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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
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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:3393 | coronary artery disease | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9351 | diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0070216 | familial hyperinsulinemic hypoglycemia 3 | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:13317 | hyperinsulinemic hypoglycemia | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9993 | hypoglycemia | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9452 | steatotic liver disease | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9970 | obesity | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0050524 | maturity-onset diabetes of the young | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:11714 | gestational diabetes | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:0060639 | permanent neonatal diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:4194 | glucose metabolism disease | MGI:1270854 | Mus musculus (house mouse) | 103988 | Gck |
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| DOID:162 | cancer | HGNC:1800 | Homo sapiens (human) | 1040 | CDS1 |
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| DOID:0050127 | sinusitis | MGI:1341098 | Mus musculus (house mouse) | 104183 | Chil4 |
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| DOID:2841 | asthma | MGI:1341098 | Mus musculus (house mouse) | 104183 | Chil4 |
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| DOID:162 | cancer | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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| DOID:9452 | steatotic liver disease | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:3454 | brain infarction | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0070261 | congenital disorder of glycosylation type IIi | HGNC:14857 | Homo sapiens (human) | 10466 | COG5 |
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| DOID:3534 | Lafora disease | MGI:2145264 | Mus musculus (house mouse) | 105193 | Nhlrc1 |
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| DOID:811 | lipodystrophy | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0111135 | congenital generalized lipodystrophy type 1 | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0070152 | hereditary sensory and autonomic neuropathy type 1A | HGNC:11277 | Homo sapiens (human) | 10558 | SPTLC1 |
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