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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:0112247 | congenital heart defects, dysmorphic facial features, and intellectual developmental disorder | MGI:1916812 | Mus musculus (house mouse) | 69562 | Cdk13 |
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| DOID:0081075 | Marsili syndrome | MGI:2686934 | Mus musculus (house mouse) | 239102 | Zfhx2 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | MGI:2445096 | Mus musculus (house mouse) | 209692 | Dhtkd1 |
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| DOID:2211 | factor XIII deficiency | MGI:1921395 | Mus musculus (house mouse) | 74145 | F13a1 |
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| DOID:0111008 | X-linked cone-rod dystrophy 1 | MGI:1344037 | Mus musculus (house mouse) | 19893 | Rpgr |
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| DOID:0060230 | basal ganglia calcification | MGI:97531 | Mus musculus (house mouse) | 18596 | Pdgfrb |
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| DOID:8893 | psoriasis | MGI:103038 | Mus musculus (house mouse) | 20848 | Stat3 |
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| DOID:0090120 | hereditary neutrophilia | MGI:1339755 | Mus musculus (house mouse) | 12986 | Csf3r |
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| DOID:0080052 | acromesomelic dysplasia, Grebe type | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080698 | Teebi hypertelorism syndrome 1 | MGI:1921642 | Mus musculus (house mouse) | 74392 | Specc1l |
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| DOID:0060194 | amyotrophic lateral sclerosis type 2 | MGI:1921268 | Mus musculus (house mouse) | 74018 | Als2 |
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| DOID:0110263 | cataract 19 multiple types | MGI:104698 | Mus musculus (house mouse) | 233187 | Lim2 |
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| DOID:0090018 | autosomal dominant familial periodic fever | MGI:1314884 | Mus musculus (house mouse) | 21937 | Tnfrsf1a |
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| DOID:0050440 | familial partial lipodystrophy | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna |
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| DOID:0110337 | osteogenesis imperfecta type 7 | MGI:1891221 | Mus musculus (house mouse) | 56693 | Crtap |
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| DOID:9352 | type 2 diabetes mellitus | MGI:109334 | Mus musculus (house mouse) | 384783 | Irs2 |
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| DOID:3328 | temporal lobe epilepsy | MGI:95739 | Mus musculus (house mouse) | 14645 | Glul |
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| DOID:0060700 | familial hypocalciuric hypercalcemia 1 | MGI:1351351 | Mus musculus (house mouse) | 12374 | Casr |
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| DOID:0060574 | von Willebrand's disease 2 | MGI:98941 | Mus musculus (house mouse) | 22371 | Vwf |
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| DOID:3633 | beta-mannosidosis | MGI:88175 | Mus musculus (house mouse) | 110173 | Manba |
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| DOID:0080642 | Middle East respiratory syndrome | MGI:94919 | Mus musculus (house mouse) | 13482 | Dpp4 |
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| DOID:0110291 | Leber congenital amaurosis 10 | MGI:2384917 | Mus musculus (house mouse) | 216274 | Cep290 |
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| DOID:14179 | X-linked agammaglobulinemia | MGI:88216 | Mus musculus (house mouse) | 12229 | Btk |
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| DOID:0110350 | osteogenesis imperfecta type 6 | MGI:108080 | Mus musculus (house mouse) | 20317 | Serpinf1 |
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| DOID:0090067 | Fuhrmann syndrome | MGI:98961 | Mus musculus (house mouse) | 22421 | Wnt7a |
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