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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:1883 | hepatitis C | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:8577 | ulcerative colitis | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:0050524 | maturity-onset diabetes of the young | HGNC:11621 | Homo sapiens (human) | 6927 | HNF1A |
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| DOID:8577 | ulcerative colitis | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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| DOID:0081118 | benign familial infantile seizures 5 | HGNC:10596 | Homo sapiens (human) | 6334 | SCN8A |
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| DOID:8947 | diabetic retinopathy | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0081157 | dilated cardiomyopathy 1LL | HGNC:14000 | Homo sapiens (human) | 63976 | PRDM16 |
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| DOID:4890 | juvenile myoclonic epilepsy | HGNC:1103 | Homo sapiens (human) | 6046 | BRD2 |
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| DOID:0110540 | autosomal recessive nonsyndromic deafness 98 | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:1024 | leprosy | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:2033 | communication disorder | HGNC:2213 | Homo sapiens (human) | 1293 | COL6A3 |
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| DOID:0111422 | familial lipase maturation factor 1 deficiency | HGNC:14154 | Homo sapiens (human) | 64788 | LMF1 |
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| DOID:987 | alopecia | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:1287 | cardiovascular system disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:2152 | ovary epithelial cancer | HGNC:376 | Homo sapiens (human) | 9472 | AKAP6 |
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| DOID:5419 | schizophrenia | HGNC:2516 | Homo sapiens (human) | 1501 | CTNND2 |
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| DOID:10652 | Alzheimer's disease | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:824 | periodontitis | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:3255 | Homo sapiens (human) | 9451 | EIF2AK3 |
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| DOID:1612 | breast cancer | HGNC:3528 | Homo sapiens (human) | 2159 | F10 |
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| DOID:1380 | endometrial cancer | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:5844 | myocardial infarction | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
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| DOID:0002116 | pterygium | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:848 | arthritis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0060903 | thrombosis | HGNC:3529 | Homo sapiens (human) | 2160 | F11 |
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