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GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
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:9884 | muscular dystrophy | WB:WBGene00020128 | Caenorhabditis elegans | 182256 | R193.2 |
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| DOID:10825 | essential hypertension | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:0070316 | Miura type epiphyseal chondrodysplasia | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:0080050 | acromesomelic dysplasia, Maroteaux type | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:0080006 | bone development disease | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:5844 | myocardial infarction | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:4480 | achondroplasia | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:10763 | hypertension | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:0111933 | phosphoglycerate kinase 1 deficiency | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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| DOID:14330 | Parkinson's disease | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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| DOID:583 | hemolytic anemia | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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| DOID:162 | cancer | WB:WBGene00020185 | Caenorhabditis elegans | 171965 | pgk-1 |
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| DOID:0081097 | Rafiq syndrome | WB:WBGene00020197 | Caenorhabditis elegans | 180787 | mans-3 |
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| DOID:1508 | candidiasis | WB:WBGene00020222 | Caenorhabditis elegans | 188084 | fut-6 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:10763 | hypertension | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:824 | periodontitis | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:9246 | cerebral amyloid angiopathy | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:6000 | congestive heart failure | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:0110160 | Charcot-Marie-Tooth disease axonal type 2T | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:0050445 | X-linked dominant hypophosphatemic rickets | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:0111745 | cerebellar ataxia type 43 | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:10273 | heart conduction disease | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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| DOID:10754 | otitis media | WB:WBGene00020230 | Caenorhabditis elegans | 188090 | nep-2 |
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