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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:0110078 | Leber congenital amaurosis 1 | MGI:105123 | Mus musculus (house mouse) | 14919 | Gucy2e |
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| DOID:14365 | systemic primary carnitine deficiency disease | MGI:1329012 | Mus musculus (house mouse) | 20520 | Slc22a5 |
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| DOID:0050473 | Alstrom syndrome | MGI:1934606 | Mus musculus (house mouse) | 236266 | Alms1 |
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| DOID:0110011 | advanced sleep phase syndrome 1 | MGI:1195265 | Mus musculus (house mouse) | 18627 | Per2 |
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| DOID:9970 | obesity | MGI:101932 | Mus musculus (house mouse) | 12876 | Cpe |
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| DOID:11836 | clubfoot | MGI:1921303 | Mus musculus (house mouse) | 74053 | Grip1 |
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| DOID:1838 | Menkes disease | MGI:99400 | Mus musculus (house mouse) | 11977 | Atp7a |
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| DOID:0060696 | hyperekplexia 1 | MGI:95747 | Mus musculus (house mouse) | 14654 | Glra1 |
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| DOID:0110725 | neuronal ceroid lipofuscinosis 10 | MGI:88562 | Mus musculus (house mouse) | 13033 | Ctsd |
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| DOID:0060757 | sclerosteosis 2 | MGI:2442252 | Mus musculus (house mouse) | 228357 | Lrp4 |
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| DOID:0060832 | Griscelli syndrome type 1 | MGI:105976 | Mus musculus (house mouse) | 17918 | Myo5a |
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| DOID:0050632 | oculocutaneous albinism | MGI:97454 | Mus musculus (house mouse) | 18431 | Oca2 |
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| DOID:0110376 | retinitis pigmentosa 41 | MGI:1100886 | Mus musculus (house mouse) | 19126 | Prom1 |
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| DOID:0050328 | congenital hypothyroidism | MGI:98849 | Mus musculus (house mouse) | 22095 | Tshr |
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| DOID:0050540 | Charcot-Marie-Tooth disease type 3 | MGI:97631 | Mus musculus (house mouse) | 18858 | Pmp22 |
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| DOID:0110153 | Charcot-Marie-Tooth disease type 1E | MGI:97631 | Mus musculus (house mouse) | 18858 | Pmp22 |
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| DOID:0060843 | hereditary neuropathy with liability to pressure palsies | MGI:97631 | Mus musculus (house mouse) | 18858 | Pmp22 |
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| DOID:0110148 | Charcot-Marie-Tooth disease type 1A | MGI:97631 | Mus musculus (house mouse) | 18858 | Pmp22 |
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| DOID:0110726 | neuronal ceroid lipofuscinosis 2 | MGI:1336194 | Mus musculus (house mouse) | 12751 | Tpp1 |
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| DOID:0050794 | multiple synostoses syndrome | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0050790 | fibular hypoplasia and complex brachydactyly | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0110970 | brachydactyly type C | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080052 | acromesomelic dysplasia, Grebe type | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0080051 | acromesomelic dysplasia, Hunter-Thompson type | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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| DOID:0110977 | brachydactyly type A1C | MGI:95688 | Mus musculus (house mouse) | 14563 | Gdf5 |
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