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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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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:0090101 | lethal congenital glycogen storage disease of heart | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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| DOID:384 | Wolff-Parkinson-White syndrome | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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| DOID:2747 | glycogen storage disease | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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| DOID:1289 | neurodegenerative disease | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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| DOID:576 | proteinuria | MGI:894701 | Mus musculus (house mouse) | 107895 | Mgat5 |
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| DOID:1936 | atherosclerosis | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
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| DOID:3181 | oligodendroglioma | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
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| DOID:1612 | breast cancer | HGNC:16049 | Homo sapiens (human) | 10728 | PTGES3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7056 | Homo sapiens (human) | 10724 | OGA |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:1508 | candidiasis | HGNC:4020 | Homo sapiens (human) | 10690 | FUT9 |
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| DOID:2581 | chondrodysplasia punctata | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0111865 | MEND syndrome | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:9884 | muscular dystrophy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:9296 | cleft lip | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050700 | cardiomyopathy | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050453 | lissencephaly | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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| DOID:0060577 | 3MC syndrome 3 | HGNC:2220 | Homo sapiens (human) | 10584 | COLEC10 |
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