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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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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:14115 | toxic shock syndrome | MGI:95394 | Mus musculus (house mouse) | 13807 | Eno2 |
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| DOID:1800 | neuroendocrine carcinoma | MGI:95394 | Mus musculus (house mouse) | 13807 | Eno2 |
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| DOID:12783 | migraine without aura | MGI:95394 | Mus musculus (house mouse) | 13807 | Eno2 |
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| DOID:936 | brain disease | MGI:95394 | Mus musculus (house mouse) | 13807 | Eno2 |
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| DOID:11054 | urinary bladder cancer | MGI:95394 | Mus musculus (house mouse) | 13807 | Eno2 |
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| DOID:10763 | hypertension | MGI:95393 | Mus musculus (house mouse) | 13806 | Eno1 |
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| DOID:10652 | Alzheimer's disease | MGI:95393 | Mus musculus (house mouse) | 13806 | Eno1 |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:0110389 | retinitis pigmentosa 73 | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:0111393 | mucopolysaccharidosis type IIIC | HGNC:26527 | Homo sapiens (human) | 138050 | HGSNAT |
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| DOID:0080000 | muscular disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:936 | brain disease | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:3146 | lipid metabolism disorder | HGNC:2330 | Homo sapiens (human) | 1376 | CPT2 |
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| DOID:0090129 | carnitine palmitoyltransferase I deficiency | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:9970 | obesity | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:12351 | alcoholic hepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:783 | end stage renal disease | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:3146 | lipid metabolism disorder | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:5419 | schizophrenia | HGNC:922 | Homo sapiens (human) | 135152 | B3GAT2 |
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| DOID:9206 | Barrett's esophagus | HGNC:922 | Homo sapiens (human) | 135152 | B3GAT2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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| DOID:0080571 | congenital disorder of glycosylation Iu | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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