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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:0080552 | congenital disorder of glycosylation Ia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:12217 | Lewy body dementia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:3594 | choriocarcinoma | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:635 | acquired immunodeficiency syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:11476 | osteoporosis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:14330 | Parkinson's disease | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:10652 | Alzheimer's disease | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:14681 | Silver-Russell syndrome | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:14183 | alcoholic neuropathy | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0050589 | inflammatory bowel disease | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:4752 | multiple system atrophy | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:77 | gastrointestinal system disease | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:9471 | meningitis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:3454 | brain infarction | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:8577 | ulcerative colitis | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0070403 | hypomyelinating leukodystrophy 26 | HGNC:16872 | Homo sapiens (human) | 347734 | SLC35B2 |
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| DOID:1485 | cystic fibrosis | FB:FBgn0032480 | Drosophila melanogaster (fruit fly) | 34714 | Edem2 | CG5682 |
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| DOID:0050571 | congenital disorder of glycosylation type II | FB:FBgn0032480 | Drosophila melanogaster (fruit fly) | 34714 | Edem2 | CG5682 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | FB:FBgn0032477 | Drosophila melanogaster (fruit fly) | 34711 | Alg7 | CG5287 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | FB:FBgn0032477 | Drosophila melanogaster (fruit fly) | 34711 | Alg7 | CG5287 |
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| DOID:10652 | Alzheimer's disease | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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