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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:4989 | pancreatitis | MGI:99501 | Mus musculus (house mouse) | 110135 | Fgb |
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| DOID:5844 | myocardial infarction | MGI:99501 | Mus musculus (house mouse) | 110135 | Fgb |
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| DOID:3407 | carotid artery disease | MGI:99501 | Mus musculus (house mouse) | 110135 | Fgb |
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| DOID:2236 | congenital afibrinogenemia | MGI:99501 | Mus musculus (house mouse) | 110135 | Fgb |
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| DOID:1287 | cardiovascular system disease | MGI:99501 | Mus musculus (house mouse) | 110135 | Fgb |
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| DOID:9477 | pulmonary embolism | MGI:99501 | Mus musculus (house mouse) | 110135 | Fgb |
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| DOID:2978 | carbohydrate metabolic disorder | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:0080554 | congenital disorder of glycosylation Ib | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:11842 | Homo sapiens (human) | 11011 | TLK2 |
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| DOID:2754 | glycogen storage disease VI | MGI:97829 | Mus musculus (house mouse) | 110095 | Pygl |
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| DOID:2747 | glycogen storage disease | MGI:97829 | Mus musculus (house mouse) | 110095 | Pygl |
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| DOID:3650 | lactic acidosis | MGI:97829 | Mus musculus (house mouse) | 110095 | Pygl |
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| DOID:0050545 | visceral heterotaxy | MGI:97577 | Mus musculus (house mouse) | 110094 | Phka2 |
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| DOID:0111042 | glycogen storage disease IXa | MGI:97577 | Mus musculus (house mouse) | 110094 | Phka2 |
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| DOID:2747 | glycogen storage disease | MGI:97577 | Mus musculus (house mouse) | 110094 | Phka2 |
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| DOID:3388 | periodontal disease | HGNC:11346 | Homo sapiens (human) | 11009 | IL24 |
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| DOID:9562 | primary ciliary dyskinesia | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:0110599 | primary ciliary dyskinesia 3 | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:10754 | otitis media | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:0050545 | visceral heterotaxy | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:6419 | tetralogy of Fallot | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:0050144 | Kartagener syndrome | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:0112199 | spondyloepimetaphyseal dysplasia with joint laxity type 2 | MGI:109233 | Mus musculus (house mouse) | 110033 | Kif22 |
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| DOID:12803 | Sly syndrome | MGI:95872 | Mus musculus (house mouse) | 110006 | Gusb |
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