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GlyTouCan
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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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:1168 | familial hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:0060691 | platelet-type bleeding disorder 16 | MGI:96612 | Mus musculus (house mouse) | 16416 | Itgb3 |
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| DOID:12894 | Sjogren's syndrome | HGNC:11920 | Homo sapiens (human) | 355 | FAS |
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| DOID:9280 | carbamoyl phosphate synthetase I deficiency disease | MGI:891996 | Mus musculus (house mouse) | 227231 | Cps1 |
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| DOID:3328 | temporal lobe epilepsy | HGNC:4583 | Homo sapiens (human) | 2901 | GRIK5 |
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| DOID:0060870 | isolated growth hormone deficiency | RGD:2688 | Rattus norvegicus (Norway rat) | 25321 | Ghrhr |
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| DOID:3652 | Leigh disease | HGNC:11474 | Homo sapiens (human) | 6834 | SURF1 |
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| DOID:0110893 | inflammatory bowel disease 13 | MGI:97570 | Mus musculus (house mouse) | 18671 | Abcb1a |
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| DOID:12930 | dilated cardiomyopathy | HGNC:338 | Homo sapiens (human) | 186 | AGTR2 |
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| DOID:0110870 | congenital stationary night blindness 1A | MGI:2448607 | Mus musculus (house mouse) | 236690 | Nyx |
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| DOID:10632 | Wolfram syndrome | HGNC:12762 | Homo sapiens (human) | 7466 | WFS1 |
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| DOID:10652 | Alzheimer's disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:2377 | multiple sclerosis | MGI:97551 | Mus musculus (house mouse) | 18646 | Prf1 |
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| DOID:2377 | multiple sclerosis | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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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:0060733 | junctional epidermolysis bullosa with pyloric atresia | MGI:96613 | Mus musculus (house mouse) | 192897 | Itgb4 |
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| DOID:10652 | Alzheimer's disease | HGNC:1606 | Homo sapiens (human) | 1234 | CCR5 |
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| DOID:0060855 | autosomal dominant pseudohypoaldosteronism type 1 | HGNC:7979 | Homo sapiens (human) | 4306 | NR3C2 |
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| DOID:5844 | myocardial infarction | RGD:2070 | Rattus norvegicus (Norway rat) | 24180 | Agtr1a |
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| DOID:13141 | uveitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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