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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:9744 | type 1 diabetes mellitus | HGNC:3575 | Homo sapiens (human) | 9415 | FADS2 |
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| DOID:104 | bacterial infectious disease | HGNC:11022 | Homo sapiens (human) | 7355 | SLC35A2 |
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| DOID:0112315 | brain small vessel disease 3 | HGNC:26182 | Homo sapiens (human) | 79709 | COLGALT1 |
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| DOID:14227 | azoospermia | HGNC:7682 | Homo sapiens (human) | 9348 | NDST3 |
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| DOID:1596 | depressive disorder | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:3146 | lipid metabolism disorder | HGNC:4803 | Homo sapiens (human) | 3032 | HADHB |
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| DOID:13359 | Ehlers-Danlos syndrome | HGNC:2705 | Homo sapiens (human) | 1634 | DCN |
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| DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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| DOID:10763 | hypertension | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0050833 | orotic aciduria | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:12930 | dilated cardiomyopathy | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:9408 | acute myocardial infarction | HGNC:5998 | Homo sapiens (human) | 9173 | IL1RL1 |
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| DOID:2747 | glycogen storage disease | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:10534 | stomach cancer | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:0050648 | atelosteogenesis | HGNC:10994 | Homo sapiens (human) | 1836 | SLC26A2 |
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| DOID:5419 | schizophrenia | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:3121 | gallbladder cancer | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:1289 | neurodegenerative disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:891 | progressive myoclonus epilepsy | HGNC:3413 | Homo sapiens (human) | 7957 | EPM2A |
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| DOID:783 | end stage renal disease | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0081267 | graft-versus-host disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0050729 | Chanarin-Dorfman syndrome | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:9538 | multiple myeloma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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