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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:1059 | intellectual disability | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:0050771 | pheochromocytoma | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:10763 | hypertension | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:2986 | IgA glomerulonephritis | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:783 | end stage renal disease | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:10283 | prostate cancer | HGNC:1929 | Homo sapiens (human) | 1113 | CHGA |
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| DOID:1682 | congenital heart disease | HGNC:12757 | Homo sapiens (human) | 11091 | WDR5 |
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| DOID:0111773 | 46,XY sex reversal 8 | HGNC:387 | Homo sapiens (human) | 1109 | AKR1C4 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:10652 | Alzheimer's disease | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:1596 | depressive disorder | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:2841 | asthma | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:3633 | beta-mannosidosis | MGI:88175 | Mus musculus (house mouse) | 110173 | Manba |
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| DOID:2978 | carbohydrate metabolic disorder | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:0080554 | congenital disorder of glycosylation Ib | MGI:97075 | Mus musculus (house mouse) | 110119 | Mpi |
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| DOID:3650 | lactic acidosis | MGI:97829 | Mus musculus (house mouse) | 110095 | Pygl |
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| DOID:2754 | glycogen storage disease VI | MGI:97829 | Mus musculus (house mouse) | 110095 | Pygl |
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| DOID:2747 | glycogen storage disease | MGI:97829 | Mus musculus (house mouse) | 110095 | Pygl |
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| DOID:0111042 | glycogen storage disease IXa | MGI:97577 | Mus musculus (house mouse) | 110094 | Phka2 |
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