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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:0111680 | essential fructosuria | HGNC:6315 | Homo sapiens (human) | 3795 | KHK |
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| DOID:0111680 | essential fructosuria | RGD:2966 | Rattus norvegicus (Norway rat) | 25659 | Khk |
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| DOID:0111677 | familial benign fleck retina | HGNC:9038 | Homo sapiens (human) | 5322 | PLA2G5 |
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| DOID:0111673 | Saul-Wilson syndrome | HGNC:18620 | Homo sapiens (human) | 25839 | COG4 |
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| DOID:0111673 | Saul-Wilson syndrome | SGD:S000006309 | Saccharomyces cerevisiae S288C | 856220 | COG4 |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0111671 | primary hyperoxaluria type 2 | HGNC:4570 | Homo sapiens (human) | 9380 | GRHPR |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:0111646 | congenital lactase deficiency | HGNC:6530 | Homo sapiens (human) | 3938 | LCT |
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| DOID:0111633 | congenital sucrase-isomaltase deficiency | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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| DOID:0111630 | familial erythrocytosis 8 | SGD:S000001635 | Saccharomyces cerevisiae S288C | 853705 | GPM1 |
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| DOID:0111630 | familial erythrocytosis 8 | HGNC:1093 | Homo sapiens (human) | 669 | BPGM |
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| DOID:0111630 | familial erythrocytosis 8 | MGI:1098242 | Mus musculus (house mouse) | 12183 | Bpgm |
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| DOID:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
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| DOID:0111626 | D-glyceric aciduria | RGD:1591498 | Rattus norvegicus (Norway rat) | 684314 | Glyctk |
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| DOID:0111626 | D-glyceric aciduria | MGI:2444085 | Mus musculus (house mouse) | 235582 | Glyctk |
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| DOID:0111619 | combined D-2- and L-2-hydroxyglutaric aciduria | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0111582 | hereditary arterial and articular multiple calcification syndrome | HGNC:8021 | Homo sapiens (human) | 4907 | NT5E |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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| DOID:0111503 | Li-Fraumeni syndrome 1 | RGD:3889 | Rattus norvegicus (Norway rat) | 24842 | Tp53 |
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| DOID:0111503 | Li-Fraumeni syndrome 1 | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0111503 | Li-Fraumeni syndrome 1 | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:0111460 | cardiofaciocutaneous syndrome 1 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0111460 | cardiofaciocutaneous syndrome 1 | MGI:88190 | Mus musculus (house mouse) | 109880 | Braf |
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