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 52726 - 52750 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0151744 Myocardial Ischemia TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1510586 Autism Spectrum Disorders TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0302592 Cervix carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0008479 Chondrosarcoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0003864 Arthritis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0812413 Malignant Pleural Mesothelioma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0162871 Aortic Aneurysm, Abdominal TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1861172 Venous Thromboembolism TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0014522 Epidermodysplasia Verruciformis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0400966 Non-alcoholic Fatty Liver Disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0010068 Coronary heart disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0281361 Adenocarcinoma of pancreas TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1261473 Sarcoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0033575 Prostatic Diseases TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0029172 Oral Submucous Fibrosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0279702 Conventional (Clear Cell) Renal Cell Carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0014859 Esophageal Neoplasms TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0265950 Venous malformation TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C2711227 Steatohepatitis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0017636 Glioblastoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0030567 Parkinson Disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0019829 Hodgkin Disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1449563 Cardiomyopathy, Familial Idiopathic TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0242379 Malignant neoplasm of lung TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0346153 Breast Cancer, Familial TM7SF2 7108 transmembrane 7 superfamily member 2 O76062

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Last updated: August 19, 2024