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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Metachromatic leukodystrophy, due to saposin B deficiency
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PSAP
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Lysosomal Storage Diseases (LSDs)
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Combined saposin deficiency
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PSAP
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Lysosomal Storage Diseases (LSDs)
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POMT1/POMT2-CDG (cong. muscular dystrophy spectrum)
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POMT1,POMT2
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Congenital Disorders of Glycosylation (CDGs)
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POMGNT1-CDG (cong. muscular dystrophy spectrum)
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POMGNT1
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Congenital Disorders of Glycosylation (CDGs)
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PMM2-CDG
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PMM2
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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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Lysyl hydroxylase 3 deficiency
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PLOD3
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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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Partly supported by NIH Common Fund Grant #1U01GM125267-01