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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:0060180 | colitis | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:3407 | carotid artery disease | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:3498 | pancreatic ductal adenocarcinoma | HGNC:12705 | Homo sapiens (human) | 8876 | VNN1 |
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| DOID:1682 | congenital heart disease | HGNC:12757 | Homo sapiens (human) | 11091 | WDR5 |
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| DOID:0080941 | acquired angioedema | HGNC:12823 | Homo sapiens (human) | 7512 | XPNPEP2 |
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| DOID:1574 | alcohol use disorder | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:10652 | Alzheimer's disease | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:14330 | Parkinson's disease | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:3146 | lipid metabolism disorder | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:811 | lipodystrophy | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:0080108 | myoglobinuria | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:11981 | morbid obesity | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:9970 | obesity | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:783 | end stage renal disease | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:0060292 | X-linked chondrodysplasia punctata 1 | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:12305 | Bloch-Sulzberger syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:162 | cancer | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:0050645 | arterial tortuosity syndrome | HGNC:13444 | Homo sapiens (human) | 81031 | SLC2A10 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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| DOID:0111239 | congenital muscular dystrophy-dystroglycanopathy type A10 | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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| DOID:11714 | gestational diabetes | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:3393 | coronary artery disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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