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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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Repository for lectin-assisted multimodality data
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MIRAGE
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:0060903 | thrombosis | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:2219 | Glanzmann's thrombasthenia | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:3891 | placental insufficiency | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:1588 | thrombocytopenia | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:10003 | sensorineural hearing loss | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:13514 | venous tributary occlusion of retina | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0060574 | von Willebrand's disease 2 | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:1727 | retinal vein occlusion | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:3393 | coronary artery disease | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0060573 | von Willebrand's disease 1 | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:2349 | arteriosclerosis | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:13241 | Behcet's disease | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:11758 | iron deficiency anemia | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:5844 | myocardial infarction | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:9351 | diabetes mellitus | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:8947 | diabetic retinopathy | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:8805 | intermediate coronary syndrome | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:1612 | breast cancer | HGNC:6134 | Homo sapiens (human) | 3672 | ITGA1 |
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| DOID:10914 | amnestic disorder | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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| DOID:13223 | uterine fibroid | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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| DOID:3393 | coronary artery disease | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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| DOID:4194 | glucose metabolism disease | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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| DOID:10652 | Alzheimer's disease | HGNC:6125 | Homo sapiens (human) | 3667 | IRS1 |
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