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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:13810 | familial hypercholesterolemia | HGNC:20001 | Homo sapiens (human) | 255738 | PCSK9 |
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| DOID:2723 | dermatitis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:0080352 | X-linked chondrodysplasia punctata 2 | HGNC:3133 | Homo sapiens (human) | 10682 | EBP |
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| DOID:0081209 | autosomal recessive intellectual developmental disorder 45 | HGNC:16510 | Homo sapiens (human) | 79791 | FBXO31 |
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| DOID:4606 | bile duct cancer | HGNC:603 | Homo sapiens (human) | 338 | APOB |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:1612 | breast cancer | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:5844 | myocardial infarction | HGNC:8602 | Homo sapiens (human) | 5069 | PAPPA |
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| DOID:3181 | oligodendroglioma | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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| DOID:5844 | myocardial infarction | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:8552 | chronic myeloid leukemia | HGNC:74 | Homo sapiens (human) | 9429 | ABCG2 |
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| DOID:1936 | atherosclerosis | HGNC:243 | Homo sapiens (human) | 118 | ADD1 |
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| DOID:10933 | obsessive-compulsive disorder | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:9296 | cleft lip | HGNC:10659 | Homo sapiens (human) | 6383 | SDC2 |
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| DOID:10591 | pre-eclampsia | HGNC:2095 | Homo sapiens (human) | 1191 | CLU |
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| DOID:0080776 | partial androgen insensitivity syndrome | HGNC:644 | Homo sapiens (human) | 367 | AR |
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| DOID:1059 | intellectual disability | HGNC:2928 | Homo sapiens (human) | 1756 | DMD |
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| DOID:0110543 | autosomal dominant nonsyndromic deafness 11 | HGNC:7606 | Homo sapiens (human) | 4647 | MYO7A |
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| DOID:219 | colon cancer | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:12859 | choreatic disease | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:9869 | hereditary fructose intolerance syndrome | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:1882 | atrial heart septal defect | HGNC:4173 | Homo sapiens (human) | 2626 | GATA4 |
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| DOID:3319 | lymphangioleiomyomatosis | HGNC:12363 | Homo sapiens (human) | 7249 | TSC2 |
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| DOID:0110290 | autosomal recessive limb-girdle muscular dystrophy type 2X | HGNC:1152 | Homo sapiens (human) | 11149 | POPDC1 |
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| DOID:1793 | pancreatic cancer | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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