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 ▲ |
---|---|---|---|---|---|
C0079774 | Peripheral T-Cell Lymphoma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0042164 | Uveitis | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C1458155 | Mammary Neoplasms | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0001403 | Addison Disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C4551686 | Malignant neoplasm of soft tissue | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0015695 | Fatty Liver | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0024117 | Chronic Obstructive Airway Disease | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0035309 | Retinal Diseases | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0030354 | Papilloma | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C1140680 | Malignant neoplasm of ovary | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0004135 | Ataxia Telangiectasia | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0011991 | Diarrhea | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0338106 | Adenocarcinoma of colon | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C1861305 | TARSAL-CARPAL COALITION SYNDROME | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0018790 | Cardiac Arrest | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0019101 | Hemorrhagic Fever with Renal Syndrome | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0919267 | ovarian neoplasm | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0007847 | Malignant tumor of cervix | TM7SF2 | 7108 | transmembrane 7 superfamily member 2 | O76062 |
C0020490 | Hyperopia | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
C0017601 | Glaucoma | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
C0000768 | Congenital Abnormality | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
C0013336 | Dwarfism | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
C3278404 | MULTIPLE JOINT DISLOCATIONS, SHORT STATURE, AND CRANIOFACIAL DYSMORPHISM WITH OR WITHOUT CONGENITAL HEART DEFECTS | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
C0221356 | Brachycephaly | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
C0008925 | Cleft Palate | B3GAT3 | 26229 | beta-1,3-glucuronyltransferase 3 | O94766 |
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Last updated: August 19, 2024