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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:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | HGNC:9202 | Homo sapiens (human) | 10585 | POMT1 |
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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:1508 | candidiasis | HGNC:4020 | Homo sapiens (human) | 10690 | FUT9 |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7056 | Homo sapiens (human) | 10724 | OGA |
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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:576 | proteinuria | MGI:894701 | Mus musculus (house mouse) | 107895 | Mgat5 |
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| DOID:0110312 | hypertrophic cardiomyopathy 6 | MGI:1336153 | Mus musculus (house mouse) | 108099 | Prkag2 |
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| 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:0050571 | congenital disorder of glycosylation type II | MGI:894694 | Mus musculus (house mouse) | 108148 | Galnt2 |
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| DOID:9351 | diabetes mellitus | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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| DOID:0080240 | non-syndromic X-linked intellectual disability 106 | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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| DOID:6000 | congestive heart failure | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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| DOID:1712 | aortic valve stenosis | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1339639 | Mus musculus (house mouse) | 108155 | Ogt |
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| DOID:10652 | Alzheimer's disease | HGNC:2641 | Homo sapiens (human) | 10858 | CYP46A1 |
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| DOID:2377 | multiple sclerosis | Xenbase:XB-GENE-17343520 | Xenopus laevis (African clawed frog) | 108695277 | b4galt6.S |
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