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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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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:10223 | dermatomyositis | HGNC:11086 | Homo sapiens (human) | 9353 | SLIT2 |
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| DOID:0081023 | retinal cone dystrophy 4 | HGNC:20202 | Homo sapiens (human) | 93589 | CACNA2D4 |
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| DOID:2316 | brain ischemia | HGNC:9479 | Homo sapiens (human) | 9361 | LONP1 |
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| DOID:326 | ischemia | HGNC:9479 | Homo sapiens (human) | 9361 | LONP1 |
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| DOID:0111274 | CODAS syndrome | HGNC:9479 | Homo sapiens (human) | 9361 | LONP1 |
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| DOID:1074 | kidney failure | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:784 | chronic kidney disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:0111063 | hyperphosphatemic familial tumoral calcinosis | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:4372 | intracranial embolism | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:10584 | retinitis pigmentosa | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:1168 | familial hyperlipidemia | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:557 | kidney disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:10763 | hypertension | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:783 | end stage renal disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:9675 | pulmonary emphysema | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:12466 | secondary hyperparathyroidism | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:2247 | spondylosis | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:3393 | coronary artery disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:0080953 | amelogenesis imperfecta type 1J | HGNC:14376 | Homo sapiens (human) | 93650 | ACP4 |
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| DOID:12336 | male infertility | HGNC:24205 | Homo sapiens (human) | 93661 | CAPZA3 |
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| DOID:0111021 | cone-rod dystrophy 15 | RGD:620420 | Rattus norvegicus (Norway rat) | 93662 | Cdhr1 |
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| DOID:9146 | visceral leishmaniasis | MGI:2135946 | Mus musculus (house mouse) | 93671 | Cd163 |
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| DOID:936 | brain disease | MGI:2135946 | Mus musculus (house mouse) | 93671 | Cd163 |
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| DOID:8476 | Whipple disease | MGI:2135946 | Mus musculus (house mouse) | 93671 | Cd163 |
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