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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:0111706 | oblique facial clefting 1 | MGI:1921642 | Mus musculus (house mouse) | 74392 | Specc1l |
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| DOID:674 | cleft palate | MGI:1921642 | Mus musculus (house mouse) | 74392 | Specc1l |
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| DOID:0080698 | Teebi hypertelorism syndrome 1 | MGI:1921642 | Mus musculus (house mouse) | 74392 | Specc1l |
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| DOID:0050567 | orofacial cleft | MGI:1921642 | Mus musculus (house mouse) | 74392 | Specc1l |
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| DOID:5844 | myocardial infarction | HGNC:12716 | Homo sapiens (human) | 7442 | TRPV1 |
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| DOID:6364 | migraine | HGNC:12716 | Homo sapiens (human) | 7442 | TRPV1 |
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| DOID:2548 | reflex epilepsy | HGNC:12716 | Homo sapiens (human) | 7442 | TRPV1 |
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| DOID:0060340 | ciliopathy | MGI:1921727 | Mus musculus (house mouse) | 74477 | 4933427D14Rik |
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| DOID:0050777 | Joubert syndrome | MGI:1921727 | Mus musculus (house mouse) | 74477 | 4933427D14Rik |
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| DOID:0050592 | asphyxiating thoracic dystrophy | MGI:1921727 | Mus musculus (house mouse) | 74477 | 4933427D14Rik |
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| DOID:4501 | orofaciodigital syndrome | MGI:1921727 | Mus musculus (house mouse) | 74477 | 4933427D14Rik |
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| DOID:576 | proteinuria | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:12132 | granulomatosis with polyangiitis | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:8947 | diabetic retinopathy | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:3049 | Churg-Strauss syndrome | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:0060903 | thrombosis | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:3393 | coronary artery disease | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:11832 | visual epilepsy | HGNC:12724 | Homo sapiens (human) | 7448 | VTN |
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| DOID:0080807 | autosomal dominant craniodiaphyseal dysplasia | MGI:1921749 | Mus musculus (house mouse) | 74499 | Sost |
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| DOID:0060756 | sclerosteosis 1 | MGI:1921749 | Mus musculus (house mouse) | 74499 | Sost |
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| DOID:0060251 | sclerosteosis | MGI:1921749 | Mus musculus (house mouse) | 74499 | Sost |
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| DOID:0080036 | SOST-related sclerosing bone dysplasia | MGI:1921749 | Mus musculus (house mouse) | 74499 | Sost |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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| DOID:3526 | cerebral infarction | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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| DOID:1405 | primary angle-closure glaucoma | HGNC:1181 | Homo sapiens (human) | 745 | MYRF |
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