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 3126 - 3150 of 62743 in total
Disease ID Disease Name Gene Symbol ▲ Gene ID Gene Name UniProt ID
C2239176 Liver carcinoma AGPS 8540 alkylglycerone phosphate synthase O00116
C0162824 Dermatitis, Photoallergic AGPS 8540 alkylglycerone phosphate synthase O00116
C0017638 Glioma AGPS 8540 alkylglycerone phosphate synthase O00116
C0549473 Thyroid carcinoma AGPS 8540 alkylglycerone phosphate synthase O00116
C0040136 Thyroid Neoplasm AGPS 8540 alkylglycerone phosphate synthase O00116
C3808739 MYASTHENIC SYNDROME, CONGENITAL, 8 AGRN 375790 agrin O00468
C0023467 Leukemia, Myelocytic, Acute AGRN 375790 agrin O00468
C0152013 Adenocarcinoma of lung (disorder) AGRN 375790 agrin O00468
C0028738 Nystagmus AGRN 375790 agrin O00468
C0238463 Papillary thyroid carcinoma AGRN 375790 agrin O00468
C0036572 Seizures AGRN 375790 agrin O00468
C0018784 Sensorineural Hearing Loss (disorder) AGRN 375790 agrin O00468
C0751883 Congenital Myasthenic Syndromes, Postsynaptic AGRN 375790 agrin O00468
C0751882 Myasthenic Syndromes, Congenital AGRN 375790 agrin O00468
C0002395 Alzheimer's Disease AGRN 375790 agrin O00468
C0026998 Acute Myeloid Leukemia, M1 AGRN 375790 agrin O00468
C0014877 Esotropia AGRN 375790 agrin O00468
C1306459 Primary malignant neoplasm AGRN 375790 agrin O00468
C0520680 Sleep Apnea, Central AGRN 375790 agrin O00468
C0017168 Gastroesophageal reflux disease AGRN 375790 agrin O00468
C1276035 Pena-Shokeir syndrome type I AGRN 375790 agrin O00468
C0751885 Myasthenic Syndromes, Congenital, Slow Channel AGRN 375790 agrin O00468
C0751884 Congenital Myasthenic Syndromes, Presynaptic AGRN 375790 agrin O00468
C4082299 Bulbar palsy AGRN 375790 agrin O00468
C0029089 Ophthalmoplegia AGRN 375790 agrin O00468

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Last updated: August 19, 2024