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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: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:1838 | Menkes disease | HGNC:6664 | Homo sapiens (human) | 4015 | LOX |
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| DOID:2750 | glycogen storage disease IV | HGNC:4180 | Homo sapiens (human) | 2632 | GBE1 |
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| DOID:12308 | Dubin-Johnson syndrome | RGD:2366 | Rattus norvegicus (Norway rat) | 25303 | Abcc2 |
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| DOID:3209 | junctional epidermolysis bullosa | HGNC:6483 | Homo sapiens (human) | 3909 | LAMA3 |
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| DOID:11394 | adult respiratory distress syndrome | RGD:3747 | Rattus norvegicus (Norway rat) | 24795 | Serpina3n |
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| DOID:10763 | hypertension | HGNC:6664 | Homo sapiens (human) | 4015 | LOX |
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| DOID:289 | endometriosis | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:0110666 | congenital myasthenic syndrome 3A | MGI:87893 | Mus musculus (house mouse) | 11447 | Chrnd |
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| DOID:10652 | Alzheimer's disease | HGNC:15917 | Homo sapiens (human) | 23236 | PLCB1 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0060870 | isolated growth hormone deficiency | HGNC:4266 | Homo sapiens (human) | 2692 | GHRHR |
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| DOID:0050470 | Donohue syndrome | MGI:96575 | Mus musculus (house mouse) | 16337 | Insr |
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| DOID:9280 | carbamoyl phosphate synthetase I deficiency disease | HGNC:2323 | Homo sapiens (human) | 1373 | CPS1 |
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| DOID:2750 | glycogen storage disease IV | SGD:S000000737 | Saccharomyces cerevisiae S288C | 856705 | GLC3 |
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| DOID:0110339 | osteogenesis imperfecta type 3 | MGI:88468 | Mus musculus (house mouse) | 12843 | Col1a2 |
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| DOID:9252 | amino acid metabolic disorder | HGNC:5005 | Homo sapiens (human) | 3155 | HMGCL |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | MGI:95797 | Mus musculus (house mouse) | 14751 | Gpi1 |
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| DOID:14761 | Greig cephalopolysyndactyly syndrome | MGI:95729 | Mus musculus (house mouse) | 14634 | Gli3 |
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| DOID:3310 | atopic dermatitis | HGNC:6014 | Homo sapiens (human) | 3565 | IL4 |
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| DOID:10763 | hypertension | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0050427 | xeroderma pigmentosum | HGNC:12816 | Homo sapiens (human) | 7508 | XPC |
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| DOID:11394 | adult respiratory distress syndrome | HGNC:3176 | Homo sapiens (human) | 1906 | EDN1 |
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| DOID:2841 | asthma | HGNC:11526 | Homo sapiens (human) | 6869 | TACR1 |
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