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.
Database | Last Updated |
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DisGeNET | February 14, 2024 |
Disease ID | Disease Name ▲ | Gene Symbol | Gene ID | Gene Name | UniProt ID |
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Cervix carcinoma
|
phosphogluconate dehydrogenase
|
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Cervix carcinoma
|
cadherin 13
|
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Cervix carcinoma
|
heparan sulfate-glucosamine 3-sulfotransferase 2
|
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Cervix carcinoma
|
TNF receptor superfamily member 10c
|
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Chagas Disease
|
eukaryotic translation initiation factor 2 subunit gamma
|
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Childhood Acute Lymphoblastic Leukemia
|
fragile histidine triad diadenosine triphosphatase
|
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Childhood Acute Lymphoblastic Leukemia
|
5-aminoimidazole-4-carboxamide ribonucleotide formyltransferase/IMP cyclohydrolase
|
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Childhood Ataxia with Central Nervous System Hypomyelinization
|
eukaryotic translation initiation factor 2 subunit gamma
|
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Childhood Hepatocellular Carcinoma
|
sulfatase 1
|
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Childhood Kidney Wilms Tumor
|
reversion inducing cysteine rich protein with kazal motifs
|
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Partly supported by NIH Common Fund Grant #1U01GM125267-01