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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PGM1-CDG
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PGM1
|
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Congenital Disorders of Glycosylation (CDGs)
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TMEM165-CDG
|
TMEM165
|
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Congenital Disorders of Glycosylation (CDGs)
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COG6-CDG
|
COG6
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Myasthenia, congenital, with tubular aggregates 1
|
GFPT1
|
|
Congenital Disorders of Glycosylation (CDGs)
|
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Mental retardation, autosomal recessive 15
|
MAN1B1
|
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Congenital Disorders of Glycosylation (CDGs)
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Mental retardation, autosomal recessive 12
|
ST3GAL3
|
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Congenital Disorders of Glycosylation (CDGs)
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Multiple joint dislocations, short stature, craniofacial dysmorphism, and congenital heart defects
|
B3GAT3
|
Congenital Disorders of Glycosylation (CDGs)
|
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Temtamy preaxial brachydactyly syndrome
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CHSY1
|
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Congenital Disorders of Glycosylation (CDGs)
|
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Spondyloepiphyseal dysplasia with congenital joint dislocations
|
CHST3
|
|
Congenital Disorders of Glycosylation (CDGs)
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Ehlers-Danlos syndrome, musculocontractural type
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CHST14
|
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Congenital Disorders of Glycosylation (CDGs)
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Partly supported by NIH Common Fund Grant #1U01GM125267-01