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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:10591 | pre-eclampsia | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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| DOID:0060256 | Dowling-Degos disease | WB:WBGene00015793 | Caenorhabditis elegans | 180607 | pfut-1 |
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| DOID:1826 | epilepsy | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:9970 | obesity | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:3525 | middle cerebral artery infarction | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:0050866 | oral squamous cell carcinoma | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:0050827 | rheumatic heart disease | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:0060108 | brain glioma | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:8947 | diabetic retinopathy | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:3319 | lymphangioleiomyomatosis | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:2747 | glycogen storage disease | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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| DOID:11721 | glycogen storage disease VII | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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| DOID:0014667 | disease of metabolism | WB:WBGene00022199 | Caenorhabditis elegans | 180583 | pfk-1.1 |
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| DOID:3211 | lysosomal storage disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3323 | Sandhoff disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3320 | Tay-Sachs disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:12377 | spinal muscular atrophy | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | WB:WBGene00001629 | Caenorhabditis elegans | 180302 | gly-4 |
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| DOID:0050579 | glycogen storage disease XV | WB:WBGene00012020 | Caenorhabditis elegans | 180119 | gyg-2 |
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| DOID:2747 | glycogen storage disease | WB:WBGene00012020 | Caenorhabditis elegans | 180119 | gyg-2 |
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| DOID:0080488 | mucolipidosis | MGI:97305 | Mus musculus (house mouse) | 18010 | Neu1 |
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| DOID:3343 | glycoproteinosis | MGI:97305 | Mus musculus (house mouse) | 18010 | Neu1 |
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| DOID:687 | hepatoblastoma | HGNC:3002 | Homo sapiens (human) | 1800 | DPEP1 |
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| DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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