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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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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:1793 | pancreatic cancer | RGD:2289 | Rattus norvegicus (Norway rat) | 24889 | Cckar |
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| DOID:8584 | Burkitt lymphoma | HGNC:7553 | Homo sapiens (human) | 4609 | MYC |
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| DOID:10652 | Alzheimer's disease | MGI:97180 | Mus musculus (house mouse) | 17762 | Mapt |
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| DOID:12120 | pulmonary alveolar proteinosis | MGI:1339752 | Mus musculus (house mouse) | 12981 | Csf2 |
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| DOID:1929 | supravalvular aortic stenosis | HGNC:3327 | Homo sapiens (human) | 2006 | ELN |
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| DOID:10763 | hypertension | RGD:628678 | Rattus norvegicus (Norway rat) | 260320 | F7 |
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| DOID:0110910 | leukocyte adhesion deficiency 1 | MGI:96611 | Mus musculus (house mouse) | 16414 | Itgb2 |
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| DOID:3770 | pulmonary fibrosis | HGNC:3176 | Homo sapiens (human) | 1906 | EDN1 |
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| DOID:2921 | glomerulonephritis | RGD:628868 | Rattus norvegicus (Norway rat) | 29302 | Itgb3 |
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| DOID:9266 | cystinuria | HGNC:11025 | Homo sapiens (human) | 6519 | SLC3A1 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:61 | Homo sapiens (human) | 215 | ABCD1 |
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| DOID:10487 | Hirschsprung's disease | HGNC:3180 | Homo sapiens (human) | 1910 | EDNRB |
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| DOID:10983 | Alport syndrome | HGNC:2204 | Homo sapiens (human) | 1285 | COL4A3 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:99454 | Mus musculus (house mouse) | 16367 | Irs1 |
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| DOID:3320 | Tay-Sachs disease | MGI:96073 | Mus musculus (house mouse) | 15211 | Hexa |
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| DOID:0060246 | MASA syndrome | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:10908 | hydrocephalus | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1859214 | Mus musculus (house mouse) | 54128 | Pmm2 |
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| DOID:3042 | allergic contact dermatitis | RGD:619991 | Rattus norvegicus (Norway rat) | 83785 | Vegfa |
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| DOID:3042 | allergic contact dermatitis | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:0111040 | glycogen storage disease IXd | MGI:97576 | Mus musculus (house mouse) | 18679 | Phka1 |
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| DOID:0080026 | otospondylomegaepiphyseal dysplasia, autosomal recessive | HGNC:2187 | Homo sapiens (human) | 1302 | COL11A2 |
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| DOID:14452 | hypokalemic periodic paralysis | HGNC:1397 | Homo sapiens (human) | 779 | CACNA1S |
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| DOID:9452 | steatotic liver disease | HGNC:4801 | Homo sapiens (human) | 3030 | HADHA |
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| DOID:9883 | Becker muscular dystrophy | MGI:94909 | Mus musculus (house mouse) | 13405 | Dmd |
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