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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:1168 | familial hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:10652 | Alzheimer's disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:783 | end stage renal disease | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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| DOID:0060363 | glycerol kinase deficiency | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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| DOID:1561 | cognitive disorder | MGI:88470 | Mus musculus (house mouse) | 12846 | Comt |
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| DOID:14497 | Wolman disease | MGI:96789 | Mus musculus (house mouse) | 16889 | Lipa |
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| DOID:14692 | Smith-Lemli-Opitz syndrome | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:10763 | hypertension | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:13141 | uveitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:2746 | glycogen storage disease V | HGNC:9726 | Homo sapiens (human) | 5837 | PYGM |
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| DOID:0060639 | permanent neonatal diabetes mellitus | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
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| DOID:9743 | diabetic neuropathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:10609 | rickets | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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| DOID:850 | lung disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4795 | GM2 gangliosidosis, AB variant | MGI:95762 | Mus musculus (house mouse) | 14667 | Gm2a |
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| DOID:2355 | anemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:2747 | glycogen storage disease | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:2747 | glycogen storage disease | RGD:620024 | Rattus norvegicus (Norway rat) | 140671 | Phkg2 |
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| DOID:10652 | Alzheimer's disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050663 | Bethlem myopathy | HGNC:2211 | Homo sapiens (human) | 1291 | COL6A1 |
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| DOID:13088 | periventricular leukomalacia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | MGI:88061 | Mus musculus (house mouse) | 11821 | Aprt |
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| DOID:2750 | glycogen storage disease IV | HGNC:4180 | Homo sapiens (human) | 2632 | GBE1 |
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| DOID:289 | endometriosis | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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