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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
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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:1967 | leiomyosarcoma | MGI:105062 | Mus musculus (house mouse) | 110542 | Amhr2 |
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| DOID:0080909 | castration-resistant prostate carcinoma | HGNC:1915 | Homo sapiens (human) | 1105 | CHD1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:1915 | Homo sapiens (human) | 1105 | CHD1 |
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| DOID:10283 | prostate cancer | HGNC:1915 | Homo sapiens (human) | 1105 | CHD1 |
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| DOID:3393 | coronary artery disease | MGI:87871 | Mus musculus (house mouse) | 110460 | Acat2 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:5844 | myocardial infarction | MGI:88236 | Mus musculus (house mouse) | 110382 | C8b |
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| DOID:0060302 | type II complement component 8 deficiency | MGI:88236 | Mus musculus (house mouse) | 110382 | C8b |
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| DOID:1909 | melanoma | MGI:109338 | Mus musculus (house mouse) | 110351 | Rap1gap |
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| DOID:3312 | bipolar disorder | MGI:109338 | Mus musculus (house mouse) | 110351 | Rap1gap |
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| DOID:1312 | focal segmental glomerulosclerosis | MGI:109338 | Mus musculus (house mouse) | 110351 | Rap1gap |
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| DOID:3969 | thyroid gland papillary carcinoma | MGI:109338 | Mus musculus (house mouse) | 110351 | Rap1gap |
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| DOID:0050908 | myelodysplastic syndrome | MGI:109338 | Mus musculus (house mouse) | 110351 | Rap1gap |
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| DOID:1793 | pancreatic cancer | MGI:109338 | Mus musculus (house mouse) | 110351 | Rap1gap |
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| DOID:0050563 | nonsyndromic deafness | MGI:107736 | Mus musculus (house mouse) | 110350 | Dync2h1 |
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| DOID:14679 | VACTERL association | MGI:107736 | Mus musculus (house mouse) | 110350 | Dync2h1 |
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| DOID:0050592 | asphyxiating thoracic dystrophy | MGI:107736 | Mus musculus (house mouse) | 110350 | Dync2h1 |
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| DOID:0110087 | asphyxiating thoracic dystrophy 3 | MGI:107736 | Mus musculus (house mouse) | 110350 | Dync2h1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:10021 | Homo sapiens (human) | 11035 | RIPK3 |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:10021 | Homo sapiens (human) | 11035 | RIPK3 |
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| DOID:11984 | hypertrophic cardiomyopathy | MGI:107460 | Mus musculus (house mouse) | 110323 | Cox6b1 |
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| DOID:0070494 | mitochondrial complex IV deficiency nuclear type 7 | MGI:107460 | Mus musculus (house mouse) | 110323 | Cox6b1 |
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| DOID:890 | mitochondrial encephalomyopathy | MGI:107460 | Mus musculus (house mouse) | 110323 | Cox6b1 |
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