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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: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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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:14115 | toxic shock syndrome | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0090064 | familial cold autoinflammatory syndrome 3 | HGNC:9066 | Homo sapiens (human) | 5336 | PLCG2 |
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| DOID:0070435 | hyperphosphatasia with impaired intellectual development syndrome 3 | HGNC:17893 | Homo sapiens (human) | 27315 | PGAP2 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0080382 | nephrotic syndrome type 3 | HGNC:17175 | Homo sapiens (human) | 51196 | PLCE1 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:0070460 | hereditary spastic paraplegia 90B | HGNC:20361 | Homo sapiens (human) | 171546 | SPTSSA |
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| DOID:0060639 | permanent neonatal diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:0112002 | immunodeficiency 47 | HGNC:868 | Homo sapiens (human) | 537 | ATP6AP1 |
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