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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:4783 | mesangial proliferative glomerulonephritis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:10941 | intracranial aneurysm | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:0111054 | von Willebrand's disease 3 | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:3312 | bipolar disorder | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:3770 | pulmonary fibrosis | HGNC:12726 | Homo sapiens (human) | 7450 | VWF |
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| DOID:0111212 | autosomal dominant distal hereditary motor neuronopathy 9 | HGNC:12729 | Homo sapiens (human) | 7453 | WARS1 |
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| DOID:10273 | heart conduction disease | MGI:1921821 | Mus musculus (house mouse) | 74571 | Kcnk16 |
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| DOID:114 | heart disease | MGI:1921821 | Mus musculus (house mouse) | 74571 | Kcnk16 |
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| DOID:1826 | epilepsy | MGI:1921821 | Mus musculus (house mouse) | 74571 | Kcnk16 |
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| DOID:1928 | Williams-Beuren syndrome | HGNC:12741 | Homo sapiens (human) | 7458 | EIF4H |
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| DOID:0060712 | autosomal recessive congenital ichthyosis 4A | MGI:2676312 | Mus musculus (house mouse) | 74591 | Abca12 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | MGI:2676312 | Mus musculus (house mouse) | 74591 | Abca12 |
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| DOID:0060656 | autosomal recessive congenital ichthyosis 1 | MGI:2676312 | Mus musculus (house mouse) | 74591 | Abca12 |
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| DOID:1928 | Williams-Beuren syndrome | HGNC:2586 | Homo sapiens (human) | 7461 | CLIP2 |
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| DOID:0112381 | muscular dystrophy-dystroglycanopathy type C12 | MGI:1921903 | Mus musculus (house mouse) | 74653 | Pomk |
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| DOID:10908 | hydrocephalus | MGI:1921903 | Mus musculus (house mouse) | 74653 | Pomk |
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| DOID:0111235 | congenital muscular dystrophy-dystroglycanopathy type A12 | MGI:1921903 | Mus musculus (house mouse) | 74653 | Pomk |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:11832 | visual epilepsy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:10603 | glucose intolerance | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:5723 | optic atrophy | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:0110584 | autosomal dominant nonsyndromic deafness 6 | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:83 | cataract | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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