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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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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:0060573 | von Willebrand's disease 1 | MGI:97610 | Mus musculus (house mouse) | 18791 | Plat |
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| DOID:0060573 | von Willebrand's disease 1 | RGD:3342 | Rattus norvegicus (Norway rat) | 25692 | Plat |
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| DOID:0060573 | von Willebrand's disease 1 | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0060573 | von Willebrand's disease 1 | WB:WBGene00003929 | Caenorhabditis elegans | 176240 | pat-2 |
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| DOID:0060573 | von Willebrand's disease 1 | HGNC:6138 | Homo sapiens (human) | 3674 | ITGA2B |
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| DOID:0060572 | Ritscher-Schinzel syndrome 2 | HGNC:28909 | Homo sapiens (human) | 28952 | CCDC22 |
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| DOID:0060571 | Ritscher-Schinzel syndrome 1 | HGNC:28984 | Homo sapiens (human) | 9897 | WASHC5 |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | RGD:3787 | Rattus norvegicus (Norway rat) | 25560 | Abcc9 |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | SGD:S000003971 | Saccharomyces cerevisiae S288C | 850678 | YBT1 |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | MGI:1352630 | Mus musculus (house mouse) | 20928 | Abcc9 |
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| DOID:0060565 | Ritscher-Schinzel syndrome | MGI:1918767 | Mus musculus (house mouse) | 71517 | Vps35l |
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| DOID:0060565 | Ritscher-Schinzel syndrome | HGNC:24641 | Homo sapiens (human) | 57020 | VPS35L |
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| DOID:0060565 | Ritscher-Schinzel syndrome | MGI:1929772 | Mus musculus (house mouse) | 65254 | Dpysl5 |
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| DOID:0060564 | spinal disease | MGI:104629 | Mus musculus (house mouse) | 18619 | Penk |
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| DOID:0060564 | spinal disease | MGI:1929183 | Mus musculus (house mouse) | 64930 | Tsc1 |
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| DOID:0060564 | spinal disease | RGD:68946 | Rattus norvegicus (Norway rat) | 29237 | Penk |
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| DOID:0060564 | spinal disease | HGNC:12362 | Homo sapiens (human) | 7248 | TSC1 |
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| DOID:0060564 | spinal disease | MGI:2446089 | Mus musculus (house mouse) | 286940 | Flnb |
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| DOID:0060564 | spinal disease | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0060563 | Char syndrome | MGI:104672 | Mus musculus (house mouse) | 21419 | Tfap2b |
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| DOID:0060563 | Char syndrome | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:0060560 | lethal congenital contracture syndrome 2 | MGI:95411 | Mus musculus (house mouse) | 13867 | Erbb3 |
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| DOID:0060560 | lethal congenital contracture syndrome 2 | WB:WBGene00002299 | Caenorhabditis elegans | 174462 | let-23 |
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| DOID:0060560 | lethal congenital contracture syndrome 2 | RGD:69323 | Rattus norvegicus (Norway rat) | 29496 | Erbb3 |
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