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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:0060180 | colitis | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:0080533 | Carney-Stratakis syndrome | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:6088 | acute stress disorder | HGNC:108 | Homo sapiens (human) | 43 | ACHE |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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| DOID:3713 | ovary adenocarcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:13628 | favism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0080124 | mitochondrial DNA depletion syndrome 5 | HGNC:11448 | Homo sapiens (human) | 8803 | SUCLA2 |
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| DOID:1184 | nephrotic syndrome | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:423 | myopathy | HGNC:16781 | Homo sapiens (human) | 80896 | NPL |
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| DOID:10763 | hypertension | HGNC:17423 | Homo sapiens (human) | 55501 | CHST12 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:0111619 | combined D-2- and L-2-hydroxyglutaric aciduria | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0060496 | respiratory allergy | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:5082 | liver cirrhosis | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:418 | systemic scleroderma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:3071 | gliosarcoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050152 | aspiration pneumonia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:162 | cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0111156 | spermatogenic failure 9 | HGNC:19414 | Homo sapiens (human) | 283417 | DPY19L2 |
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| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:5138 | leiomyomatosis | HGNC:3700 | Homo sapiens (human) | 2271 | FH |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:583 | hemolytic anemia | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:2043 | hepatitis B | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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