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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: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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| DOID:2986 | IgA glomerulonephritis | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:3008 | invasive ductal carcinoma | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0070395 | developmental and epileptic encephalopathy 110 | HGNC:1399 | Homo sapiens (human) | 781 | CACNA2D1 |
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| DOID:11613 | hyperandrogenism | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:14330 | Parkinson's disease | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:0060001 | withdrawal disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:14330 | Parkinson's disease | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:12241 | beta thalassemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:0111313 | idiopathic generalized epilepsy 12 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:9970 | obesity | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:1380 | endometrial cancer | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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