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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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MIRAGE
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:3910 | lung adenocarcinoma | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:1612 | breast cancer | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:9256 | colorectal cancer | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:0080909 | castration-resistant prostate carcinoma | HGNC:14621 | Homo sapiens (human) | 83540 | NUF2 |
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| DOID:10273 | heart conduction disease | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:1826 | epilepsy | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:1591 | renovascular hypertension | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:5844 | myocardial infarction | HGNC:1462 | Homo sapiens (human) | 817 | CAMK2D |
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| DOID:10273 | heart conduction disease | HGNC:1461 | Homo sapiens (human) | 816 | CAMK2B |
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| DOID:0080230 | autosomal dominant intellectual developmental disorder 54 | HGNC:1461 | Homo sapiens (human) | 816 | CAMK2B |
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| DOID:13382 | megaloblastic anemia | HGNC:14604 | Homo sapiens (human) | 81693 | AMN |
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| DOID:557 | kidney disease | HGNC:14604 | Homo sapiens (human) | 81693 | AMN |
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| DOID:0050700 | cardiomyopathy | HGNC:14604 | Homo sapiens (human) | 81693 | AMN |
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| DOID:3525 | middle cerebral artery infarction | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:3312 | bipolar disorder | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0060041 | autism spectrum disorder | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0080228 | autosomal dominant intellectual developmental disorder 53 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:10273 | heart conduction disease | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:10652 | Alzheimer's disease | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:224 | transient cerebral ischemia | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:3070 | high grade glioma | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0081224 | autosomal recessive intellectual developmental disorder 63 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:1909 | melanoma | HGNC:14587 | Homo sapiens (human) | 54556 | ING3 |
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