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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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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:11832 | visual epilepsy | HGNC:13448 | Homo sapiens (human) | 54407 | SLC38A2 |
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| DOID:11832 | visual epilepsy | HGNC:13447 | Homo sapiens (human) | 81539 | SLC38A1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:13447 | Homo sapiens (human) | 81539 | SLC38A1 |
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| DOID:0060611 | abdominal obesity-metabolic syndrome | HGNC:13446 | Homo sapiens (human) | 56606 | SLC2A9 |
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| DOID:1920 | hyperuricemia | HGNC:13446 | Homo sapiens (human) | 56606 | SLC2A9 |
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| DOID:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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| DOID:0060475 | myoclonic-atonic epilepsy | HGNC:13433 | Homo sapiens (human) | 64221 | ROBO3 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:3310 | atopic dermatitis | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:0111287 | psoriasis 13 | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:12894 | Sjogren's syndrome | HGNC:1343 | Homo sapiens (human) | 10758 | TRAF3IP2 |
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| DOID:0060272 | pontocerebellar hypoplasia type 3 | HGNC:13406 | Homo sapiens (human) | 27445 | PCLO |
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| DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:162 | cancer | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:12305 | Bloch-Sulzberger syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:13394 | Homo sapiens (human) | 7827 | NPHS2 |
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| DOID:10976 | membranous glomerulonephritis | HGNC:13394 | Homo sapiens (human) | 7827 | NPHS2 |
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| DOID:1184 | nephrotic syndrome | HGNC:13394 | Homo sapiens (human) | 7827 | NPHS2 |
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| DOID:576 | proteinuria | HGNC:13394 | Homo sapiens (human) | 7827 | NPHS2 |
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| DOID:2921 | glomerulonephritis | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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| DOID:783 | end stage renal disease | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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| DOID:576 | proteinuria | HGNC:1339 | Homo sapiens (human) | 729 | C6 |
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