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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:2476 | hereditary spastic paraplegia | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1289 | neurodegenerative disease | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0111265 | Boucher-Neuhauser syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:3393 | coronary artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1485 | cystic fibrosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2841 | asthma | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10608 | celiac disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:552 | pneumonia | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:12236 | primary biliary cholangitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:8677 | perinatal necrotizing enterocolitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13603 | obstructive jaundice | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:11335 | sarcoidosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:1205 | allergic disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13580 | cholestasis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:13608 | biliary atresia | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:4483 | rhinitis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:10487 | Hirschsprung's disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:5844 | myocardial infarction | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:3407 | carotid artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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