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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:0110646 | long QT syndrome 3 | HGNC:10593 | Homo sapiens (human) | 6331 | SCN5A |
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| DOID:12531 | von Willebrand's disease | MGI:98941 | Mus musculus (house mouse) | 22371 | Vwf |
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| DOID:0080552 | congenital disorder of glycosylation Ia | SGD:S000001849 | Saccharomyces cerevisiae S288C | 850499 | SEC53 |
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| DOID:0060041 | autism spectrum disorder | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:0111722 | amelogenesis imperfecta type 3C | MGI:2443373 | Mus musculus (house mouse) | 320100 | Relt |
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| DOID:0112102 | Sotos syndrome 2 | MGI:97311 | Mus musculus (house mouse) | 18032 | Nfix |
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| DOID:0111403 | mega-corpus-callosum syndrome with cerebellar hypoplasia and cortical malformations | MGI:1861901 | Mus musculus (house mouse) | 56527 | Mast1 |
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| DOID:0060462 | Desbuquois dysplasia | MGI:1923275 | Mus musculus (house mouse) | 76025 | Cant1 |
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| DOID:13884 | sick sinus syndrome | MGI:98251 | Mus musculus (house mouse) | 20271 | Scn5a |
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| DOID:1686 | glaucoma | HGNC:9644 | Homo sapiens (human) | 5781 | PTPN11 |
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| DOID:0111960 | immunodeficiency 15A | MGI:1338071 | Mus musculus (house mouse) | 16150 | Ikbkb |
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| DOID:1574 | alcohol use disorder | HGNC:8023 | Homo sapiens (human) | 4908 | NTF3 |
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| DOID:1574 | alcohol use disorder | HGNC:1033 | Homo sapiens (human) | 627 | BDNF |
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| DOID:0060246 | MASA syndrome | FB:FBgn0264975 | Drosophila melanogaster (fruit fly) | 31792 | Nrg |
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| DOID:0080642 | Middle East respiratory syndrome | HGNC:3009 | Homo sapiens (human) | 1803 | DPP4 |
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| DOID:1588 | thrombocytopenia | SGD:S000000223 | Saccharomyces cerevisiae S288C | 852307 | GAL10 |
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| DOID:10584 | retinitis pigmentosa | ZFIN:ZDB-GENE-990415-271 | Danio rerio (zebrafish) | 30295 | rho |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:3373 | Homo sapiens (human) | 2033 | EP300 |
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| DOID:0050156 | idiopathic pulmonary fibrosis | HGNC:2730 | Homo sapiens (human) | 780 | DDR1 |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | MGI:1352630 | Mus musculus (house mouse) | 20928 | Abcc9 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6430 | Homo sapiens (human) | 3875 | KRT18 |
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| DOID:0060900 | Parkinson's disease 14 | MGI:1859152 | Mus musculus (house mouse) | 53357 | Pla2g6 |
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| DOID:13133 | HELLP syndrome | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:13133 | HELLP syndrome | HGNC:11936 | Homo sapiens (human) | 356 | FASLG |
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| DOID:0050475 | Weill-Marchesani syndrome | MGI:2449112 | Mus musculus (house mouse) | 224697 | Adamts10 |
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