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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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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:5844 | myocardial infarction | HGNC:11934 | Homo sapiens (human) | 7292 | TNFSF4 |
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| DOID:0050753 | cerebellar ataxia | HGNC:20499 | Homo sapiens (human) | 79944 | L2HGDH |
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| DOID:1470 | major depressive disorder | HGNC:6018 | Homo sapiens (human) | 3569 | IL6 |
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| DOID:9146 | visceral leishmaniasis | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0080231 | autosomal dominant intellectual developmental disorder 52 | HGNC:19088 | Homo sapiens (human) | 55870 | ASH1L |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:6709 | Homo sapiens (human) | 4049 | LTA |
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| DOID:9119 | acute myeloid leukemia | HGNC:76 | Homo sapiens (human) | 25 | ABL1 |
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| DOID:321 | tropical spastic paraparesis | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:10763 | hypertension | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0111664 | ectodermal dysplasia 1 | HGNC:3157 | Homo sapiens (human) | 1896 | EDA |
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| DOID:9351 | diabetes mellitus | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:0081424 | familial focal epilepsy with variable foci 4 | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:576 | proteinuria | HGNC:320 | Homo sapiens (human) | 177 | AGER |
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| DOID:6419 | tetralogy of Fallot | HGNC:7432 | Homo sapiens (human) | 4522 | MTHFD1 |
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| DOID:1825 | childhood absence epilepsy | HGNC:18712 | Homo sapiens (human) | 163175 | LGI4 |
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| DOID:10286 | prostate carcinoma | HGNC:3273 | Homo sapiens (human) | 8667 | EIF3H |
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| DOID:0111841 | Shukla-Vernon syndrome | HGNC:25657 | Homo sapiens (human) | 63035 | BCORL1 |
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| DOID:1681 | heart septal defect | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:0050641 | Rh deficiency syndrome | HGNC:10006 | Homo sapiens (human) | 6005 | RHAG |
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| DOID:3234 | central nervous system lymphoma | HGNC:1699 | Homo sapiens (human) | 974 | CD79B |
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| DOID:0080787 | proximal symphalangism 1 | HGNC:7866 | Homo sapiens (human) | 9241 | NOG |
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| DOID:2671 | transitional cell carcinoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0111331 | intellectual disability-severe speech delay-mild dysmorphism syndrome | HGNC:3823 | Homo sapiens (human) | 27086 | FOXP1 |
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| DOID:0111363 | Heinz body anemia | HGNC:4823 | Homo sapiens (human) | 3039 | HBA1 |
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