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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:1380 | endometrial cancer | HGNC:18185 | Homo sapiens (human) | 54206 | ERRFI1 |
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| DOID:8398 | osteoarthritis | HGNC:18185 | Homo sapiens (human) | 54206 | ERRFI1 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3125 | multiple endocrine neoplasia | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:11983 | Prader-Willi syndrome | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:783 | end stage renal disease | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:3525 | middle cerebral artery infarction | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:1287 | cardiovascular system disease | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:11981 | morbid obesity | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:9743 | diabetic neuropathy | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:9970 | obesity | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:0050848 | obstructive sleep apnea | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:0070268 | congenital disorder of glycosylation type IIp | HGNC:18085 | Homo sapiens (human) | 147007 | TMEM199 |
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| DOID:162 | cancer | HGNC:1801 | Homo sapiens (human) | 8760 | CDS2 |
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| DOID:162 | cancer | HGNC:1800 | Homo sapiens (human) | 1040 | CDS1 |
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| DOID:11724 | limb-girdle muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:12930 | dilated cardiomyopathy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0110299 | autosomal recessive limb-girdle muscular dystrophy type 2I | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:9884 | muscular dystrophy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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