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 9651 - 9675 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0014544 Epilepsy SLC35A2 7355 solute carrier family 35 member A2 P78381
C0039685 Tetralogy of Fallot SLC35A2 7355 solute carrier family 35 member A2 P78381
C0007097 Carcinoma SLC35A2 7355 solute carrier family 35 member A2 P78381
C0020433 Hyperbilirubinemia SLC35A2 7355 solute carrier family 35 member A2 P78381
C0677886 Epithelial ovarian cancer SLC35A2 7355 solute carrier family 35 member A2 P78381
C0520680 Sleep Apnea, Central SLC35A2 7355 solute carrier family 35 member A2 P78381
C3714756 Intellectual Disability SLC35A2 7355 solute carrier family 35 member A2 P78381
C1306459 Primary malignant neoplasm SLC35A2 7355 solute carrier family 35 member A2 P78381
C0279628 Adenocarcinoma Of Esophagus SLC35A2 7355 solute carrier family 35 member A2 P78381
C0678222 Breast Carcinoma SLC35A2 7355 solute carrier family 35 member A2 P78381
C0085584 Encephalopathies SLC35A2 7355 solute carrier family 35 member A2 P78381
C0002878 Anemia, Hemolytic SLC35A2 7355 solute carrier family 35 member A2 P78381
C0036439 Scoliosis, unspecified SLC35A2 7355 solute carrier family 35 member A2 P78381
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

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Last updated: August 19, 2024