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 10476 - 10500 of 62743 in total
Disease ID Disease Name Gene Symbol Gene ID ▼ Gene Name UniProt ID
C0079154 Congenital Nonbullous Ichthyosiform Erythroderma SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0041834 Erythema SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0020678 Hypotrichosis SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C1565489 Renal Insufficiency SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0243026 Sepsis SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0020758 Congenital ichthyosis SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0020757 Ichthyoses SULT2B1 6820 sulfotransferase family 2B member 1 O00204
C0009398 Color vision defect ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0020757 Ichthyoses ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0242383 Age related macular degeneration ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0036572 Seizures ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0456909 Blindness ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0020620 Hypohidrosis ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0265961 Erythrokeratodermia variabilis ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C2239176 Liver carcinoma ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C1838644 Stargardt disease 3 ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0015397 Disorder of eye ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C4282180 Juvenile macular degeneration ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C1855465 STARGARDT DISEASE 1 (disorder) ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C1858080 Retinal Dystrophy, Early Onset Severe ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0028738 Nystagmus ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C1851481 Erythrokeratodermia with ataxia ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0024437 Macular degeneration ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C0524851 Neurodegenerative Disorders ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5
C3489532 Cone-Rod Dystrophy 2 ELOVL4 6785 ELOVL fatty acid elongase 4 Q9GZR5

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Last updated: August 19, 2024