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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:0110152 | Charcot-Marie-Tooth disease type 1B | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
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| DOID:0111196 | X-linked distal spinal muscular atrophy 3 | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:0050791 | persistent Mullerian duct syndrome | HGNC:465 | Homo sapiens (human) | 269 | AMHR2 |
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| DOID:2962 | Cockayne syndrome | HGNC:3438 | Homo sapiens (human) | 2074 | ERCC6 |
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| DOID:0070468 | Yoon-Bellen neurodevelopmental syndrome | HGNC:25590 | Homo sapiens (human) | 55753 | OGDHL |
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| DOID:13832 | patent ductus arteriosus | HGNC:11743 | Homo sapiens (human) | 7021 | TFAP2B |
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| DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:11759 | hypochromic anemia | RGD:3684 | Rattus norvegicus (Norway rat) | 25715 | Slc11a2 |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:4883 | Homo sapiens (human) | 3075 | CFH |
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| DOID:0080209 | sideroblastic anemia with B-cell immunodeficiency, periodic fevers, and developmental delay | HGNC:17341 | Homo sapiens (human) | 51095 | TRNT1 |
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| DOID:5844 | myocardial infarction | HGNC:11766 | Homo sapiens (human) | 7040 | TGFB1 |
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| DOID:4795 | GM2 gangliosidosis, AB variant | HGNC:4367 | Homo sapiens (human) | 2760 | GM2A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:428 | Homo sapiens (human) | 7840 | ALMS1 |
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| DOID:0080047 | pseudoachondroplasia | HGNC:2227 | Homo sapiens (human) | 1311 | COMP |
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| DOID:10763 | hypertension | HGNC:14685 | Homo sapiens (human) | 50848 | F11R |
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| DOID:0050742 | nicotine dependence | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:0111102 | maturity-onset diabetes of the young type 3 | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:1168 | familial hyperlipidemia | HGNC:609 | Homo sapiens (human) | 344 | APOC2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:0060234 | Carpenter syndrome | HGNC:3233 | Homo sapiens (human) | 1954 | MEGF8 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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| DOID:0080695 | Burn-McKeown syndrome | HGNC:30551 | Homo sapiens (human) | 10907 | TXNL4A |
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| DOID:0111254 | glutaric acidemia I | HGNC:4189 | Homo sapiens (human) | 2639 | GCDH |
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| DOID:12704 | ataxia telangiectasia | HGNC:795 | Homo sapiens (human) | 472 | ATM |
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| DOID:3317 | hepatic angiomyolipoma | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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