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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:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:11199 | hypoparathyroidism | HGNC:11582 | Homo sapiens (human) | 6905 | TBCE |
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| DOID:0050073 | invasive aspergillosis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:10534 | stomach cancer | HGNC:6307 | Homo sapiens (human) | 3791 | KDR |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:3691 | Homo sapiens (human) | 2264 | FGFR4 |
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| DOID:2377 | multiple sclerosis | HGNC:1653 | Homo sapiens (human) | 940 | CD28 |
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| DOID:2841 | asthma | HGNC:2358 | Homo sapiens (human) | 1395 | CRHR2 |
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| DOID:0080822 | aspirin-induced respiratory disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:1588 | thrombocytopenia | HGNC:11283 | Homo sapiens (human) | 6714 | SRC |
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| DOID:0110831 | Usher syndrome type 1D | HGNC:14674 | Homo sapiens (human) | 65217 | PCDH15 |
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| DOID:0080688 | mosaic variegated aneuploidy syndrome | HGNC:17814 | Homo sapiens (human) | 55719 | SLF2 |
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| DOID:0060752 | familial temporal lobe epilepsy 5 | HGNC:17245 | Homo sapiens (human) | 57094 | CPA6 |
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| DOID:0110682 | congenital myasthenic syndrome 16 | HGNC:10591 | Homo sapiens (human) | 6329 | SCN4A |
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| DOID:8947 | diabetic retinopathy | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:0050742 | nicotine dependence | HGNC:13286 | Homo sapiens (human) | 63979 | FIGNL1 |
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| DOID:9970 | obesity | HGNC:12775 | Homo sapiens (human) | 7480 | WNT10B |
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| DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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| DOID:11829 | degenerative myopia | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0080608 | anterior segment dysgenesis 3 | HGNC:3800 | Homo sapiens (human) | 2296 | FOXC1 |
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| DOID:3393 | coronary artery disease | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:9743 | diabetic neuropathy | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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| DOID:9415 | allergic asthma | HGNC:4933 | Homo sapiens (human) | 3107 | HLA-C |
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| DOID:0112137 | combined oxidative phosphorylation deficiency 51 | HGNC:24717 | Homo sapiens (human) | 55037 | PTCD3 |
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| DOID:936 | brain disease | HGNC:9848 | Homo sapiens (human) | 5903 | RANBP2 |
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