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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0081317 | multiple synostoses syndrome 1 | HGNC:4220 | Homo sapiens (human) | 8200 | GDF5 |
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| DOID:1574 | alcohol use disorder | HGNC:7997 | Homo sapiens (human) | 3084 | NRG1 |
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| DOID:0111230 | congenital muscular dystrophy-dystroglycanopathy type A11 | HGNC:28596 | Homo sapiens (human) | 148789 | B3GALNT2 |
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| DOID:0050741 | alcohol dependence | HGNC:3262 | Homo sapiens (human) | 26523 | AGO1 |
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| DOID:0110946 | autosomal recessive osteopetrosis 7 | HGNC:11908 | Homo sapiens (human) | 8792 | TNFRSF11A |
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| DOID:0060224 | atrial fibrillation | HGNC:493 | Homo sapiens (human) | 287 | ANK2 |
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| DOID:0111463 | cardiofaciocutaneous syndrome 4 | HGNC:6842 | Homo sapiens (human) | 5605 | MAP2K2 |
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| DOID:2316 | brain ischemia | HGNC:5233 | Homo sapiens (human) | 3304 | HSPA1B |
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| DOID:0081220 | autosomal recessive intellectual developmental disorder 58 | HGNC:18248 | Homo sapiens (human) | 55250 | ELP2 |
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| DOID:1070 | primary open angle glaucoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:11335 | sarcoidosis | HGNC:1142 | Homo sapiens (human) | 56244 | BTNL2 |
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| DOID:77 | gastrointestinal system disease | HGNC:12663 | Homo sapiens (human) | 7412 | VCAM1 |
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| DOID:0060901 | lymphoplasmacytic lymphoma | HGNC:3619 | Homo sapiens (human) | 2214 | FCGR3A |
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| DOID:8577 | ulcerative colitis | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:1584 | acute chest syndrome | HGNC:7876 | Homo sapiens (human) | 4846 | NOS3 |
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| DOID:783 | end stage renal disease | HGNC:11078 | Homo sapiens (human) | 6553 | SLC9A5 |
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| DOID:0112091 | nuclear type mitochondrial complex I deficiency 34 | HGNC:33551 | Homo sapiens (human) | 284184 | NDUFAF8 |
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| DOID:1098 | fetal erythroblastosis | HGNC:3616 | Homo sapiens (human) | 2212 | FCGR2A |
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| DOID:2841 | asthma | HGNC:4502 | Homo sapiens (human) | 11251 | PTGDR2 |
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| DOID:891 | progressive myoclonus epilepsy | HGNC:10739 | Homo sapiens (human) | 10501 | SEMA6B |
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| DOID:9246 | cerebral amyloid angiopathy | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:0111999 | immunodeficiency 61 | HGNC:13867 | Homo sapiens (human) | 30011 | SH3KBP1 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0111576 | dehydrated hereditary stomatocytosis 1 | HGNC:28993 | Homo sapiens (human) | 9780 | PIEZO1 |
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| DOID:2349 | arteriosclerosis | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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