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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:13714 | anodontia | HGNC:7159 | Homo sapiens (human) | 4322 | MMP13 |
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| DOID:1067 | open-angle glaucoma | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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| DOID:14115 | toxic shock syndrome | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0111450 | progressive myoclonus epilepsy 9 | HGNC:6638 | Homo sapiens (human) | 84823 | LMNB2 |
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| DOID:1474 | aggressive periodontitis | HGNC:10618 | Homo sapiens (human) | 6347 | CCL2 |
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| DOID:0050572 | cone-rod dystrophy | HGNC:2343 | Homo sapiens (human) | 23418 | CRB1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:53 | Homo sapiens (human) | 1244 | ABCC2 |
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| DOID:10763 | hypertension | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0060058 | lymphoma | HGNC:9955 | Homo sapiens (human) | 5970 | RELA |
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| DOID:0070073 | autosomal dominant intellectual developmental disorder 43 | HGNC:4921 | Homo sapiens (human) | 3097 | HIVEP2 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:9118 | Homo sapiens (human) | 5376 | PMP22 |
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| DOID:0110525 | autosomal recessive nonsyndromic deafness 77 | HGNC:26521 | Homo sapiens (human) | 125336 | LOXHD1 |
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| DOID:5419 | schizophrenia | HGNC:11588 | Homo sapiens (human) | 6908 | TBP |
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| DOID:9119 | acute myeloid leukemia | SGD:S000003060 | Saccharomyces cerevisiae S288C | 852788 | NUP145 |
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| DOID:162 | cancer | SGD:S000001085 | Saccharomyces cerevisiae S288C | 856439 | DOG2 |
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| DOID:1324 | lung cancer | SGD:S000001411 | Saccharomyces cerevisiae S288C | 854657 | MLP2 |
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| DOID:1485 | cystic fibrosis | SGD:S000001692 | Saccharomyces cerevisiae S288C | 853671 | STE6 |
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| DOID:1485 | cystic fibrosis | SGD:S000003513 | Saccharomyces cerevisiae S288C | 853198 | YOR1 |
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| DOID:0112202 | developmental and epileptic encephalopathy | SGD:S000001709 | Saccharomyces cerevisiae S288C | 853870 | VPS1 |
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| DOID:14330 | Parkinson's disease | SGD:S000005113 | Saccharomyces cerevisiae S288C | 855552 | PSD1 |
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| DOID:2476 | hereditary spastic paraplegia | SGD:S000005691 | Saccharomyces cerevisiae S288C | 854336 | SEY1 |
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| DOID:0111446 | progressive myoclonus epilepsy 3 | SGD:S000005569 | Saccharomyces cerevisiae S288C | 854208 | WHI2 |
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| DOID:162 | cancer | SGD:S000001542 | Saccharomyces cerevisiae S288C | 853806 | MPE1 |
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| DOID:14791 | Leber congenital amaurosis | SGD:S000005772 | Saccharomyces cerevisiae S288C | 854420 | ENV9 |
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| DOID:14330 | Parkinson's disease | SGD:S000003394 | Saccharomyces cerevisiae S288C | 853071 | TIF4631 |
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