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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:10811 | nasal cavity cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0112368 | Coffin-Siris syndrome 5 | HGNC:11109 | Homo sapiens (human) | 6605 | SMARCE1 |
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| DOID:0090131 | complex cortical dysplasia with other brain malformations | HGNC:19946 | Homo sapiens (human) | 157922 | CAMSAP1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:6011 | Homo sapiens (human) | 3562 | IL3 |
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| DOID:0050591 | tooth agenesis | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:12930 | dilated cardiomyopathy | HGNC:3331 | Homo sapiens (human) | 2010 | EMD |
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| DOID:14330 | Parkinson's disease | HGNC:11960 | Homo sapiens (human) | 26058 | GIGYF2 |
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| DOID:0081179 | autosomal recessive intellectual developmental disorder 3 | HGNC:30237 | Homo sapiens (human) | 54862 | CC2D1A |
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| DOID:2316 | brain ischemia | HGNC:9051 | Homo sapiens (human) | 5327 | PLAT |
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| DOID:0050788 | proximal symphalangism | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:2841 | asthma | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:6243 | Homo sapiens (human) | 10008 | KCNE3 |
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| DOID:1070 | primary open angle glaucoma | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:13241 | Behcet's disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0111498 | combined oxidative phosphorylation deficiency 22 | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:0050663 | Bethlem myopathy | HGNC:2212 | Homo sapiens (human) | 1292 | COL6A2 |
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| DOID:9970 | obesity | RGD:61861 | Rattus norvegicus (Norway rat) | 29708 | Gabra6 |
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| DOID:0111298 | familial febrile seizures 8 | HGNC:4087 | Homo sapiens (human) | 2566 | GABRG2 |
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| DOID:2033 | communication disorder | HGNC:2717 | Homo sapiens (human) | 1642 | DDB1 |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:3121 | gallbladder cancer | HGNC:6693 | Homo sapiens (human) | 53353 | LRP1B |
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| DOID:0111849 | osteogenesis imperfecta type 20 | HGNC:13520 | Homo sapiens (human) | 23184 | MESD |
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| DOID:9538 | multiple myeloma | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:14711 | FG syndrome | HGNC:1497 | Homo sapiens (human) | 8573 | CASK |
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