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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0050453 | lissencephaly | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0080737 | Ehlers-Danlos syndrome musculocontractural type 2 | HGNC:21144 | Homo sapiens (human) | 29940 | DSE |
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| DOID:0080555 | congenital disorder of glycosylation Ic | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:0112321 | alacrima, achalasia, and impaired intellectual development syndrome | HGNC:22923 | Homo sapiens (human) | 29926 | GMPPA |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0112377 | muscular dystrophy-dystroglycanopathy type B14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:2747 | glycogen storage disease | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:0050579 | glycogen storage disease XV | HGNC:4699 | Homo sapiens (human) | 2992 | GYG1 |
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| DOID:8283 | peritonitis | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:12803 | Sly syndrome | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:12798 | mucopolysaccharidosis | HGNC:4696 | Homo sapiens (human) | 2990 | GUSB |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0080322 | polycystic kidney disease | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | RGD:1309558 | Rattus norvegicus (Norway rat) | 298690 | B3galt6 |
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| DOID:13359 | Ehlers-Danlos syndrome | RGD:1309558 | Rattus norvegicus (Norway rat) | 298690 | B3galt6 |
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| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | RGD:1309558 | Rattus norvegicus (Norway rat) | 298690 | B3galt6 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1353418 | Mus musculus (house mouse) | 29858 | Pmm1 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | MGI:1353418 | Mus musculus (house mouse) | 29858 | Pmm1 |
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| DOID:0111459 | classic galactosemia | RGD:1306483 | Rattus norvegicus (Norway rat) | 298003 | Galt |
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| DOID:9870 | galactosemia | RGD:1306483 | Rattus norvegicus (Norway rat) | 298003 | Galt |
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| DOID:8893 | psoriasis | RGD:631365 | Rattus norvegicus (Norway rat) | 297508 | Nampt |
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