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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:5409 | lung small cell carcinoma | HGNC:172 | Homo sapiens (human) | 91 | ACVR1B |
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| DOID:0060387 | chondrodysplasia Blomstrand type | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:0060386 | Chilblain lupus | HGNC:15925 | Homo sapiens (human) | 25939 | SAMHD1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0060767 | autosomal dominant Robinow syndrome 3 | HGNC:3087 | Homo sapiens (human) | 1857 | DVL3 |
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| DOID:13241 | Behcet's disease | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:1936 | atherosclerosis | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:2377 | multiple sclerosis | HGNC:609 | Homo sapiens (human) | 344 | APOC2 |
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| DOID:1588 | thrombocytopenia | HGNC:6138 | Homo sapiens (human) | 3674 | ITGA2B |
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| DOID:2256 | osteochondrodysplasia | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:1883 | hepatitis C | HGNC:5432 | Homo sapiens (human) | 3454 | IFNAR1 |
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| DOID:9663 | aphthous stomatitis | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:1596 | depressive disorder | HGNC:896 | Homo sapiens (human) | 553 | AVPR1B |
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| DOID:0080460 | developmental and epileptic encephalopathy 34 | HGNC:13818 | Homo sapiens (human) | 57468 | SLC12A5 |
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| DOID:0081378 | amyotrophic lateral sclerosis type 24 | HGNC:7744 | Homo sapiens (human) | 4750 | NEK1 |
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| DOID:1283 | enterocele | HGNC:9722 | Homo sapiens (human) | 5832 | ALDH18A1 |
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| DOID:612 | primary immunodeficiency disease | HGNC:23357 | Homo sapiens (human) | 28985 | MCTS1 |
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| DOID:12971 | hereditary spherocytosis | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:9970 | obesity | HGNC:967 | Homo sapiens (human) | 583 | BBS2 |
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| DOID:4959 | epidermolysis bullosa dystrophica | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:9383 | iridocyclitis | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:2043 | hepatitis B | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:10941 | intracranial aneurysm | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:13774 | Addison's disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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