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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:14679 | VACTERL association | MGI:107736 | Mus musculus (house mouse) | 110350 | Dync2h1 |
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| DOID:0050144 | Kartagener syndrome | MGI:1315205 | Mus musculus (house mouse) | 20563 | Slit2 |
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| DOID:0050545 | visceral heterotaxy | MGI:97515 | Mus musculus (house mouse) | 18552 | Pcsk5 |
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| DOID:0050545 | visceral heterotaxy | MGI:107718 | Mus musculus (house mouse) | 110082 | Dnah5 |
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| DOID:2975 | cystic kidney disease | MGI:2384917 | Mus musculus (house mouse) | 216274 | Cep290 |
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| DOID:0050545 | visceral heterotaxy | MGI:2685906 | Mus musculus (house mouse) | 381738 | Drc1 |
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| DOID:3827 | congenital diaphragmatic hernia | MGI:96828 | Mus musculus (house mouse) | 16971 | Lrp1 |
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| DOID:0050144 | Kartagener syndrome | MGI:2685906 | Mus musculus (house mouse) | 381738 | Drc1 |
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| DOID:0060327 | omphalocele | MGI:96828 | Mus musculus (house mouse) | 16971 | Lrp1 |
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| DOID:2975 | cystic kidney disease | MGI:104757 | Mus musculus (house mouse) | 13846 | Ephb4 |
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| DOID:11984 | hypertrophic cardiomyopathy | MGI:97603 | Mus musculus (house mouse) | 18763 | Pkd1 |
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| DOID:12583 | velocardiofacial syndrome | MGI:1336209 | Mus musculus (house mouse) | 216131 | Trappc10 |
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| DOID:9562 | primary ciliary dyskinesia | MGI:1315205 | Mus musculus (house mouse) | 20563 | Slit2 |
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| DOID:6419 | tetralogy of Fallot | MGI:1338820 | Mus musculus (house mouse) | 12154 | Bmp10 |
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| DOID:11198 | DiGeorge syndrome | MGI:2154244 | Mus musculus (house mouse) | 67784 | Plxnd1 |
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| DOID:2975 | cystic kidney disease | MGI:1315205 | Mus musculus (house mouse) | 20563 | Slit2 |
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| DOID:0050545 | visceral heterotaxy | MGI:1100864 | Mus musculus (house mouse) | 13411 | Dnah11 |
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| DOID:1928 | Williams-Beuren syndrome | MGI:96817 | Mus musculus (house mouse) | 16948 | Lox |
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| DOID:11198 | DiGeorge syndrome | MGI:104719 | Mus musculus (house mouse) | 15531 | Ndst1 |
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| DOID:2975 | cystic kidney disease | MGI:1923928 | Mus musculus (house mouse) | 329795 | Tmem67 |
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| DOID:0050474 | Netherton syndrome | MGI:1919682 | Mus musculus (house mouse) | 72432 | Spink5 |
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| DOID:0090067 | Fuhrmann syndrome | MGI:98961 | Mus musculus (house mouse) | 22421 | Wnt7a |
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| DOID:9970 | obesity | MGI:104663 | Mus musculus (house mouse) | 16846 | Lep |
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| DOID:0050632 | oculocutaneous albinism | MGI:2153040 | Mus musculus (house mouse) | 22293 | Slc45a2 |
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| DOID:480 | movement disease | MGI:109196 | Mus musculus (house mouse) | 13643 | Efnb3 |
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