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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:289 | endometriosis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:5082 | liver cirrhosis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:0111046 | platelet-type bleeding disorder 10 | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:2349 | arteriosclerosis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:5844 | myocardial infarction | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:8997 | polycythemia vera | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:10223 | dermatomyositis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:9182 | pemphigus | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:2527 | nephrosis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:3770 | pulmonary fibrosis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:10652 | Alzheimer's disease | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:2218 | blood platelet disease | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:10325 | silicosis | HGNC:1663 | Homo sapiens (human) | 948 | CD36 |
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| DOID:0112152 | CHIME syndrome | HGNC:8966 | Homo sapiens (human) | 9487 | PIGL |
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| DOID:0112216 | developmental and epileptic encephalopathy 80 | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:10112 | sleeping sickness | HGNC:8959 | Homo sapiens (human) | 9488 | PIGB |
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| DOID:10003 | sensorineural hearing loss | HGNC:1664 | Homo sapiens (human) | 949 | SCARB1 |
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| DOID:783 | end stage renal disease | HGNC:1664 | Homo sapiens (human) | 949 | SCARB1 |
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| DOID:0111399 | congenital dyserythropoietic anemia type III | HGNC:6392 | Homo sapiens (human) | 9493 | KIF23 |
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| DOID:2355 | anemia | HGNC:11033 | Homo sapiens (human) | 9497 | SLC4A7 |
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| DOID:0110839 | Usher syndrome type 2C | HGNC:11033 | Homo sapiens (human) | 9497 | SLC4A7 |
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| DOID:2355 | anemia | HGNC:11034 | Homo sapiens (human) | 9498 | SLC4A8 |
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| DOID:11716 | prediabetes syndrome | HGNC:11034 | Homo sapiens (human) | 9498 | SLC4A8 |
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