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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: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:14501 | Sjogren-Larsson syndrome | HGNC:411 | Homo sapiens (human) | 222 | ALDH3B2 |
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| DOID:83 | cataract | HGNC:3629 | Homo sapiens (human) | 2222 | FDFT1 |
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| DOID:1459 | hypothyroidism | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:13603 | obstructive jaundice | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:10763 | hypertension | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:9970 | obesity | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:9452 | steatotic liver disease | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:9743 | diabetic neuropathy | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:12858 | Huntington's disease | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:0050770 | polycystic liver disease | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:9352 | type 2 diabetes mellitus | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:783 | end stage renal disease | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:3407 | carotid artery disease | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:6000 | congestive heart failure | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:224 | transient cerebral ischemia | MGI:109354 | Mus musculus (house mouse) | 22228 | Ucp2 |
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| DOID:10763 | hypertension | MGI:1332243 | Mus musculus (house mouse) | 22234 | Ugcg |
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| DOID:3805 | porokeratosis | HGNC:3631 | Homo sapiens (human) | 2224 | FDPS |
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