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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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:0080855 | Parkinsonism | MGI:104615 | Mus musculus (house mouse) | 12801 | Cnr1 |
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| DOID:10763 | hypertension | MGI:104615 | Mus musculus (house mouse) | 12801 | Cnr1 |
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| DOID:2234 | focal epilepsy | MGI:104615 | Mus musculus (house mouse) | 12801 | Cnr1 |
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| DOID:1824 | status epilepticus | MGI:104615 | Mus musculus (house mouse) | 12801 | Cnr1 |
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| DOID:1875 | impotence | MGI:104615 | Mus musculus (house mouse) | 12801 | Cnr1 |
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| DOID:11830 | myopia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:674 | cleft palate | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0111348 | multiple epiphyseal dysplasia with myopia and deafness | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080676 | Stickler syndrome 1 | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:14789 | spondyloepiphyseal dysplasia congenita | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0112281 | spondyloepiphyseal dysplasia Stanescu type | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:10159 | osteonecrosis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0111508 | Torrance type platyspondylic dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080027 | spondyloepimetaphyseal dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:8398 | osteoarthritis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080046 | Stickler syndrome | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080045 | Kniest dysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:3371 | chondrosarcoma | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:5327 | retinal detachment | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:8886 | chorioretinitis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:1123 | spondyloarthropathy | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:14415 | Legg-Calve-Perthes disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:90 | degenerative disc disease | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:0080044 | hypochondrogenesis | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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| DOID:2256 | osteochondrodysplasia | HGNC:2200 | Homo sapiens (human) | 1280 | COL2A1 |
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