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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:0060558 | lethal congenital contracture syndrome | HGNC:8011 | Homo sapiens (human) | 8506 | CNTNAP1 |
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| DOID:5602 | T-cell adult acute lymphocytic leukemia | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:3070 | high grade glioma | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:850 | lung disease | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0080101 | Compton-North congenital myopathy | HGNC:2171 | Homo sapiens (human) | 1272 | CNTN1 |
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| DOID:2030 | anxiety disorder | HGNC:2160 | Homo sapiens (human) | 1269 | CNR2 |
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| DOID:4989 | pancreatitis | HGNC:2160 | Homo sapiens (human) | 1269 | CNR2 |
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| DOID:848 | arthritis | HGNC:2160 | Homo sapiens (human) | 1269 | CNR2 |
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| DOID:12858 | Huntington's disease | HGNC:2160 | Homo sapiens (human) | 1269 | CNR2 |
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| DOID:11446 | sciatic neuropathy | HGNC:2160 | Homo sapiens (human) | 1269 | CNR2 |
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| DOID:750 | peptic ulcer disease | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:0080855 | Parkinsonism | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:5419 | schizophrenia | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:2234 | focal epilepsy | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:9970 | obesity | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:1574 | alcohol use disorder | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:9743 | diabetic neuropathy | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:1875 | impotence | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:10763 | hypertension | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:1824 | status epilepticus | HGNC:2159 | Homo sapiens (human) | 1268 | CNR1 |
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| DOID:0080432 | developmental and epileptic encephalopathy 60 | HGNC:11968 | Homo sapiens (human) | 10695 | CNPY3 |
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| DOID:114 | heart disease | HGNC:18042 | Homo sapiens (human) | 246175 | CNOT6L |
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| DOID:114 | heart disease | HGNC:7880 | Homo sapiens (human) | 4850 | CNOT4 |
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