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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:2394 | ovarian cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:303 | substance-related disorder | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:4247 | coronary restenosis | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:10283 | prostate cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:11054 | urinary bladder cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:0060728 | NGLY1-deficiency | HGNC:17646 | Homo sapiens (human) | 55768 | NGLY1 |
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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:4440 | seminoma | HGNC:17825 | Homo sapiens (human) | 11145 | PLAAT3 |
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| DOID:5679 | retinal disease | HGNC:17852 | Homo sapiens (human) | 56994 | CHPT1 |
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| DOID:10763 | hypertension | HGNC:17855 | Homo sapiens (human) | 26035 | GLCE |
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| DOID:6713 | cerebrovascular disease | HGNC:17855 | Homo sapiens (human) | 26035 | GLCE |
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| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
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| DOID:1793 | pancreatic cancer | HGNC:17968 | Homo sapiens (human) | 51146 | A4GNT |
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| DOID:0112198 | spondyloepimetaphyseal dysplasia with joint laxity type 1 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:17978 | Homo sapiens (human) | 126792 | B3GALT6 |
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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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