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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:5844 | myocardial infarction | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:9778 | irritable bowel syndrome | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:1574 | alcohol use disorder | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:3393 | coronary artery disease | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:557 | kidney disease | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:783 | end stage renal disease | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:12744 | Homo sapiens (human) | 51085 | MLXIPL |
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| DOID:1928 | Williams-Beuren syndrome | HGNC:12741 | Homo sapiens (human) | 7458 | EIF4H |
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| DOID:3310 | atopic dermatitis | HGNC:12735 | Homo sapiens (human) | 8976 | WASL |
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| DOID:9169 | Wiskott-Aldrich syndrome | HGNC:12735 | Homo sapiens (human) | 8976 | WASL |
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| DOID:700 | mitochondrial metabolism disease | HGNC:12730 | Homo sapiens (human) | 10352 | WARS2 |
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| DOID:0111212 | autosomal dominant distal hereditary motor neuronopathy 9 | HGNC:12729 | Homo sapiens (human) | 7453 | WARS1 |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:2217 | Bernard-Soulier syndrome | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:783 | end stage renal disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:0060573 | von Willebrand's disease 1 | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:0060224 | atrial fibrillation | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:10159 | osteonecrosis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:0060574 | von Willebrand's disease 2 | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:5419 | schizophrenia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:4450 | renal cell carcinoma | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:6432 | pulmonary hypertension | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:3407 | carotid artery disease | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:224 | transient cerebral ischemia | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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