GDGDB is a database of glycan-related diseases and their responsible genes.
Database | Last Updated |
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Glyco-Disease Genes Database (GDGDB) | January 25, 2017 |
Concept UI | Disease Name | Gene Symbol | Disease Name Aliases | Disease Type | UniProt ID | Disease IDs ▼ |
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Paroxysmal nocturnal hemoglobinuria, somatic (SOMATIC MUTATION)
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PIGA
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Congenital Disorders of Glycosylation (CDGs)
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PIGM-CDG
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PIGM
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Congenital Disorders of Glycosylation (CDGs)
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PMM2-CDG, infantile multisystem stage
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PMM2
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Congenital Disorders of Glycosylation (CDGs)
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PMM2-CDG, late-infantile and childhood ataxia-intellectual disability stage
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PMM2
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Congenital Disorders of Glycosylation (CDGs)
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PMM2-CDG, adult stable disability stage
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PMM2
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Congenital Disorders of Glycosylation (CDGs)
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DPM3-CDG
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DPM3
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Congenital Disorders of Glycosylation (CDGs)
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ALG11-CDG
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ALG11
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Congenital Disorders of Glycosylation (CDGs)
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SRD5A3-CDG
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SRD5A3
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Congenital Disorders of Glycosylation (CDGs)
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DDOST-CDG
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DDOST
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Congenital Disorders of Glycosylation (CDGs)
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ALG13-CDG
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ALG13
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Congenital Disorders of Glycosylation (CDGs)
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01