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 9951 - 9975 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C1621958 Glioblastoma Multiforme TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0006142 Malignant neoplasm of breast TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0678222 Breast Carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0020550 Hyperthyroidism TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C2239176 Liver carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0004153 Atherosclerosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0278878 Adult Glioblastoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0600139 Prostate carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0017154 Gastritis, Atrophic TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0018801 Heart failure TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0027651 Neoplasms TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0524620 Metabolic Syndrome X TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0002395 Alzheimer's Disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C1336527 Carcinoma of urinary bladder, superficial TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0020456 Hyperglycemia TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0026848 Myopathy TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0029408 Degenerative polyarthritis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0235974 Pancreatic carcinoma TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0020179 Huntington Disease TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0022658 Kidney Diseases TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0037116 Silicosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0264694 Chronic myocardial ischemia TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0235833 Congenital diaphragmatic hernia TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0020541 Portal Hypertension TM7SF2 7108 transmembrane 7 superfamily member 2 O76062
C0034069 Pulmonary Fibrosis TM7SF2 7108 transmembrane 7 superfamily member 2 O76062

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Last updated: August 19, 2024