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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:4586 | familial meningioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:2893 | cervix carcinoma | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:4013 | Homo sapiens (human) | 2524 | FUT2 |
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| DOID:83 | cataract | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:3454 | brain infarction | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0080464 | developmental and epileptic encephalopathy 53 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:4988 | alcoholic pancreatitis | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:0060577 | 3MC syndrome 3 | HGNC:2220 | Homo sapiens (human) | 10584 | COLEC10 |
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| DOID:0080950 | alopecia-mental retardation syndrome 4 | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:0050773 | paraganglioma | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:9351 | diabetes mellitus | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:57 | aortic valve insufficiency | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0111238 | congenital muscular dystrophy-dystroglycanopathy type A13 | HGNC:15685 | Homo sapiens (human) | 11041 | B4GAT1 |
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| DOID:12549 | hepatitis A | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9074 | systemic lupus erythematosus | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:9970 | obesity | HGNC:2843 | Homo sapiens (human) | 8694 | DGAT1 |
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| DOID:9351 | diabetes mellitus | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:0111633 | congenital sucrase-isomaltase deficiency | HGNC:10856 | Homo sapiens (human) | 6476 | SI |
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| DOID:13166 | allergic bronchopulmonary aspergillosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:612 | primary immunodeficiency disease | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:10763 | hypertension | RGD:621503 | Rattus norvegicus (Norway rat) | 84020 | Kcnq1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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