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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Lysyl hydroxylase 3 deficiency
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PLOD3
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Congenital Disorders of Glycosylation (CDGs)
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DPM1-CDG
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DPM1
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Congenital Disorders of Glycosylation (CDGs)
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Fukuyama congenital muscular dystrophy
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FKTN
|
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Congenital Disorders of Glycosylation (CDGs)
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Muscular dystrophy, limb-girdle, type 2M
|
FKTN
|
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Congenital Disorders of Glycosylation (CDGs)
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Cardiomyopathy, dilated, 1X
|
FKTN
|
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Congenital Disorders of Glycosylation (CDGs)
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MPDU1-CDG
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MPDU1
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Congenital Disorders of Glycosylation (CDGs)
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Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
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B3GAT3
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Congenital Disorders of Glycosylation (CDGs)
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Spondyloepimetaphyseal dysplasia, pakistani type
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PAPSS2
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Congenital Disorders of Glycosylation (CDGs)
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Multiple congenital anomalies-hypotonia-seizures syndrome 1
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PIGN
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Congenital Disorders of Glycosylation (CDGs)
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LARGE-CDG (cong. muscular dystrophy spectrum)
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LARGE
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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