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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▼ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:9352 | type 2 diabetes mellitus | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:14330 | Parkinson's disease | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:0111438 | optic atrophy 5 | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:784 | chronic kidney disease | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:0070347 | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:13711 | dental fluorosis | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:10652 | Alzheimer's disease | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:0060304 | dyschromatosis universalis hereditaria | HGNC:47 | Homo sapiens (human) | 10058 | ABCB6 |
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| DOID:1793 | pancreatic cancer | HGNC:56 | Homo sapiens (human) | 10057 | ABCC5 |
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| DOID:4231 | histiocytoma | HGNC:48357 | Homo sapiens (human) | 100528032 | KLRC4-KLRK1 |
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| DOID:8947 | diabetic retinopathy | HGNC:8104 | Homo sapiens (human) | 100506658 | OCLN |
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| DOID:8778 | Crohn's disease | HGNC:8104 | Homo sapiens (human) | 100506658 | OCLN |
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| DOID:0050656 | pseudo-TORCH syndrome 1 | HGNC:8104 | Homo sapiens (human) | 100506658 | OCLN |
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| DOID:10591 | pre-eclampsia | HGNC:48925 | Homo sapiens (human) | 100506013 | APELA |
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| DOID:526 | human immunodeficiency virus infectious disease | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:14115 | toxic shock syndrome | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:2841 | asthma | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:3312 | bipolar disorder | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:2377 | multiple sclerosis | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:2945 | severe acute respiratory syndrome | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:14330 | Parkinson's disease | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:0060892 | late onset Parkinson's disease | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:7188 | autoimmune thyroiditis | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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| DOID:1205 | allergic disease | MGI:95900 | Mus musculus (house mouse) | 100504404 | H2-Ea |
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