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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:3908 | lung non-small cell carcinoma | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:219 | colon cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:1793 | pancreatic cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:1324 | lung cancer | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4242 | Homo sapiens (human) | 9945 | GFPT2 |
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| DOID:1440 | Machado-Joseph disease | HGNC:4242 | Homo sapiens (human) | 9945 | GFPT2 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0050453 | lissencephaly | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0111237 | congenital muscular dystrophy-dystroglycanopathy type A1 | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:9884 | muscular dystrophy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0110297 | autosomal recessive limb-girdle muscular dystrophy type 2K | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:0050700 | cardiomyopathy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:9296 | cleft lip | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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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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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:16873 | Homo sapiens (human) | 9896 | FIG4 |
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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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