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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:0060041 | autism spectrum disorder | MGI:1096391 | Mus musculus (house mouse) | 18189 | Nrxn1 |
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| DOID:10652 | Alzheimer's disease | HGNC:7782 | Homo sapiens (human) | 4780 | NFE2L2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:7794 | Homo sapiens (human) | 4790 | NFKB1 |
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| DOID:0080074 | neural tube defect | HGNC:21055 | Homo sapiens (human) | 25902 | MTHFD1L |
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| DOID:0080505 | Cornelia de Lange syndrome 1 | MGI:1913976 | Mus musculus (house mouse) | 71175 | Nipbl |
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| DOID:0110372 | retinitis pigmentosa 4 | MGI:97914 | Mus musculus (house mouse) | 212541 | Rho |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:9676 | Homo sapiens (human) | 5798 | PTPRN |
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| DOID:0081060 | X-linked nephrogenic diabetes insipidus | MGI:88123 | Mus musculus (house mouse) | 12000 | Avpr2 |
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| DOID:9970 | obesity | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:3070 | high grade glioma | FB:FBgn0283499 | Drosophila melanogaster (fruit fly) | 42549 | InR |
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| DOID:0050430 | multiple endocrine neoplasia type 2A | HGNC:9967 | Homo sapiens (human) | 5979 | RET |
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| DOID:10584 | retinitis pigmentosa | HGNC:30859 | Homo sapiens (human) | 23020 | SNRNP200 |
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| DOID:14330 | Parkinson's disease | RGD:2869 | Rattus norvegicus (Norway rat) | 25718 | Igf1r |
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| DOID:0060748 | familial temporal lobe epilepsy 1 | MGI:1861691 | Mus musculus (house mouse) | 56839 | Lgi1 |
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| DOID:1574 | alcohol use disorder | HGNC:15963 | Homo sapiens (human) | 8973 | CHRNA6 |
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| DOID:11721 | glycogen storage disease VII | MGI:97548 | Mus musculus (house mouse) | 18642 | Pfkm |
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| DOID:5082 | liver cirrhosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060691 | platelet-type bleeding disorder 16 | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | HGNC:6138 | Homo sapiens (human) | 3674 | ITGA2B |
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| DOID:1824 | status epilepticus | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:10591 | pre-eclampsia | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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| DOID:2219 | Glanzmann's thrombasthenia | HGNC:6156 | Homo sapiens (human) | 3690 | ITGB3 |
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| DOID:3770 | pulmonary fibrosis | HGNC:5973 | Homo sapiens (human) | 3596 | IL13 |
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| DOID:0060672 | Grn-related frontotemporal lobar degeneration with Tdp43 inclusions | HGNC:4601 | Homo sapiens (human) | 2896 | GRN |
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| DOID:0110229 | cataract 6 multiple types | MGI:95278 | Mus musculus (house mouse) | 13836 | Epha2 |
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