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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
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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:224 | transient cerebral ischemia | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:0112231 | lissencephaly 7 with cerebellar hypoplasia | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:12098 | trigeminal neuralgia | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:2316 | brain ischemia | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:1826 | epilepsy | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:0050453 | lissencephaly | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:1596 | depressive disorder | HGNC:1774 | Homo sapiens (human) | 1020 | CDK5 |
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| DOID:0050453 | lissencephaly | HGNC:14434 | Homo sapiens (human) | 65061 | CDK15 |
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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:3717 | gastric adenocarcinoma | HGNC:24224 | Homo sapiens (human) | 51755 | CDK12 |
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| DOID:684 | hepatocellular carcinoma | HGNC:24224 | Homo sapiens (human) | 51755 | CDK12 |
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| DOID:10534 | stomach cancer | HGNC:24224 | Homo sapiens (human) | 51755 | CDK12 |
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| DOID:162 | cancer | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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| DOID:9452 | steatotic liver disease | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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| DOID:0111021 | cone-rod dystrophy 15 | HGNC:14550 | Homo sapiens (human) | 92211 | CDHR1 |
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| DOID:0050535 | exudative vitreoretinopathy | HGNC:1764 | Homo sapiens (human) | 1003 | CDH5 |
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| DOID:3963 | thyroid gland carcinoma | HGNC:1764 | Homo sapiens (human) | 1003 | CDH5 |
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| DOID:3393 | coronary artery disease | HGNC:1764 | Homo sapiens (human) | 1003 | CDH5 |
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| DOID:6432 | pulmonary hypertension | HGNC:1764 | Homo sapiens (human) | 1003 | CDH5 |
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