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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
LM-GlycoRepo
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:9655 | oral mucosa leukoplakia | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:2355 | anemia | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:14499 | Fabry disease | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:0060733 | junctional epidermolysis bullosa with pyloric atresia | HGNC:6142 | Homo sapiens (human) | 3655 | ITGA6 |
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| DOID:0110160 | Charcot-Marie-Tooth disease axonal type 2T | HGNC:7154 | Homo sapiens (human) | 4311 | MME |
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| DOID:11758 | iron deficiency anemia | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:0110444 | dilated cardiomyopathy 1X | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:1240 | leukemia | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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| DOID:0060679 | catecholaminergic polymorphic ventricular tachycardia 5 | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:3393 | coronary artery disease | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:0070201 | Miyoshi muscular dystrophy 3 | HGNC:27337 | Homo sapiens (human) | 203859 | ANO5 |
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| DOID:4440 | seminoma | HGNC:6407 | Homo sapiens (human) | 3845 | KRAS |
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| DOID:1059 | intellectual disability | HGNC:6050 | Homo sapiens (human) | 3612 | IMPA1 |
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| DOID:0110200 | Charcot-Marie-Tooth disease dominant intermediate D | HGNC:7225 | Homo sapiens (human) | 4359 | MPZ |
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| DOID:13189 | gout | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:29955 | Homo sapiens (human) | 200931 | SLC51A |
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| DOID:0080162 | lupus nephritis | HGNC:8760 | Homo sapiens (human) | 5133 | PDCD1 |
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| DOID:10534 | stomach cancer | HGNC:6024 | Homo sapiens (human) | 3575 | IL7R |
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| DOID:2841 | asthma | HGNC:6011 | Homo sapiens (human) | 3562 | IL3 |
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| DOID:417 | autoimmune disease | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0112121 | nephrogenic syndrome of inappropriate antidiuresis | HGNC:897 | Homo sapiens (human) | 554 | AVPR2 |
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| DOID:83 | cataract | HGNC:4118 | Homo sapiens (human) | 2584 | GALK1 |
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| DOID:0070043 | autosomal dominant intellectual developmental disorder 13 | HGNC:2961 | Homo sapiens (human) | 1778 | DYNC1H1 |
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