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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:9352 | type 2 diabetes mellitus | HGNC:2623 | Homo sapiens (human) | 1559 | CYP2C9 |
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| DOID:1205 | allergic disease | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:594 | panic disorder | HGNC:1571 | Homo sapiens (human) | 887 | CCKBR |
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| DOID:0080020 | Jansen's metaphyseal chondrodysplasia | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:14866 | Homo sapiens (human) | 64399 | HHIP |
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| DOID:1205 | allergic disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0050578 | occult macular dystrophy | HGNC:15946 | Homo sapiens (human) | 94137 | RP1L1 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:9177 | Homo sapiens (human) | 5426 | POLE |
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| DOID:11123 | Henoch-Schoenlein purpura | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080177 | hepatic veno-occlusive disease | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:9646 | Homo sapiens (human) | 5783 | PTPN13 |
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| DOID:3407 | carotid artery disease | HGNC:3662 | Homo sapiens (human) | 2244 | FGB |
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| DOID:0060227 | Adams-Oliver syndrome | HGNC:29216 | Homo sapiens (human) | 57514 | ARHGAP31 |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:1331 | Homo sapiens (human) | 727 | C5 |
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| DOID:1324 | lung cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0050458 | juvenile myelomonocytic leukemia | HGNC:6193 | Homo sapiens (human) | 3718 | JAK3 |
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| DOID:0060300 | complement component 7 deficiency | HGNC:1346 | Homo sapiens (human) | 730 | C7 |
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| DOID:0111765 | X-linked cardiac valvular dysplasia | HGNC:3754 | Homo sapiens (human) | 2316 | FLNA |
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| DOID:5409 | lung small cell carcinoma | HGNC:6483 | Homo sapiens (human) | 3909 | LAMA3 |
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| DOID:5419 | schizophrenia | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:1059 | intellectual disability | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:12755 | Homo sapiens (human) | 10885 | WDR3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:0050957 | spinocerebellar ataxia type 4 | HGNC:777 | Homo sapiens (human) | 463 | ZFHX3 |
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