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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
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:10652 | Alzheimer's disease | RGD:620970 | Rattus norvegicus (Norway rat) | 84599 | Tmed10 |
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| DOID:1936 | atherosclerosis | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:12466 | secondary hyperparathyroidism | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:5844 | myocardial infarction | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:13543 | hyperparathyroidism | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:12678 | hypercalcemia | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0050700 | cardiomyopathy | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0111322 | idiopathic generalized epilepsy 8 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0090107 | autosomal dominant hypocalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0060700 | familial hypocalciuric hypercalcemia 1 | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:6432 | pulmonary hypertension | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:783 | end stage renal disease | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:585 | nephrolithiasis | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:1059 | intellectual disability | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0080652 | calcium oxalate nephrolithiasis | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0090109 | autosomal dominant hypocalcemia | HGNC:1514 | Homo sapiens (human) | 846 | CASR |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:12020 | Homo sapiens (human) | 8460 | TPST1 |
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| DOID:891 | progressive myoclonus epilepsy | RGD:69278 | Rattus norvegicus (Norway rat) | 84609 | Sema6b |
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| DOID:0090132 | complex cortical dysplasia with other brain malformations 7 | HGNC:20776 | Homo sapiens (human) | 84617 | TUBB6 |
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| DOID:0050997 | cerebellar ataxia, mental retardation and dysequlibrium syndrome | HGNC:20776 | Homo sapiens (human) | 84617 | TUBB6 |
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| DOID:0060260 | ptosis | HGNC:20776 | Homo sapiens (human) | 84617 | TUBB6 |
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| DOID:13934 | facial paralysis | HGNC:20776 | Homo sapiens (human) | 84617 | TUBB6 |
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| DOID:0112227 | tubulinopathy | HGNC:20776 | Homo sapiens (human) | 84617 | TUBB6 |
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| DOID:1184 | nephrotic syndrome | HGNC:23204 | Homo sapiens (human) | 84623 | KIRREL3 |
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| DOID:0060929 | non-syndromic X-linked intellectual developmental disorder 111 | HGNC:13449 | Homo sapiens (human) | 84631 | SLITRK2 |
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