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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:0111162 | epidermal nevus | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:13375 | temporal arteritis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:4398 | pustulosis of palm and sole | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:6000 | congestive heart failure | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:13544 | low tension glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050741 | alcohol dependence | HGNC:4093 | Homo sapiens (human) | 2572 | GAD2 |
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| DOID:12678 | hypercalcemia | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:2383 | neonatal jaundice | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:2352 | hemochromatosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080128 | mitochondrial DNA depletion syndrome 9 | HGNC:11449 | Homo sapiens (human) | 8802 | SUCLG1 |
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| DOID:6713 | cerebrovascular disease | HGNC:10718 | Homo sapiens (human) | 6401 | SELE |
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| DOID:0060653 | lethal congenital contracture syndrome 3 | HGNC:8996 | Homo sapiens (human) | 23396 | PIP5K1C |
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| DOID:0111402 | mucopolysaccharidosis type IIID | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:10763 | hypertension | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:2606 | Homo sapiens (human) | 1594 | CYP27B1 |
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| DOID:1067 | open-angle glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:2349 | arteriosclerosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5467 | Homo sapiens (human) | 3482 | IGF2R |
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| DOID:1574 | alcohol use disorder | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:9351 | diabetes mellitus | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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