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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:783 | end stage renal disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:1099 | alpha thalassemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:3312 | bipolar disorder | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:4450 | renal cell carcinoma | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:4137 | common bile duct disease | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:10590 | mild pre-eclampsia | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10803 | Homo sapiens (human) | 6441 | SFTPD |
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| DOID:784 | chronic kidney disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:2377 | multiple sclerosis | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:2394 | ovarian cancer | HGNC:10850 | Homo sapiens (human) | 6470 | SHMT1 |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:10908 | hydrocephalus | HGNC:6470 | Homo sapiens (human) | 3897 | L1CAM |
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| DOID:2355 | anemia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:162 | cancer | HGNC:8898 | Homo sapiens (human) | 5232 | PGK2 |
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| DOID:0060224 | atrial fibrillation | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:576 | proteinuria | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:1380 | endometrial cancer | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:4362 | cervical cancer | HGNC:1753 | Homo sapiens (human) | 1012 | CDH13 |
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| DOID:10534 | stomach cancer | HGNC:5383 | Homo sapiens (human) | 3418 | IDH2 |
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| DOID:4194 | glucose metabolism disease | HGNC:23302 | Homo sapiens (human) | 80201 | HKDC1 |
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| DOID:1240 | leukemia | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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