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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:0060488 | Pitt-Hopkins syndrome | MGI:98506 | Mus musculus (house mouse) | 21413 | Tcf4 |
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| DOID:0111459 | classic galactosemia | FB:FBgn0263200 | Drosophila melanogaster (fruit fly) | 33935 | Galt |
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| DOID:3347 | osteosarcoma | RGD:3889 | Rattus norvegicus (Norway rat) | 24842 | Tp53 |
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| DOID:14500 | fucosidosis | MGI:95593 | Mus musculus (house mouse) | 71665 | Fuca1 |
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| DOID:4724 | brain edema | HGNC:633 | Homo sapiens (human) | 358 | AQP1 |
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| DOID:0070489 | classic dopamine transporter deficiency syndrome | FB:FBgn0034136 | Drosophila melanogaster (fruit fly) | 36849 | DAT |
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| DOID:0112247 | congenital heart defects, dysmorphic facial features, and intellectual developmental disorder | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:10763 | hypertension | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:3070 | high grade glioma | SGD:S000004164 | Saccharomyces cerevisiae S288C | 850871 | IDP2 |
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| DOID:3070 | high grade glioma | SGD:S000002224 | Saccharomyces cerevisiae S288C | 851493 | IDP1 |
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| DOID:0110144 | Bartter disease type 3 | MGI:1930643 | Mus musculus (house mouse) | 56365 | Clcnkb |
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| DOID:9351 | diabetes mellitus | HGNC:5465 | Homo sapiens (human) | 3480 | IGF1R |
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| DOID:0050560 | Walker-Warburg syndrome | SGD:S000003904 | Saccharomyces cerevisiae S288C | 853608 | PMT4 |
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| DOID:893 | Wilson disease | RGD:2179 | Rattus norvegicus (Norway rat) | 24941 | Atp7a |
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| DOID:10591 | pre-eclampsia | HGNC:8760 | Homo sapiens (human) | 5133 | PDCD1 |
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| DOID:0080417 | developmental and epileptic encephalopathy 38 | SGD:S000004232 | Saccharomyces cerevisiae S288C | 850943 | ARV1 |
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| DOID:1094 | attention deficit hyperactivity disorder | MGI:2441950 | Mus musculus (house mouse) | 319387 | Adgrl3 |
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| DOID:0111731 | familial episodic pain syndrome 3 | MGI:1345149 | Mus musculus (house mouse) | 24046 | Scn11a |
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| DOID:0060574 | von Willebrand's disease 2 | MGI:98941 | Mus musculus (house mouse) | 22371 | Vwf |
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| DOID:0110081 | arrhythmogenic right ventricular dysplasia 10 | MGI:1196466 | Mus musculus (house mouse) | 13511 | Dsg2 |
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| DOID:0110125 | Bardet-Biedl syndrome 3 | MGI:1927136 | Mus musculus (house mouse) | 56297 | Arl6 |
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| DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:707 | B-cell lymphoma | MGI:107940 | Mus musculus (house mouse) | 14056 | Ezh2 |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | MGI:87868 | Mus musculus (house mouse) | 11409 | Acads |
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