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 53051 - 53075 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▲ Gene Name UniProt ID
C0005684 Malignant neoplasm of urinary bladder SLC35A2 7355 solute carrier family 35 member A2 P78381
C0020490 Hyperopia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0684276 Hypsarrhythmia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0282577 Congenital Disorders of Glycosylation SLC35A2 7355 solute carrier family 35 member A2 P78381
C0020615 Hypoglycemia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0947622 Cholecystolithiasis SLC35A2 7355 solute carrier family 35 member A2 P78381
C1332979 Childhood Lymphoma SLC35A2 7355 solute carrier family 35 member A2 P78381
C0025958 Microcephaly SLC35A2 7355 solute carrier family 35 member A2 P78381
C0037769 West Syndrome SLC35A2 7355 solute carrier family 35 member A2 P78381
C0024299 Lymphoma SLC35A2 7355 solute carrier family 35 member A2 P78381
C0546837 Malignant neoplasm of esophagus SLC35A2 7355 solute carrier family 35 member A2 P78381
C0023895 Liver diseases SLC35A2 7355 solute carrier family 35 member A2 P78381
C1636149 Macular dystrophy, corneal type 1 SLC35A2 7355 solute carrier family 35 member A2 P78381
C0002395 Alzheimer's Disease SLC35A2 7355 solute carrier family 35 member A2 P78381
C0002875 Cooley's anemia SLC35A2 7355 solute carrier family 35 member A2 P78381
C1527366 Salaam Seizures SLC35A2 7355 solute carrier family 35 member A2 P78381
C0014859 Esophageal Neoplasms SLC35A2 7355 solute carrier family 35 member A2 P78381
C0221023 Cyclic neutropenia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0152018 Esophageal carcinoma SLC35A2 7355 solute carrier family 35 member A2 P78381
C0013336 Dwarfism SLC35A2 7355 solute carrier family 35 member A2 P78381
C0003081 Anisometropia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0524620 Metabolic Syndrome X SLC35A2 7355 solute carrier family 35 member A2 P78381
C0400966 Non-alcoholic Fatty Liver Disease SLC35A2 7355 solute carrier family 35 member A2 P78381
C0857007 Hyperbilirubinemia, Neonatal SLC35A2 7355 solute carrier family 35 member A2 P78381
C4721610 Carcinoma, Ovarian Epithelial SLC35A2 7355 solute carrier family 35 member A2 P78381

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Last updated: August 19, 2024