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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:14365 | systemic primary carnitine deficiency disease | MGI:1329012 | Mus musculus (house mouse) | 20520 | Slc22a5 |
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| DOID:0110078 | Leber congenital amaurosis 1 | MGI:105123 | Mus musculus (house mouse) | 14919 | Gucy2e |
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| DOID:0110918 | hereditary spherocytosis type 3 | MGI:98385 | Mus musculus (house mouse) | 20739 | Spta1 |
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| DOID:0050545 | visceral heterotaxy | MGI:106676 | Mus musculus (house mouse) | 22773 | Zic3 |
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| DOID:0110867 | congenital stationary night blindness 1C | MGI:1330305 | Mus musculus (house mouse) | 17364 | Trpm1 |
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| DOID:9074 | systemic lupus erythematosus | MGI:95484 | Mus musculus (house mouse) | 14102 | Fas |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | MGI:95484 | Mus musculus (house mouse) | 14102 | Fas |
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| DOID:6688 | autoimmune lymphoproliferative syndrome | MGI:99255 | Mus musculus (house mouse) | 14103 | Fasl |
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| DOID:0090140 | cortisone reductase deficiency 2 | MGI:103562 | Mus musculus (house mouse) | 15483 | Hsd11b1 |
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| DOID:10763 | hypertension | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:10652 | Alzheimer's disease | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:13994 | cleidocranial dysplasia | MGI:99829 | Mus musculus (house mouse) | 12393 | Runx2 |
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| DOID:12308 | Dubin-Johnson syndrome | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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| DOID:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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| DOID:13481 | thanatophoric dysplasia | HGNC:3690 | Homo sapiens (human) | 2261 | FGFR3 |
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| DOID:1588 | thrombocytopenia | HGNC:7217 | Homo sapiens (human) | 4352 | MPL |
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| DOID:0070247 | autosomal dominant Emery-Dreifuss muscular dystrophy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0060439 | lysinuric protein intolerance | HGNC:11065 | Homo sapiens (human) | 9056 | SLC7A7 |
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| DOID:2217 | Bernard-Soulier syndrome | HGNC:4439 | Homo sapiens (human) | 2811 | GP1BA |
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| DOID:0060601 | alpha-2-plasmin inhibitor deficiency | MGI:107173 | Mus musculus (house mouse) | 18816 | Serpinf2 |
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| DOID:2741 | bilirubin metabolic disorder | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:3883 | Lynch syndrome | MGI:101938 | Mus musculus (house mouse) | 17350 | Mlh1 |
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| DOID:14323 | Marfan syndrome | MGI:95489 | Mus musculus (house mouse) | 14118 | Fbn1 |
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| DOID:10652 | Alzheimer's disease | MGI:88059 | Mus musculus (house mouse) | 11820 | App |
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| DOID:576 | proteinuria | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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