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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
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:0060284 | paroxysmal nocturnal hemoglobinuria | WB:WBGene00008918 | Caenorhabditis elegans | 179519 | pigt-1 |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | WB:WBGene00008918 | Caenorhabditis elegans | 179519 | pigt-1 |
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| DOID:3827 | congenital diaphragmatic hernia | WB:WBGene00008999 | Caenorhabditis elegans | 181229 | myrf-2 |
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| DOID:5614 | eye disease | WB:WBGene00008999 | Caenorhabditis elegans | 181229 | myrf-2 |
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| DOID:0080634 | nanophthalmos | WB:WBGene00008999 | Caenorhabditis elegans | 181229 | myrf-2 |
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| DOID:1405 | primary angle-closure glaucoma | WB:WBGene00008999 | Caenorhabditis elegans | 181229 | myrf-2 |
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| DOID:9834 | hyperopia | WB:WBGene00008999 | Caenorhabditis elegans | 181229 | myrf-2 |
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| DOID:3526 | cerebral infarction | WB:WBGene00008999 | Caenorhabditis elegans | 181229 | myrf-2 |
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| DOID:0070458 | hereditary spastic paraplegia 89 | WB:WBGene00009164 | Caenorhabditis elegans | 172833 | hrdl-1 |
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| DOID:2476 | hereditary spastic paraplegia | WB:WBGene00009164 | Caenorhabditis elegans | 172833 | hrdl-1 |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | WB:WBGene00009192 | Caenorhabditis elegans | 185021 | asah-2 |
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| DOID:0050464 | Farber lipogranulomatosis | WB:WBGene00009192 | Caenorhabditis elegans | 185021 | asah-2 |
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| DOID:1927 | sphingolipidosis | WB:WBGene00009192 | Caenorhabditis elegans | 185021 | asah-2 |
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| DOID:576 | proteinuria | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:8466 | retinal degeneration | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:13603 | obstructive jaundice | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:2527 | nephrosis | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:670 | amphetamine abuse | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:10976 | membranous glomerulonephritis | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:0080301 | atypical hemolytic-uremic syndrome | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:12365 | malaria | WB:WBGene00009500 | Caenorhabditis elegans | 185381 | cfh-1 |
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| DOID:3908 | lung non-small cell carcinoma | WB:WBGene00009717 | Caenorhabditis elegans | 174437 | dep-1 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00009717 | Caenorhabditis elegans | 174437 | dep-1 |
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| DOID:0060108 | brain glioma | WB:WBGene00009717 | Caenorhabditis elegans | 174437 | dep-1 |
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| DOID:3347 | osteosarcoma | WB:WBGene00009717 | Caenorhabditis elegans | 174437 | dep-1 |
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