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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▲ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:684 | hepatocellular carcinoma | MGI:2384588 | Mus musculus (house mouse) | 234258 | Neil3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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| DOID:5212 | congenital disorder of glycosylation | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | MGI:2384774 | Mus musculus (house mouse) | 208211 | Alg1 |
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| DOID:0080537 | hypermanganesemia with dystonia 2 | MGI:2384851 | Mus musculus (house mouse) | 213053 | Slc39a14 |
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| DOID:4194 | glucose metabolism disease | MGI:2384910 | Mus musculus (house mouse) | 216019 | Hkdc1 |
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| DOID:10584 | retinitis pigmentosa | MGI:2384910 | Mus musculus (house mouse) | 216019 | Hkdc1 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | MGI:2384919 | Mus musculus (house mouse) | 216395 | Rxylt1 |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:2384919 | Mus musculus (house mouse) | 216395 | Rxylt1 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | MGI:2384966 | Mus musculus (house mouse) | 217664 | Mgat2 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | MGI:2384987 | Mus musculus (house mouse) | 218271 | B4galt7 |
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| DOID:13359 | Ehlers-Danlos syndrome | MGI:2384987 | Mus musculus (house mouse) | 218271 | B4galt7 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:2385025 | Mus musculus (house mouse) | 223774 | Alg12 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | MGI:2385025 | Mus musculus (house mouse) | 223774 | Alg12 |
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| DOID:2747 | glycogen storage disease | MGI:2385254 | Mus musculus (house mouse) | 232493 | Gys2 |
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| DOID:3534 | Lafora disease | MGI:2385254 | Mus musculus (house mouse) | 232493 | Gys2 |
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| DOID:3650 | lactic acidosis | MGI:2385311 | Mus musculus (house mouse) | 235339 | Dlat |
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| DOID:3649 | pyruvate decarboxylase deficiency | MGI:2385311 | Mus musculus (house mouse) | 235339 | Dlat |
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| DOID:4450 | renal cell carcinoma | MGI:2387203 | Mus musculus (house mouse) | 231327 | Ppat |
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| DOID:684 | hepatocellular carcinoma | MGI:2387203 | Mus musculus (house mouse) | 231327 | Ppat |
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| DOID:5419 | schizophrenia | MGI:2389490 | Mus musculus (house mouse) | 280645 | B3gat2 |
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| DOID:9206 | Barrett's esophagus | MGI:2389490 | Mus musculus (house mouse) | 280645 | B3gat2 |
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| DOID:0110728 | neuronal ceroid lipofuscinosis 5 | MGI:2442253 | Mus musculus (house mouse) | 211286 | Cln5 |
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| DOID:1094 | attention deficit hyperactivity disorder | MGI:2442406 | Mus musculus (house mouse) | 338362 | Ust |
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| DOID:9870 | galactosemia | MGI:2442420 | Mus musculus (house mouse) | 319625 | Galm |
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