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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:4947 | cholangiocarcinoma | HGNC:22950 | Homo sapiens (human) | 80243 | PREX2 |
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| DOID:2043 | hepatitis B | HGNC:22950 | Homo sapiens (human) | 80243 | PREX2 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:22950 | Homo sapiens (human) | 80243 | PREX2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:22950 | Homo sapiens (human) | 80243 | PREX2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:22950 | Homo sapiens (human) | 80243 | PREX2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:16787 | Homo sapiens (human) | 80267 | EDEM3 |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:9256 | colorectal cancer | HGNC:14897 | Homo sapiens (human) | 80271 | ITPKC |
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| DOID:8864 | acute monocytic leukemia | HGNC:16063 | Homo sapiens (human) | 8028 | MLLT10 |
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| DOID:9119 | acute myeloid leukemia | HGNC:16063 | Homo sapiens (human) | 8028 | MLLT10 |
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| DOID:104 | bacterial infectious disease | MGI:1933134 | Mus musculus (house mouse) | 80286 | Tusc3 |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | MGI:1933134 | Mus musculus (house mouse) | 80286 | Tusc3 |
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| DOID:10283 | prostate cancer | MGI:1933134 | Mus musculus (house mouse) | 80286 | Tusc3 |
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| DOID:0060411 | chromosome 1q21.1 deletion syndrome | MGI:1933114 | Mus musculus (house mouse) | 80288 | Bcl9l |
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| DOID:3393 | coronary artery disease | HGNC:2548 | Homo sapiens (human) | 8029 | CUBN |
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| DOID:557 | kidney disease | HGNC:2548 | Homo sapiens (human) | 8029 | CUBN |
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| DOID:10591 | pre-eclampsia | HGNC:2548 | Homo sapiens (human) | 8029 | CUBN |
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| DOID:14250 | Down syndrome | MGI:1916863 | Mus musculus (house mouse) | 80294 | Pofut2 |
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| DOID:10283 | prostate cancer | HGNC:7671 | Homo sapiens (human) | 8031 | NCOA4 |
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| DOID:3008 | invasive ductal carcinoma | HGNC:7671 | Homo sapiens (human) | 8031 | NCOA4 |
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| DOID:4001 | ovarian carcinoma | HGNC:7671 | Homo sapiens (human) | 8031 | NCOA4 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:7671 | Homo sapiens (human) | 8031 | NCOA4 |
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| DOID:10286 | prostate carcinoma | HGNC:30620 | Homo sapiens (human) | 80310 | PDGFD |
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| DOID:5844 | myocardial infarction | HGNC:30620 | Homo sapiens (human) | 80310 | PDGFD |
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