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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:0080821 | exercise-induced bronchoconstriction | HGNC:11526 | Homo sapiens (human) | 6869 | TACR1 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:9258 | Waardenburg syndrome | HGNC:3180 | Homo sapiens (human) | 1910 | EDNRB |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:6664 | Homo sapiens (human) | 4015 | LOX |
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| DOID:11400 | pyelonephritis | HGNC:6000 | Homo sapiens (human) | 3557 | IL1RN |
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| DOID:422 | congenital structural myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:445 | Bartter disease | HGNC:10910 | Homo sapiens (human) | 6557 | SLC12A1 |
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| DOID:12971 | hereditary spherocytosis | HGNC:492 | Homo sapiens (human) | 286 | ANK1 |
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| DOID:4479 | pseudohypoaldosteronism | HGNC:10602 | Homo sapiens (human) | 6340 | SCNN1G |
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| DOID:3068 | glioblastoma | HGNC:2535 | Homo sapiens (human) | 1512 | CTSH |
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| DOID:3393 | coronary artery disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:10762 | portal hypertension | RGD:2611 | Rattus norvegicus (Norway rat) | 25022 | Fgfr2 |
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| DOID:11198 | DiGeorge syndrome | HGNC:3084 | Homo sapiens (human) | 1855 | DVL1 |
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| DOID:2920 | membranoproliferative glomerulonephritis | RGD:3742 | Rattus norvegicus (Norway rat) | 24791 | Sparc |
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| DOID:8398 | osteoarthritis | HGNC:3778 | Homo sapiens (human) | 2335 | FN1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:11157 | Homo sapiens (human) | 6631 | SNRPC |
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| DOID:0080179 | haemophilus meningitis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:8719 | in situ carcinoma | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:8791 | breast carcinoma in situ | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:700 | mitochondrial metabolism disease | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:0050632 | oculocutaneous albinism | HGNC:12450 | Homo sapiens (human) | 7306 | TYRP1 |
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| DOID:106 | pleural tuberculosis | HGNC:1839 | Homo sapiens (human) | 51816 | ADA2 |
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| DOID:112 | esophageal varix | HGNC:399 | Homo sapiens (human) | 213 | ALB |
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| DOID:12858 | Huntington's disease | HGNC:336 | Homo sapiens (human) | 185 | AGTR1 |
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| DOID:14330 | Parkinson's disease | HGNC:336 | Homo sapiens (human) | 185 | AGTR1 |
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