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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:13207 | proliferative diabetic retinopathy | HGNC:9922 | Homo sapiens (human) | 5950 | RBP4 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:6364 | migraine | RGD:71034 | Rattus norvegicus (Norway rat) | 65032 | Htr7 |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:12373 | Homo sapiens (human) | 7253 | TSHR |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2593 | Homo sapiens (human) | 1586 | CYP17A1 |
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| DOID:5419 | schizophrenia | HGNC:13759 | Homo sapiens (human) | 23191 | CYFIP1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:8941 | Homo sapiens (human) | 5265 | SERPINA1 |
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| DOID:2841 | asthma | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:11054 | urinary bladder cancer | HGNC:11785 | Homo sapiens (human) | 7057 | THBS1 |
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| DOID:552 | pneumonia | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1324 | lung cancer | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1936 | atherosclerosis | HGNC:6667 | Homo sapiens (human) | 4018 | LPA |
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| DOID:2234 | focal epilepsy | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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| DOID:1825 | childhood absence epilepsy | RGD:621320 | Rattus norvegicus (Norway rat) | 81687 | Mmp9 |
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| DOID:3798 | pleural empyema | HGNC:9052 | Homo sapiens (human) | 5328 | PLAU |
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| DOID:8552 | chronic myeloid leukemia | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:10923 | sickle cell anemia | HGNC:8823 | Homo sapiens (human) | 5175 | PECAM1 |
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| DOID:768 | retinoblastoma | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:3382 | liposarcoma | HGNC:4010 | Homo sapiens (human) | 2521 | FUS |
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| DOID:4989 | pancreatitis | RGD:2887 | Rattus norvegicus (Norway rat) | 25670 | Il15 |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:3583 | Homo sapiens (human) | 2187 | FANCB |
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| DOID:0081120 | Graves ophthalmopathy | HGNC:6011 | Homo sapiens (human) | 3562 | IL3 |
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| DOID:12361 | Graves' disease | HGNC:6011 | Homo sapiens (human) | 3562 | IL3 |
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| DOID:1062 | Fanconi syndrome | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0060738 | junctional epidermolysis bullosa non-Herlitz type | MGI:99913 | Mus musculus (house mouse) | 16782 | Lamc2 |
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