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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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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:6000 | congestive heart failure | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:1824 | status epilepticus | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:90 | degenerative disc disease | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:4480 | achondroplasia | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:7148 | rheumatoid arthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:0112282 | spondyloepiphyseal dysplasia Kimberley type | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:6000 | congestive heart failure | WB:WBGene00003858 | Caenorhabditis elegans | 176000 | ogt-1 |
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| DOID:9351 | diabetes mellitus | WB:WBGene00003858 | Caenorhabditis elegans | 176000 | ogt-1 |
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| DOID:0080240 | non-syndromic X-linked intellectual disability 106 | WB:WBGene00003858 | Caenorhabditis elegans | 176000 | ogt-1 |
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| DOID:1712 | aortic valve stenosis | WB:WBGene00003858 | Caenorhabditis elegans | 176000 | ogt-1 |
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| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00003858 | Caenorhabditis elegans | 176000 | ogt-1 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | WB:WBGene00015162 | Caenorhabditis elegans | 176032 | algn-11 |
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| DOID:3525 | middle cerebral artery infarction | WB:WBGene00022817 | Caenorhabditis elegans | 176077 | upp-1 |
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| DOID:4079 | heart valve disease | WB:WBGene00001628 | Caenorhabditis elegans | 176112 | gly-3 |
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| DOID:2747 | glycogen storage disease | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0111042 | glycogen storage disease IXa | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0050545 | visceral heterotaxy | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:1459 | hypothyroidism | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:0111040 | glycogen storage disease IXd | WB:WBGene00015754 | Caenorhabditis elegans | 176149 | C14B9.8 |
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| DOID:13359 | Ehlers-Danlos syndrome | WB:WBGene00005021 | Caenorhabditis elegans | 176382 | sqv-3 |
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| DOID:0080738 | Ehlers-Danlos syndrome spondylodysplastic type 1 | WB:WBGene00005021 | Caenorhabditis elegans | 176382 | sqv-3 |
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| DOID:0080554 | congenital disorder of glycosylation Ib | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:2978 | carbohydrate metabolic disorder | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00014013 | Caenorhabditis elegans | 176388 | ZK632.4 |
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| DOID:0110219 | Brugada syndrome 2 | WB:WBGene00010778 | Caenorhabditis elegans | 176399 | gpdh-2 |
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