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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:0081400 | autosomal dominant distal hereditary motor neuronopathy 11 | HGNC:11273 | Homo sapiens (human) | 6709 | SPTAN1 |
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| DOID:0110916 | hereditary spherocytosis type 1 | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:10923 | sickle cell anemia | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:0110918 | hereditary spherocytosis type 3 | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:12971 | hereditary spherocytosis | HGNC:11272 | Homo sapiens (human) | 6708 | SPTA1 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:0060340 | ciliopathy | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:0080072 | intestinal pseudo-obstruction | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:9164 | achalasia | HGNC:11270 | Homo sapiens (human) | 10253 | SPRY2 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:1591 | renovascular hypertension | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:10286 | prostate carcinoma | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:2377 | multiple sclerosis | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:7148 | rheumatoid arthritis | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:11054 | urinary bladder cancer | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:3627 | aortic aneurysm | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:182 | calcinosis | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:640 | encephalomyelitis | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:4247 | coronary restenosis | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:0111535 | progressive osseous heteroplasia | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:1793 | pancreatic cancer | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:4306 | radiculopathy | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:14566 | disease of cellular proliferation | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:11832 | visual epilepsy | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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| DOID:5844 | myocardial infarction | HGNC:11255 | Homo sapiens (human) | 6696 | SPP1 |
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