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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
LM-GlycoRepo
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:0060041 | autism spectrum disorder | MGI:1096391 | Mus musculus (house mouse) | 18189 | Nrxn1 |
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| DOID:12120 | pulmonary alveolar proteinosis | MGI:1351617 | Mus musculus (house mouse) | 27410 | Abca3 |
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| DOID:0060748 | familial temporal lobe epilepsy 1 | MGI:1861691 | Mus musculus (house mouse) | 56839 | Lgi1 |
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| DOID:0050771 | pheochromocytoma | MGI:97902 | Mus musculus (house mouse) | 19713 | Ret |
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| DOID:8584 | Burkitt lymphoma | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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| DOID:2512 | nevoid basal cell carcinoma syndrome | MGI:105373 | Mus musculus (house mouse) | 19206 | Ptch1 |
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| DOID:0050328 | congenital hypothyroidism | MGI:98813 | Mus musculus (house mouse) | 22018 | Tpo |
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| DOID:0111078 | tibial muscular dystrophy | MGI:98864 | Mus musculus (house mouse) | 22138 | Ttn |
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| DOID:0060835 | isolated microphthalmia 6 | MGI:1916703 | Mus musculus (house mouse) | 69453 | Prss56 |
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| DOID:0110933 | nemaline myopathy 11 | MGI:1916052 | Mus musculus (house mouse) | 68802 | Mypn |
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| DOID:12120 | pulmonary alveolar proteinosis | MGI:1339759 | Mus musculus (house mouse) | 12983 | Csf2rb |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:4184 | pseudohypoparathyroidism | MGI:95777 | Mus musculus (house mouse) | 14683 | Gnas |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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| DOID:14504 | Niemann-Pick disease | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:0080096 | myofibrillar myopathy 5 | MGI:95557 | Mus musculus (house mouse) | 68794 | Flnc |
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| DOID:0110965 | brachydactyly type A2 | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0060041 | autism spectrum disorder | MGI:97441 | Mus musculus (house mouse) | 18390 | Oprm1 |
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| DOID:14705 | Pfeiffer syndrome | MGI:95522 | Mus musculus (house mouse) | 14182 | Fgfr1 |
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| DOID:0050558 | Ullrich congenital muscular dystrophy | MGI:88461 | Mus musculus (house mouse) | 12835 | Col6a3 |
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| DOID:3883 | Lynch syndrome | MGI:101938 | Mus musculus (house mouse) | 17350 | Mlh1 |
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| DOID:10652 | Alzheimer's disease | MGI:97004 | Mus musculus (house mouse) | 17380 | Mme |
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| DOID:12930 | dilated cardiomyopathy | MGI:1914502 | Mus musculus (house mouse) | 67252 | Cap2 |
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| DOID:9744 | type 1 diabetes mellitus | MGI:107474 | Mus musculus (house mouse) | 12494 | Cd38 |
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| DOID:0050144 | Kartagener syndrome | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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