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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:2043 | hepatitis B | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:10788 | Homo sapiens (human) | 6431 | SRSF6 |
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| DOID:8778 | Crohn's disease | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:0111927 | spermatogenic failure 37 | HGNC:30761 | Homo sapiens (human) | 199223 | TTC21A |
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| DOID:0070430 | combined oxidative phosphorylation deficiency 57 | HGNC:16148 | Homo sapiens (human) | 54675 | CRLS1 |
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| DOID:0110035 | Alzheimer's disease 2 | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0112080 | nuclear type mitochondrial complex I deficiency 32 | HGNC:7703 | Homo sapiens (human) | 4714 | NDUFB8 |
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| DOID:0081341 | congenital myopathy 5 | HGNC:12403 | Homo sapiens (human) | 7273 | TTN |
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| DOID:3310 | atopic dermatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:5844 | myocardial infarction | HGNC:22393 | Homo sapiens (human) | 339479 | BRINP3 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:0080721 | calvarial doughnut lesions with bone fragility | HGNC:28395 | Homo sapiens (human) | 166929 | SGMS2 |
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| DOID:0111625 | ventriculomegaly - cystic kidney disease | HGNC:18688 | Homo sapiens (human) | 286204 | CRB2 |
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| DOID:3393 | coronary artery disease | HGNC:3662 | Homo sapiens (human) | 2244 | FGB |
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| DOID:9409 | diabetes insipidus | RGD:2142 | Rattus norvegicus (Norway rat) | 25386 | Aqp2 |
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| DOID:8577 | ulcerative colitis | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:1962 | fallopian tube disease | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:11054 | urinary bladder cancer | HGNC:7516 | Homo sapiens (human) | 727897 | MUC5B |
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| DOID:0111950 | immunodeficiency 29 | HGNC:5970 | Homo sapiens (human) | 3593 | IL12B |
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| DOID:2986 | IgA glomerulonephritis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:633 | myositis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:2218 | blood platelet disease | HGNC:3393 | Homo sapiens (human) | 2048 | EPHB2 |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:6188 | Homo sapiens (human) | 182 | JAG1 |
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| DOID:8778 | Crohn's disease | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:1936 | atherosclerosis | HGNC:2203 | Homo sapiens (human) | 1284 | COL4A2 |
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