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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:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:9256 | colorectal cancer | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:0080000 | muscular disease | HGNC:3594 | Homo sapiens (human) | 2194 | FASN |
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| DOID:5204 | fructose-1,6-bisphosphatase deficiency | HGNC:3606 | Homo sapiens (human) | 2203 | FBP1 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0110284 | autosomal recessive limb-girdle muscular dystrophy type 2L | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0110444 | dilated cardiomyopathy 1X | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0110443 | dilated cardiomyopathy 1B | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0110296 | autosomal recessive limb-girdle muscular dystrophy type 2M | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:9884 | muscular dystrophy | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:83 | cataract | HGNC:3629 | Homo sapiens (human) | 2222 | FDFT1 |
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| DOID:3805 | porokeratosis | HGNC:3631 | Homo sapiens (human) | 2224 | FDPS |
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| DOID:0111261 | fumarase deficiency | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:5138 | leiomyomatosis | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:0080563 | congenital disorder of glycosylation Ik | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:0110295 | autosomal recessive limb-girdle muscular dystrophy type 2U | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:0111234 | congenital muscular dystrophy-dystroglycanopathy A7 | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:824 | periodontitis | HGNC:3774 | Homo sapiens (human) | 2331 | FMOD |
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