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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:7148 | rheumatoid arthritis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:10763 | hypertension | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:4448 | macular degeneration | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:10873 | Kuhnt-Junius degeneration | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:10591 | pre-eclampsia | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:2921 | glomerulonephritis | HGNC:1318 | Homo sapiens (human) | 718 | C3 |
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| DOID:0111399 | congenital dyserythropoietic anemia type III | MGI:1919069 | Mus musculus (house mouse) | 71819 | Kif23 |
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| DOID:7998 | hyperthyroidism | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:8466 | retinal degeneration | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:1459 | hypothyroidism | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:6000 | congestive heart failure | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:3312 | bipolar disorder | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:0050852 | limb ischemia | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:11984 | hypertrophic cardiomyopathy | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:12930 | dilated cardiomyopathy | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:5844 | myocardial infarction | MGI:1919082 | Mus musculus (house mouse) | 71832 | Csl |
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| DOID:0112312 | male infertility due to globozoospermia | HGNC:12028 | Homo sapiens (human) | 7184 | HSP90B1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:12028 | Homo sapiens (human) | 7184 | HSP90B1 |
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| DOID:4752 | multiple system atrophy | MGI:1919133 | Mus musculus (house mouse) | 71883 | Coq2 |
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| DOID:10603 | glucose intolerance | MGI:1919133 | Mus musculus (house mouse) | 71883 | Coq2 |
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| DOID:1184 | nephrotic syndrome | MGI:1919133 | Mus musculus (house mouse) | 71883 | Coq2 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | MGI:1919133 | Mus musculus (house mouse) | 71883 | Coq2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | MGI:1919133 | Mus musculus (house mouse) | 71883 | Coq2 |
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