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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Common Variable Immunodeficiency
|
heparan sulfate proteoglycan 2
|
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Dementia
|
heparan sulfate proteoglycan 2
|
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Presenile dementia
|
heparan sulfate proteoglycan 2
|
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MYELODYSPLASTIC SYNDROME
|
hemojuvelin BMP co-receptor
|
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Liver carcinoma
|
hemojuvelin BMP co-receptor
|
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Prostate carcinoma
|
hematopoietic prostaglandin D synthase
|
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Carcinoma, Transitional Cell
|
hematopoietic prostaglandin D synthase
|
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Bronchioloalveolar Adenocarcinoma
|
hematopoietic prostaglandin D synthase
|
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Adenocarcinoma
|
hematopoietic prostaglandin D synthase
|
||||
Adenocarcinoma of prostate
|
hematopoietic prostaglandin D synthase
|
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Partly supported by NIH Common Fund Grant #1U01GM125267-01