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 |
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