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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:0110841 | Usher syndrome type 3A | HGNC:12605 | Homo sapiens (human) | 7401 | CLRN1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0050144 | Kartagener syndrome | HGNC:2942 | Homo sapiens (human) | 8701 | DNAH11 |
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| DOID:0050453 | lissencephaly | MGI:101864 | Mus musculus (house mouse) | 13138 | Dag1 |
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| DOID:0111030 | hemochromatosis type 3 | MGI:1354956 | Mus musculus (house mouse) | 50765 | Tfr2 |
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| DOID:5394 | prolactinoma | HGNC:9445 | Homo sapiens (human) | 5617 | PRL |
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| DOID:1928 | Williams-Beuren syndrome | MGI:104572 | Mus musculus (house mouse) | 16885 | Limk1 |
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| DOID:14330 | Parkinson's disease | RGD:3729 | Rattus norvegicus (Norway rat) | 29219 | Snca |
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| DOID:0110143 | Bartter disease type 2 | MGI:1927248 | Mus musculus (house mouse) | 56379 | Kcnj1 |
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| DOID:0050790 | fibular hypoplasia and complex brachydactyly | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:9631 | Pelger-Huet anomaly | HGNC:6518 | Homo sapiens (human) | 3930 | LBR |
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| DOID:684 | hepatocellular carcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0050439 | Usher syndrome | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:0110827 | Usher syndrome type 2 | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0050534 | congenital stationary night blindness | HGNC:1393 | Homo sapiens (human) | 778 | CACNA1F |
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| DOID:0050328 | congenital hypothyroidism | HGNC:13273 | Homo sapiens (human) | 50506 | DUOX2 |
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| DOID:9206 | Barrett's esophagus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:83 | cataract | HGNC:5227 | Homo sapiens (human) | 3299 | HSF4 |
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| DOID:784 | chronic kidney disease | RGD:2070 | Rattus norvegicus (Norway rat) | 24180 | Agtr1a |
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| DOID:0050954 | spinocerebellar ataxia type 1 | MGI:104783 | Mus musculus (house mouse) | 20238 | Atxn1 |
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| DOID:12918 | thromboangiitis obliterans | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:783 | end stage renal disease | RGD:3645 | Rattus norvegicus (Norway rat) | 24770 | Ccl2 |
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| DOID:2394 | ovarian cancer | HGNC:6210 | Homo sapiens (human) | 3732 | CD82 |
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| DOID:0080119 | mitochondrial DNA depletion syndrome 1 | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:10763 | hypertension | RGD:728890 | Rattus norvegicus (Norway rat) | 302668 | Ace2 |
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