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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:557 | kidney disease | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:9281 | phenylketonuria | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:2355 | anemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:583 | hemolytic anemia | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:9744 | type 1 diabetes mellitus | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:6713 | cerebrovascular disease | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:9970 | obesity | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:13413 | hepatic encephalopathy | WB:WBGene00007108 | Caenorhabditis elegans | 178046 | gspd-1 |
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| DOID:2748 | glycogen storage disease III | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:4676 | uremia | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | WB:WBGene00008775 | Caenorhabditis elegans | 177998 | mogs-1 |
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| DOID:5154 | borna disease | WB:WBGene00004051 | Caenorhabditis elegans | 177683 | parg-1 |
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| DOID:3454 | brain infarction | WB:WBGene00004051 | Caenorhabditis elegans | 177683 | parg-1 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | WB:WBGene00004051 | Caenorhabditis elegans | 177683 | parg-1 |
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| DOID:3827 | congenital diaphragmatic hernia | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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| DOID:0081210 | autosomal recessive intellectual developmental disorder 46 | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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| DOID:1059 | intellectual disability | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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| DOID:12716 | newborn respiratory distress syndrome | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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| DOID:0060041 | autism spectrum disorder | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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| DOID:11198 | DiGeorge syndrome | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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| DOID:14227 | azoospermia | WB:WBGene00002028 | Caenorhabditis elegans | 177675 | hst-1 |
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| DOID:2018 | hyperinsulinism | WB:WBGene00019295 | Caenorhabditis elegans | 177363 | pfkb-1.2 |
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| DOID:0110960 | Gaucher's disease perinatal lethal | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:0112250 | Gaucher's disease type IIIC | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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