1 P35052
C0025500 Mesothelioma GPC1 2817 glypican 1 P35052
C0001418 Adenocarcinoma GPC1 2817 glypican 1 P35052
C0302314 Xanthoma GPC1 2817 glypican 1 P35052
C0919267 ovarian neoplasm GPC1 2817 glypican 1 P35052
C0016037 Fibrodysplasia Ossificans Progressiva GPC1 2817 glypican 1 P35052
C1867773 CEREBRAL AMYLOID ANGIOPATHY, ITM2B-RELATED, 1 GPC1 2817 glypican 1 P35052
C0152013 Adenocarcinoma of lung (disorder) GPC1 2817 glypican 1 P35052
C0029089 Ophthalmoplegia GPC1 2817 glypican 1 P35052
C0010278 Craniosynostosis GPC1 2817 glypican 1 P35052
C3179455 Niemann-Pick Disease, Type C1 GPC1 2817 glypican 1 P35052
C0020635 Hypopituitarism GPC1 2817 glypican 1 P35052
C0796154 SIMPSON-GOLABI-BEHMEL SYNDROME, TYPE 1 GPC1 2817 glypican 1 P35052
C0235974 Pancreatic carcinoma GP2 2813 glycoprotein 2 P55259
C0010346 Crohn Disease GP2 2813 glycoprotein 2 P55259

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Last updated: August 19, 2024