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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:0080540 | galactosialidosis | HGNC:9251 | Homo sapiens (human) | 5476 | CTSA |
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| DOID:3211 | lysosomal storage disease | HGNC:9251 | Homo sapiens (human) | 5476 | CTSA |
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| DOID:2986 | IgA glomerulonephritis | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:28 | endocrine system disease | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9238 | Homo sapiens (human) | 5471 | PPAT |
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| DOID:4450 | renal cell carcinoma | HGNC:9238 | Homo sapiens (human) | 5471 | PPAT |
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| DOID:5844 | myocardial infarction | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0060611 | abdominal obesity-metabolic syndrome | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:1287 | cardiovascular system disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:10376 | amblyopia | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050855 | renal fibrosis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:4195 | hyperglycemia | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:114 | heart disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:9970 | obesity | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:263 | kidney cancer | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:10652 | Alzheimer's disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:11446 | sciatic neuropathy | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:12236 | primary biliary cholangitis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0050328 | congenital hypothyroidism | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0060180 | colitis | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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