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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9282 | ocular hypertension | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:14679 | VACTERL association | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:2986 | IgA glomerulonephritis | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:0060041 | autism spectrum disorder | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:0110875 | holoprosencephaly 3 | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:9253 | gastrointestinal stromal tumor | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:1148 | polydactyly | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:784 | chronic kidney disease | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:0111564 | hypoplastic or aplastic tibia with polydactyly | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:10487 | Hirschsprung's disease | WB:WBGene00006952 | Caenorhabditis elegans | 180638 | wrt-6 |
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| DOID:0080442 | developmental and epileptic encephalopathy 41 | WB:WBGene00001620 | Caenorhabditis elegans | 180641 | glt-1 |
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| DOID:12858 | Huntington's disease | WB:WBGene00001620 | Caenorhabditis elegans | 180641 | glt-1 |
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| DOID:3525 | middle cerebral artery infarction | WB:WBGene00001620 | Caenorhabditis elegans | 180641 | glt-1 |
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| DOID:332 | amyotrophic lateral sclerosis | WB:WBGene00001620 | Caenorhabditis elegans | 180641 | glt-1 |
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| DOID:0050579 | glycogen storage disease XV | WB:WBGene00006863 | Caenorhabditis elegans | 180644 | gyg-1 |
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| DOID:1059 | intellectual disability | WB:WBGene00003007 | Caenorhabditis elegans | 180679 | lin-18 |
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| DOID:9970 | obesity | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:0060040 | pervasive developmental disorder | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:3227 | tracheal stenosis | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:783 | end stage renal disease | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:529 | blepharospasm | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:12858 | Huntington's disease | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:4195 | hyperglycemia | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:1094 | attention deficit hyperactivity disorder | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
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| DOID:1596 | depressive disorder | WB:WBGene00001052 | Caenorhabditis elegans | 180714 | dop-1 |
|
