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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:2256 | osteochondrodysplasia | HGNC:2218 | Homo sapiens (human) | 1298 | COL9A2 |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:2355 | anemia | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:783 | end stage renal disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:1926 | Gaucher's disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0070300 | multiple epiphyseal dysplasia 4 | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:9408 | acute myocardial infarction | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:10763 | hypertension | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:0111225 | centronuclear myopathy X-linked | HGNC:16825 | Homo sapiens (human) | 55613 | MTMR8 |
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| DOID:224 | transient cerebral ischemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:2841 | asthma | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:9970 | obesity | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:0060673 | Peters anomaly | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0110735 | neurodegeneration with brain iron accumulation 2a | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:3534 | Lafora disease | HGNC:21576 | Homo sapiens (human) | 378884 | NHLRC1 |
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| DOID:0050742 | nicotine dependence | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:0050865 | tongue squamous cell carcinoma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:1574 | alcohol use disorder | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:1485 | cystic fibrosis | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:7941 | Barrett's adenocarcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:5844 | myocardial infarction | HGNC:9952 | Homo sapiens (human) | 5968 | REG1B |
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| DOID:1094 | attention deficit hyperactivity disorder | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | HGNC:6172 | Homo sapiens (human) | 3703 | STT3A |
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