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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:684 | hepatocellular carcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:1380 | endometrial cancer | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:3033 | colon signet ring adenocarcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:10471 | Homo sapiens (human) | 861 | RUNX1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11374 | Homo sapiens (human) | 8614 | STC2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:10286 | prostate carcinoma | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:10283 | prostate cancer | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:1612 | breast cancer | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:1059 | intellectual disability | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:0112247 | congenital heart defects, dysmorphic facial features, and intellectual developmental disorder | HGNC:1733 | Homo sapiens (human) | 8621 | CDK13 |
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| DOID:0060419 | chromosome 3q29 microdeletion syndrome | HGNC:23316 | Homo sapiens (human) | 8630 | HSD17B6 |
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| DOID:0111926 | spermatogenic failure 39 | HGNC:2946 | Homo sapiens (human) | 8632 | DNAH17 |
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| DOID:10003 | sensorineural hearing loss | HGNC:2946 | Homo sapiens (human) | 8632 | DNAH17 |
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| DOID:1324 | lung cancer | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:5410 | pulmonary neuroendocrine tumor | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:3883 | Lynch syndrome | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:0081007 | RNASET2-deficient cystic leukoencephalopathy | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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