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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:8778 | Crohn's disease | HGNC:1095 | Homo sapiens (human) | 671 | BPI |
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| DOID:3620 | central nervous system cancer | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0060060 | non-Hodgkin lymphoma | HGNC:6819 | Homo sapiens (human) | 10892 | MALT1 |
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| DOID:0050905 | inflammatory myofibroblastic tumor | HGNC:9848 | Homo sapiens (human) | 5903 | RANBP2 |
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| DOID:0111108 | maturity-onset diabetes of the young type 10 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:0080326 | familial hypertrophic cardiomyopathy | HGNC:19012 | Homo sapiens (human) | 10699 | CORIN |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:0080625 | severe congenital neutropenia 1 | HGNC:3309 | Homo sapiens (human) | 1991 | ELANE |
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| DOID:10873 | Kuhnt-Junius degeneration | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:0050432 | Asperger syndrome | HGNC:10982 | Homo sapiens (human) | 8604 | SLC25A12 |
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| DOID:0050745 | diffuse large B-cell lymphoma | HGNC:6006 | Homo sapiens (human) | 50615 | IL21R |
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| DOID:11054 | urinary bladder cancer | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:83 | cataract | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:12361 | Graves' disease | HGNC:6011 | Homo sapiens (human) | 3562 | IL3 |
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| DOID:2468 | psychotic disorder | HGNC:7997 | Homo sapiens (human) | 3084 | NRG1 |
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| DOID:0050465 | Muir-Torre syndrome | HGNC:7325 | Homo sapiens (human) | 4436 | MSH2 |
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| DOID:10283 | prostate cancer | HGNC:3392 | Homo sapiens (human) | 2047 | EPHB1 |
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| DOID:11836 | clubfoot | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:614 | lymphopenia | RGD:2536 | Rattus norvegicus (Norway rat) | 50672 | Ednrb |
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| DOID:13241 | Behcet's disease | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0111821 | ichthyosis follicularis-alopecia-photophobia syndrome 1 | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:8805 | intermediate coronary syndrome | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:684 | hepatocellular carcinoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:6189 | Homo sapiens (human) | 3714 | JAG2 |
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