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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:783 | end stage renal disease | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:0050445 | X-linked dominant hypophosphatemic rickets | MGI:107489 | Mus musculus (house mouse) | 18675 | Phex |
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| DOID:8432 | polycythemia | HGNC:3416 | Homo sapiens (human) | 2057 | EPOR |
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| DOID:6000 | congestive heart failure | HGNC:3146 | Homo sapiens (human) | 1889 | ECE1 |
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| DOID:0110831 | Usher syndrome type 1D | MGI:1890219 | Mus musculus (house mouse) | 22295 | Cdh23 |
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| DOID:0090110 | immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | MGI:1891436 | Mus musculus (house mouse) | 20371 | Foxp3 |
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| DOID:1184 | nephrotic syndrome | MGI:1859637 | Mus musculus (house mouse) | 54631 | Nphs1 |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:8398 | osteoarthritis | HGNC:7159 | Homo sapiens (human) | 4322 | MMP13 |
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| DOID:9521 | Laron syndrome | MGI:95708 | Mus musculus (house mouse) | 14600 | Ghr |
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| DOID:3526 | cerebral infarction | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12519 | Homo sapiens (human) | 7352 | UCP3 |
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| DOID:5419 | schizophrenia | HGNC:9957 | Homo sapiens (human) | 5649 | RELN |
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| DOID:3265 | chronic granulomatous disease | HGNC:2578 | Homo sapiens (human) | 1536 | CYBB |
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| DOID:3068 | glioblastoma | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
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| DOID:3068 | glioblastoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050453 | lissencephaly | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:4450 | renal cell carcinoma | RGD:2458 | Rattus norvegicus (Norway rat) | 24296 | Cyp1a1 |
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| DOID:0050590 | severe congenital neutropenia | HGNC:2439 | Homo sapiens (human) | 1441 | CSF3R |
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| DOID:12930 | dilated cardiomyopathy | HGNC:7577 | Homo sapiens (human) | 4625 | MYH7 |
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| DOID:12387 | nephrogenic diabetes insipidus | MGI:88123 | Mus musculus (house mouse) | 12000 | Avpr2 |
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| DOID:6000 | congestive heart failure | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0090019 | sitosterolemia | HGNC:13887 | Homo sapiens (human) | 64241 | ABCG8 |
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| DOID:0050699 | Dent disease | MGI:99486 | Mus musculus (house mouse) | 12728 | Clcn5 |
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| DOID:0080053 | Albright's hereditary osteodystrophy | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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