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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:3908 | lung non-small cell carcinoma | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:5015 | fibrolamellar carcinoma | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:3883 | Lynch syndrome | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:0080199 | colorectal carcinoma | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:234 | colon adenocarcinoma | HGNC:1371 | Homo sapiens (human) | 771 | CA12 |
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| DOID:0070399 | hypomyelinating leukodystrophy 18 | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:9970 | obesity | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:1289 | neurodegenerative disease | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:0060786 | hypomyelinating leukodystrophy | HGNC:13709 | Homo sapiens (human) | 8560 | DEGS1 |
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| DOID:6432 | pulmonary hypertension | HGNC:13708 | Homo sapiens (human) | 11318 | GPR182 |
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| DOID:9970 | obesity | HGNC:13681 | Homo sapiens (human) | 8642 | DCHS1 |
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| DOID:988 | mitral valve prolapse | HGNC:13681 | Homo sapiens (human) | 8642 | DCHS1 |
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| DOID:0080585 | Van Maldergem syndrome 1 | HGNC:13681 | Homo sapiens (human) | 8642 | DCHS1 |
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| DOID:0050602 | triple-A syndrome | HGNC:13666 | Homo sapiens (human) | 8086 | AAAS |
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| DOID:9164 | achalasia | HGNC:13666 | Homo sapiens (human) | 8086 | AAAS |
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| DOID:0112228 | lissencephaly 9 with complex brainstem malformation | HGNC:13664 | Homo sapiens (human) | 23499 | MACF1 |
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| DOID:162 | cancer | HGNC:13664 | Homo sapiens (human) | 23499 | MACF1 |
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| DOID:10772 | thrombotic thrombocytopenic purpura | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:0080177 | hepatic veno-occlusive disease | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:13133 | HELLP syndrome | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:11247 | disseminated intravascular coagulation | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:5082 | liver cirrhosis | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:1366 | Homo sapiens (human) | 11093 | ADAMTS13 |
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