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GlyTouCan
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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0111266 | geroderma osteodysplasticum | MGI:2138271 | Mus musculus (house mouse) | 98376 | Gorab |
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| DOID:9631 | Pelger-Huet anomaly | MGI:2138281 | Mus musculus (house mouse) | 98386 | Lbr |
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| DOID:9074 | systemic lupus erythematosus | MGI:2138281 | Mus musculus (house mouse) | 98386 | Lbr |
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| DOID:12236 | primary biliary cholangitis | MGI:2138281 | Mus musculus (house mouse) | 98386 | Lbr |
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| DOID:1702 | ichthyosis vulgaris | MGI:2138281 | Mus musculus (house mouse) | 98386 | Lbr |
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| DOID:0111588 | Greenberg dysplasia | MGI:2138281 | Mus musculus (house mouse) | 98386 | Lbr |
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| DOID:13533 | osteopetrosis | HGNC:29017 | Homo sapiens (human) | 9842 | PLEKHM1 |
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| DOID:0110945 | autosomal recessive osteopetrosis 6 | HGNC:29017 | Homo sapiens (human) | 9842 | PLEKHM1 |
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| DOID:1686 | glaucoma | HGNC:4866 | Homo sapiens (human) | 9843 | HEPH |
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| DOID:0080239 | autosomal recessive intellectual developmental disorder 61 | HGNC:23625 | Homo sapiens (human) | 9853 | RUSC2 |
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| DOID:0050816 | urofacial syndrome | HGNC:20889 | Homo sapiens (human) | 9860 | LRIG2 |
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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:9279 | hyperhomocysteinemia | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:10024 | migraine with aura | 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:0070384 | developmental and epileptic encephalopathy 98 | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:0111558 | Charcot-Marie-Tooth disease type 2DD | 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:0060178 | familial hemiplegic migraine | 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:0111182 | familial hemiplegic migraine 2 | MGI:88106 | Mus musculus (house mouse) | 98660 | Atp1a2 |
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| DOID:1324 | lung cancer | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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| DOID:1909 | melanoma | HGNC:10761 | Homo sapiens (human) | 9869 | SETDB1 |
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