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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:0081230 | autosomal recessive intellectual developmental disorder 69 | HGNC:16740 | Homo sapiens (human) | 27107 | ZBTB11 |
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| DOID:2048 | autoimmune hepatitis | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:10763 | hypertension | HGNC:6080 | Homo sapiens (human) | 3636 | INPPL1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:3689 | Homo sapiens (human) | 2263 | FGFR2 |
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| DOID:0081153 | common variable immunodeficiency 11 | HGNC:6005 | Homo sapiens (human) | 59067 | IL21 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:8893 | psoriasis | HGNC:11365 | Homo sapiens (human) | 6775 | STAT4 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:8063 | Homo sapiens (human) | 9631 | NUP155 |
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| DOID:11335 | sarcoidosis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:1884 | viral hepatitis | HGNC:6001 | Homo sapiens (human) | 3558 | IL2 |
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| DOID:1470 | major depressive disorder | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:0112300 | spondylometaphyseal dysplasia with cone-rod dystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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| DOID:4239 | alveolar soft part sarcoma | HGNC:13825 | Homo sapiens (human) | 79058 | ASPSCR1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:6250 | Homo sapiens (human) | 3756 | KCNH1 |
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| DOID:8432 | polycythemia | HGNC:3374 | Homo sapiens (human) | 2034 | EPAS1 |
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| DOID:0080549 | Noonan syndrome with multiple lentigines 2 | HGNC:9829 | Homo sapiens (human) | 5894 | RAF1 |
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| DOID:1793 | pancreatic cancer | HGNC:16696 | Homo sapiens (human) | 22938 | SNW1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:11180 | Homo sapiens (human) | 6648 | SOD2 |
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| DOID:0081141 | agammaglobulinemia 9 | HGNC:4927 | Homo sapiens (human) | 7922 | SLC39A7 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:29013 | Homo sapiens (human) | 23274 | CLEC16A |
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| DOID:2671 | transitional cell carcinoma | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:1657 | ventricular septal defect | HGNC:7775 | Homo sapiens (human) | 4772 | NFATC1 |
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| DOID:9074 | systemic lupus erythematosus | HGNC:11851 | Homo sapiens (human) | 7100 | TLR5 |
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| DOID:1681 | heart septal defect | HGNC:1078 | Homo sapiens (human) | 659 | BMPR2 |
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| DOID:7148 | rheumatoid arthritis | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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