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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:809 | cocaine abuse | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:0112282 | spondyloepiphyseal dysplasia Kimberley type | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:2394 | ovarian cancer | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:0111242 | congenital muscular dystrophy-dystroglycanopathy type A6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:0050741 | alcohol dependence | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:9970 | obesity | HGNC:10660 | Homo sapiens (human) | 9672 | SDC3 |
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| DOID:9155 | mucocutaneous leishmaniasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:409 | liver disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:10763 | hypertension | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:10584 | retinitis pigmentosa | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0050073 | invasive aspergillosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:10754 | otitis media | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0080411 | familial adenomatous polyposis 3 | HGNC:8028 | Homo sapiens (human) | 4913 | NTHL1 |
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| DOID:0112319 | Kanzaki disease | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:5082 | liver cirrhosis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0110820 | hereditary spastic paraplegia 75 | HGNC:6783 | Homo sapiens (human) | 4099 | MAG |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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| DOID:2841 | asthma | HGNC:23064 | Homo sapiens (human) | 119391 | GSTO2 |
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| DOID:0070256 | congenital disorder of glycosylation type IId | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18619 | Homo sapiens (human) | 83548 | COG3 |
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| DOID:14735 | hereditary angioedema | HGNC:14178 | Homo sapiens (human) | 64711 | HS3ST6 |
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| DOID:14766 | renal agenesis | HGNC:4243 | Homo sapiens (human) | 2674 | GFRA1 |
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| DOID:7147 | ankylosing spondylitis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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