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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:2671 | transitional cell carcinoma | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:11054 | urinary bladder cancer | HGNC:1681 | Homo sapiens (human) | 960 | CD44 |
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| DOID:0080108 | myoglobinuria | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:9970 | obesity | HGNC:14450 | Homo sapiens (human) | 9663 | LPIN2 |
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| DOID:9970 | obesity | HGNC:10660 | Homo sapiens (human) | 9672 | SDC3 |
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| DOID:1485 | cystic fibrosis | HGNC:18967 | Homo sapiens (human) | 9695 | EDEM1 |
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| DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | MGI:2145517 | Mus musculus (house mouse) | 97884 | B3galnt2 |
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| DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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| DOID:10024 | migraine with aura | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:863 | nervous system disease | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:0070384 | developmental and epileptic encephalopathy 98 | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:0060178 | familial hemiplegic migraine | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:14264 | benign neonatal seizures | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:0050635 | alternating hemiplegia of childhood | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:1574 | alcohol use disorder | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:10763 | hypertension | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:1826 | epilepsy | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:0111182 | familial hemiplegic migraine 2 | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:9279 | hyperhomocysteinemia | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:1289 | neurodegenerative disease | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0110184 | Charcot-Marie-Tooth disease type 4J | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0080923 | bilateral parasagittal parieto-occipital polymicrogyria | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0060589 | Yunis-Varon syndrome | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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| DOID:0060202 | amyotrophic lateral sclerosis type 11 | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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