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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Autosomal recessive multiple epiphyseal dysplasia
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SLC26A2
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Congenital Disorders of Glycosylation (CDGs)
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SLC35D1-CDG
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SLC35D1
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Congenital Disorders of Glycosylation (CDGs)
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Tn polyagglutination syndrome, somatic (SOMATIC MUTATION)
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C1GALT1C1
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Congenital Disorders of Glycosylation (CDGs)
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GALNT3-CDG
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GALNT3
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Congenital Disorders of Glycosylation (CDGs)
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B3GALTL-CDG
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B3GALTL
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Congenital Disorders of Glycosylation (CDGs)
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LFNG-CDG
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LFNG
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Congenital Disorders of Glycosylation (CDGs)
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Ehlers-Danlos syndrome, type VI
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PLOD1
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Congenital Disorders of Glycosylation (CDGs)
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Bruck syndrome 2
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PLOD2
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Congenital Disorders of Glycosylation (CDGs)
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Lysyl hydroxylase 3 deficiency
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PLOD3
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Congenital Disorders of Glycosylation (CDGs)
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ST3GAL5-CDG
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SIAT9
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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