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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:13809 | familial combined hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:5844 | myocardial infarction | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:10652 | Alzheimer's disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:14221 | abdominal obesity-metabolic syndrome 1 | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:0080000 | muscular disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:10763 | hypertension | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:14118 | familial lipoprotein lipase deficiency | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:1168 | familial hyperlipidemia | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:783 | end stage renal disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:3393 | coronary artery disease | HGNC:6677 | Homo sapiens (human) | 4023 | LPL |
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| DOID:9719 | neovascular inflammatory vitreoretinopathy | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:10629 | microphthalmia | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0050770 | polycystic liver disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:971 | tendinitis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:12559 | idiopathic juvenile osteoporosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0111411 | exudative vitreoretinopathy 4 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0050535 | exudative vitreoretinopathy | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:4079 | heart valve disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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