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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:11506 | suppurative otitis media | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:12236 | primary biliary cholangitis | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:12732 | intermediate uveitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10591 | pre-eclampsia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:11832 | visual epilepsy | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:2870 | endometrial adenocarcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:0060740 | methylmalonic aciduria due to methylmalonyl-CoA mutase deficiency | HGNC:7526 | Homo sapiens (human) | 4594 | MMUT |
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| DOID:0050817 | Stargardt disease | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:12365 | malaria | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0080379 | nephrotic syndrome type 2 | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:1123 | spondyloarthropathy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:417 | autoimmune disease | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:104 | bacterial infectious disease | HGNC:10661 | Homo sapiens (human) | 6385 | SDC4 |
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| DOID:0080630 | B-lymphoblastic leukemia/lymphoma | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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| DOID:9970 | obesity | HGNC:20113 | Homo sapiens (human) | 123099 | DEGS2 |
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| DOID:9970 | obesity | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:1324 | lung cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10763 | hypertension | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:3211 | lysosomal storage disease | HGNC:9498 | Homo sapiens (human) | 5660 | PSAP |
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| DOID:12129 | bulimia nervosa | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:9970 | obesity | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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