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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:1485 | cystic fibrosis | HGNC:18967 | Homo sapiens (human) | 9695 | EDEM1 |
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| DOID:0111743 | cerebellar ataxia type 47 | HGNC:14957 | Homo sapiens (human) | 9698 | PUM1 |
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| DOID:9970 | obesity | HGNC:14957 | Homo sapiens (human) | 9698 | PUM1 |
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| DOID:5419 | schizophrenia | HGNC:17283 | Homo sapiens (human) | 9699 | RIMS2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:17283 | Homo sapiens (human) | 9699 | RIMS2 |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:11937 | Homo sapiens (human) | 970 | CD70 |
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| DOID:0080142 | mosaic variegated aneuploidy syndrome 2 | HGNC:30794 | Homo sapiens (human) | 9702 | CEP57 |
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| DOID:585 | nephrolithiasis | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:305 | carcinoma | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:114 | heart disease | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:12712 | nephronophthisis | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:1289 | neurodegenerative disease | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:162 | cancer | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:10155 | intestinal cancer | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:2394 | ovarian cancer | MGI:1917649 | Mus musculus (house mouse) | 97064 | Wwtr1 |
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| DOID:1875 | impotence | HGNC:14631 | Homo sapiens (human) | 9719 | ADAMTSL2 |
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| DOID:0111725 | geleophysic dysplasia 1 | HGNC:14631 | Homo sapiens (human) | 9719 | ADAMTSL2 |
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| DOID:10652 | Alzheimer's disease | MGI:2135593 | Mus musculus (house mouse) | 97212 | Hadha |
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| DOID:0111277 | mitochondrial trifunctional protein deficiency | MGI:2135593 | Mus musculus (house mouse) | 97212 | Hadha |
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| DOID:9452 | steatotic liver disease | MGI:2135593 | Mus musculus (house mouse) | 97212 | Hadha |
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| DOID:3146 | lipid metabolism disorder | MGI:2135593 | Mus musculus (house mouse) | 97212 | Hadha |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:2135593 | Mus musculus (house mouse) | 97212 | Hadha |
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| DOID:0050834 | CHARGE syndrome | HGNC:10727 | Homo sapiens (human) | 9723 | SEMA3E |
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| DOID:224 | transient cerebral ischemia | HGNC:10727 | Homo sapiens (human) | 9723 | SEMA3E |
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| DOID:0070400 | hypomyelinating leukodystrophy 19 | HGNC:29118 | Homo sapiens (human) | 9725 | TMEM63A |
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