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GlyTouCan
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
LM-GlycoRepo
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:0050569 | Seckel syndrome | HGNC:18672 | Homo sapiens (human) | 55755 | CDK5RAP2 |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:9314 | Homo sapiens (human) | 5530 | PPP3CA |
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| DOID:5082 | liver cirrhosis | HGNC:2433 | Homo sapiens (human) | 1436 | CSF1R |
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| DOID:0001816 | angiosarcoma | HGNC:7553 | Homo sapiens (human) | 4609 | MYC |
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| DOID:10608 | celiac disease | HGNC:5438 | Homo sapiens (human) | 3458 | IFNG |
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| DOID:0080016 | spina bifida | HGNC:4318 | Homo sapiens (human) | 2736 | GLI2 |
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| DOID:0080016 | spina bifida | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:0080016 | spina bifida | HGNC:4317 | Homo sapiens (human) | 2735 | GLI1 |
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| DOID:2526 | prostate adenocarcinoma | HGNC:6091 | Homo sapiens (human) | 3643 | INSR |
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| DOID:824 | periodontitis | RGD:631365 | Rattus norvegicus (Norway rat) | 297508 | Nampt |
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| DOID:8552 | chronic myeloid leukemia | HGNC:3113 | Homo sapiens (human) | 1869 | E2F1 |
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| DOID:5419 | schizophrenia | HGNC:3823 | Homo sapiens (human) | 27086 | FOXP1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:13177 | Homo sapiens (human) | 22807 | IKZF2 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:2515 | Homo sapiens (human) | 1500 | CTNND1 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:16921 | Homo sapiens (human) | 116986 | AGAP2 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:1748 | Homo sapiens (human) | 999 | CDH1 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1928 | Williams-Beuren syndrome | MGI:98397 | Mus musculus (house mouse) | 20779 | Src |
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| DOID:9261 | nasopharynx carcinoma | HGNC:4004 | Homo sapiens (human) | 8880 | FUBP1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1541 | Homo sapiens (human) | 867 | CBL |
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| DOID:12177 | common variable immunodeficiency | HGNC:17642 | Homo sapiens (human) | 64421 | DCLRE1C |
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| DOID:9408 | acute myocardial infarction | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:0050908 | myelodysplastic syndrome | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:11896 | Homo sapiens (human) | 7128 | TNFAIP3 |
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| DOID:4947 | cholangiocarcinoma | HGNC:19391 | Homo sapiens (human) | 9021 | SOCS3 |
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