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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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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:8432 | polycythemia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:418 | systemic scleroderma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3770 | pulmonary fibrosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:12236 | primary biliary cholangitis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:3905 | lung carcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0060071 | pre-malignant neoplasm | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080569 | congenital disorder of glycosylation Ir | HGNC:2728 | Homo sapiens (human) | 1650 | DDOST |
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| DOID:0111263 | combined malonic and methylmalonic acidemia | HGNC:27288 | Homo sapiens (human) | 197322 | ACSF3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:27301 | Homo sapiens (human) | 200186 | CRTC2 |
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| DOID:0070267 | congenital disorder of glycosylation type IIo | HGNC:28178 | Homo sapiens (human) | 84317 | CCDC115 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:0110658 | congenital myasthenic syndrome 15 | HGNC:28287 | Homo sapiens (human) | 199857 | ALG14 |
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| DOID:0014667 | disease of metabolism | HGNC:28335 | Homo sapiens (human) | 160287 | LDHAL6A |
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| DOID:0080721 | calvarial doughnut lesions with bone fragility | HGNC:28395 | Homo sapiens (human) | 166929 | SGMS2 |
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| DOID:784 | chronic kidney disease | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:1184 | nephrotic syndrome | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:0050700 | cardiomyopathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:9970 | obesity | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:0060778 | congenital diarrhea 7 with exudative enteropathy | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:4194 | glucose metabolism disease | HGNC:2849 | Homo sapiens (human) | 1606 | DGKA |
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| DOID:4194 | glucose metabolism disease | HGNC:2850 | Homo sapiens (human) | 1607 | DGKB |
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| DOID:0050561 | Lennox-Gastaut syndrome | HGNC:2851 | Homo sapiens (human) | 8527 | DGKD |
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| DOID:0080388 | nephrotic syndrome type 7 | HGNC:2852 | Homo sapiens (human) | 8526 | DGKE |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:28526 | Homo sapiens (human) | 285203 | EOGT |
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| DOID:4194 | glucose metabolism disease | HGNC:2853 | Homo sapiens (human) | 1608 | DGKG |
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