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 42626 - 42650 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0376480 Gingival Overgrowth SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0233794 Memory impairment SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0162739 HELLP Syndrome SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C1845052 AMELOGENESIS IMPERFECTA, HYPOPLASTIC/HYPOMATURATION, X-LINKED 1 SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0085078 Lysosomal Storage Diseases SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0085409 Polyendocrinopathies, Autoimmune SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0041296 Tuberculosis SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0020538 Hypertensive disease SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0011311 Dengue Fever SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C4721555 Autoimmune hepatitis SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0004096 Asthma SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0362046 Prediabetes syndrome SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0017661 IGA Glomerulonephritis SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0038454 Cerebrovascular accident SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C3888065 ECTODERMAL DYSPLASIA 10A, HYPOHIDROTIC/HAIR/NAIL TYPE, AUTOSOMAL DOMINANT SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0042769 Virus Diseases SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0019100 Severe Dengue SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0015310 Exotropia SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0004153 Atherosclerosis SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0028738 Nystagmus SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0030312 Pancytopenia SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C1852438 CATARACT, COPPOCK-LIKE SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C3463824 MYELODYSPLASTIC SYNDROME SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0025517 Metabolic Diseases SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2
C0566602 Primary sclerosing cholangitis SLC17A5 26503 solute carrier family 17 member 5 Q9NRA2

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Last updated: August 19, 2024