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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:1289 | neurodegenerative disease | HGNC:11854 | Homo sapiens (human) | 7102 | TSPAN7 |
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| DOID:0112024 | non-syndromic X-linked intellectual disability 58 | HGNC:11854 | Homo sapiens (human) | 7102 | TSPAN7 |
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| DOID:14330 | Parkinson's disease | HGNC:11854 | Homo sapiens (human) | 7102 | TSPAN7 |
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| DOID:11725 | Cornelia de Lange syndrome | MGI:1913976 | Mus musculus (house mouse) | 71175 | Nipbl |
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| DOID:162 | cancer | MGI:1913976 | Mus musculus (house mouse) | 71175 | Nipbl |
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| DOID:0080505 | Cornelia de Lange syndrome 1 | MGI:1913976 | Mus musculus (house mouse) | 71175 | Nipbl |
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| DOID:11758 | iron deficiency anemia | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:1826 | epilepsy | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:2921 | glomerulonephritis | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1241 | Homo sapiens (human) | 712 | C1QA |
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| DOID:13300 | Scheuermann's disease | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:8398 | osteoarthritis | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:0070441 | retinal macular dystrophy 4 | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:5419 | schizophrenia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5199 | ureteral obstruction | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4362 | cervical cancer | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:557 | kidney disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:1824 | status epilepticus | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:8947 | diabetic retinopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4483 | rhinitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:824 | periodontitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050697 | chorioamnionitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11963 | esophagitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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