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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:3083 | chronic obstructive pulmonary disease | HGNC:2596 | Homo sapiens (human) | 1544 | CYP1A2 |
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| DOID:422 | congenital structural myopathy | HGNC:7448 | Homo sapiens (human) | 4534 | MTM1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:4124 | Homo sapiens (human) | 2590 | GALNT2 |
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| DOID:0070330 | multiple mitochondrial dysfunctions syndrome | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:0080159 | Cryptococcal meningitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:10534 | stomach cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:2957 | pulmonary tuberculosis | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | HGNC:32456 | Homo sapiens (human) | 440138 | ALG11 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:9974 | drug dependence | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:0050741 | alcohol dependence | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:2256 | osteochondrodysplasia | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:8398 | osteoarthritis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:783 | end stage renal disease | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:1612 | breast cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:1993 | rectum cancer | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:10283 | prostate cancer | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:13001 | carotid stenosis | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:9256 | colorectal cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0111822 | CHILD syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:12377 | spinal muscular atrophy | HGNC:4879 | Homo sapiens (human) | 3074 | HEXB |
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| DOID:0050873 | follicular lymphoma | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:4852 | pleomorphic xanthoastrocytoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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