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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:9261 | nasopharynx carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0050985 | spinocerebellar ataxia type 38 | HGNC:21308 | Homo sapiens (human) | 60481 | ELOVL5 |
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| DOID:10584 | retinitis pigmentosa | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:0050719 | cerebral folate receptor alpha deficiency | HGNC:3791 | Homo sapiens (human) | 2348 | FOLR1 |
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| DOID:4607 | biliary tract cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:3393 | coronary artery disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:9743 | diabetic neuropathy | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0112127 | HRPT-related hyperuricemia | HGNC:5157 | Homo sapiens (human) | 3251 | HPRT1 |
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| DOID:9775 | diastolic heart failure | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:0110443 | dilated cardiomyopathy 1B | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:0070174 | spermatogenic failure 17 | HGNC:19218 | Homo sapiens (human) | 89869 | PLCZ1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:2747 | glycogen storage disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:8552 | chronic myeloid leukemia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0050573 | 2-hydroxyglutaric aciduria | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:4989 | pancreatitis | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:3651 | pyruvate carboxylase deficiency disease | HGNC:8636 | Homo sapiens (human) | 5091 | PC |
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| DOID:3393 | coronary artery disease | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:1984 | rectal benign neoplasm | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:2747 | glycogen storage disease | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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| DOID:5419 | schizophrenia | HGNC:18601 | Homo sapiens (human) | 65078 | RTN4R |
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| DOID:2316 | brain ischemia | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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