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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
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Repository for lectin-assisted multimodality data
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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:0081124 | craniofacial dysmorphism, skeletal anomalies, and impaired intellectual development syndrome 1 | HGNC:18188 | Homo sapiens (human) | 54499 | TMCO1 |
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| DOID:10155 | intestinal cancer | HGNC:18196 | Homo sapiens (human) | 83595 | SOX7 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:18196 | Homo sapiens (human) | 83595 | SOX7 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:1820 | Homo sapiens (human) | 1088 | CEACAM8 |
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| DOID:0070453 | xanthinuria type II | HGNC:18234 | Homo sapiens (human) | 55034 | MOCOS |
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| DOID:0060041 | autism spectrum disorder | HGNC:18234 | Homo sapiens (human) | 55034 | MOCOS |
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| DOID:0070314 | obstructive nephropathy | HGNC:18234 | Homo sapiens (human) | 55034 | MOCOS |
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| DOID:9408 | acute myocardial infarction | HGNC:18239 | Homo sapiens (human) | 55114 | ARHGAP17 |
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| DOID:0081220 | autosomal recessive intellectual developmental disorder 58 | HGNC:18248 | Homo sapiens (human) | 55250 | ELP2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:18248 | Homo sapiens (human) | 55250 | ELP2 |
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| DOID:1059 | intellectual disability | HGNC:18248 | Homo sapiens (human) | 55250 | ELP2 |
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| DOID:1289 | neurodegenerative disease | HGNC:18261 | Homo sapiens (human) | 55666 | NPLOC4 |
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| DOID:680 | tauopathy | HGNC:18271 | Homo sapiens (human) | 55740 | ENAH |
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| DOID:684 | hepatocellular carcinoma | HGNC:18271 | Homo sapiens (human) | 55740 | ENAH |
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||
| DOID:2841 | asthma | HGNC:18274 | Homo sapiens (human) | 57105 | CYSLTR2 |
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| DOID:4483 | rhinitis | HGNC:18274 | Homo sapiens (human) | 57105 | CYSLTR2 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:18274 | Homo sapiens (human) | 57105 | CYSLTR2 |
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| DOID:0080822 | aspirin-induced respiratory disease | HGNC:18274 | Homo sapiens (human) | 57105 | CYSLTR2 |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:18290 | Homo sapiens (human) | 55907 | CMAS |
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| DOID:6406 | double outlet right ventricle | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:0050545 | visceral heterotaxy | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:0060856 | right atrial isomerism | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
|
