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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:0110371 | retinitis pigmentosa 56 | MGI:3044955 | Mus musculus (house mouse) | 224224 | Impg2 |
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| DOID:0060614 | ulnar-mammary syndrome | MGI:98495 | Mus musculus (house mouse) | 21386 | Tbx3 |
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| DOID:0050144 | Kartagener syndrome | MGI:1916172 | Mus musculus (house mouse) | 68922 | Dnai1 |
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| DOID:3827 | congenital diaphragmatic hernia | MGI:2670972 | Mus musculus (house mouse) | 329872 | Frem1 |
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| DOID:0111129 | focal segmental glomerulosclerosis 2 | MGI:109523 | Mus musculus (house mouse) | 22068 | Trpc6 |
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| DOID:4249 | Gerstmann-Straussler-Scheinker syndrome | MGI:97769 | Mus musculus (house mouse) | 19122 | Prnp |
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| DOID:0050778 | Meckel syndrome | MGI:1923928 | Mus musculus (house mouse) | 329795 | Tmem67 |
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| DOID:0060691 | platelet-type bleeding disorder 16 | MGI:96601 | Mus musculus (house mouse) | 16399 | Itga2b |
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| DOID:2746 | glycogen storage disease V | MGI:97830 | Mus musculus (house mouse) | 19309 | Pygm |
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| DOID:0112276 | neurodevelopmental disorder with involuntary movements | MGI:95775 | Mus musculus (house mouse) | 14681 | Gnao1 |
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| DOID:206 | hereditary multiple exostoses | MGI:108050 | Mus musculus (house mouse) | 14043 | Ext2 |
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| DOID:12801 | mucopolysaccharidosis III | MGI:1922862 | Mus musculus (house mouse) | 75612 | Gns |
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| DOID:5419 | schizophrenia | MGI:99779 | Mus musculus (house mouse) | 11441 | Chrna7 |
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| DOID:10825 | essential hypertension | MGI:97362 | Mus musculus (house mouse) | 18127 | Nos3 |
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| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | MGI:107537 | Mus musculus (house mouse) | 12752 | Cln3 |
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| DOID:0060695 | hyperekplexia | MGI:95747 | Mus musculus (house mouse) | 14654 | Glra1 |
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| DOID:0110859 | polycystic kidney disease 2 | MGI:1099818 | Mus musculus (house mouse) | 18764 | Pkd2 |
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| DOID:0060041 | autism spectrum disorder | MGI:2179435 | Mus musculus (house mouse) | 192167 | Nlgn1 |
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| DOID:0060234 | Carpenter syndrome | MGI:2446294 | Mus musculus (house mouse) | 269878 | Megf8 |
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| DOID:12388 | neurohypophyseal diabetes insipidus | MGI:88121 | Mus musculus (house mouse) | 11998 | Avp |
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| DOID:0111814 | methylmalonic acidemia and homocysteinemia cblX type | MGI:105942 | Mus musculus (house mouse) | 15161 | Hcfc1 |
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| DOID:0090017 | epidermolysis bullosa simplex with muscular dystrophy | MGI:1277961 | Mus musculus (house mouse) | 18810 | Plec |
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| DOID:0110939 | autosomal recessive osteopetrosis 5 | MGI:2655574 | Mus musculus (house mouse) | 14628 | Ostm1 |
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| DOID:0110199 | Charcot-Marie-Tooth disease dominant intermediate C | MGI:2147627 | Mus musculus (house mouse) | 107271 | Yars1 |
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| DOID:14330 | Parkinson's disease | MGI:1342774 | Mus musculus (house mouse) | 19017 | Ppargc1a |
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