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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:2747 | glycogen storage disease | WB:WBGene00001793 | Caenorhabditis elegans | 174924 | gsy-1 |
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| DOID:3534 | Lafora disease | WB:WBGene00001793 | Caenorhabditis elegans | 174924 | gsy-1 |
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| DOID:3211 | lysosomal storage disease | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:0050461 | aspartylglucosaminuria | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:5212 | congenital disorder of glycosylation | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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| DOID:0080556 | congenital disorder of glycosylation Id | WB:WBGene00010720 | Caenorhabditis elegans | 175065 | algn-3 |
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| DOID:332 | amyotrophic lateral sclerosis | WB:WBGene00006575 | Caenorhabditis elegans | 175502 | tir-1 |
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| DOID:1289 | neurodegenerative disease | WB:WBGene00006575 | Caenorhabditis elegans | 175502 | tir-1 |
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| DOID:0111459 | classic galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:9870 | galactosemia | WB:WBGene00014203 | Caenorhabditis elegans | 175506 | ZK1058.3 |
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| DOID:9744 | type 1 diabetes mellitus | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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| DOID:3803 | Crigler-Najjar syndrome | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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| DOID:2741 | bilirubin metabolic disorder | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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| DOID:7998 | hyperthyroidism | WB:WBGene00010904 | Caenorhabditis elegans | 175591 | ugt-62 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00017166 | Caenorhabditis elegans | 175827 | aldo-2 |
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| DOID:5154 | borna disease | WB:WBGene00017166 | Caenorhabditis elegans | 175827 | aldo-2 |
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| DOID:438 | autoimmune disease of the nervous system | WB:WBGene00017166 | Caenorhabditis elegans | 175827 | aldo-2 |
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| DOID:0080573 | congenital disorder of glycosylation Ix | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | WB:WBGene00020437 | Caenorhabditis elegans | 175886 | stt-3 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:5212 | congenital disorder of glycosylation | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | WB:WBGene00020820 | Caenorhabditis elegans | 175920 | algn-1 |
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| DOID:8398 | osteoarthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:2377 | multiple sclerosis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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