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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
LM-GlycoRepo
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:1935 | Bardet-Biedl syndrome | HGNC:13081 | Homo sapiens (human) | 49855 | SCAPER |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:13054 | Homo sapiens (human) | 9203 | ZMYM3 |
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| DOID:0070062 | Arboleda-Tham syndrome | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:11198 | DiGeorge syndrome | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:9119 | acute myeloid leukemia | HGNC:13013 | Homo sapiens (human) | 7994 | KAT6A |
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| DOID:13832 | patent ductus arteriosus | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:10486 | intestinal atresia | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:4977 | lymphedema | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:13099 | Moyamoya disease | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:0050827 | rheumatic heart disease | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:130 | Homo sapiens (human) | 59 | ACTA2 |
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| DOID:326 | ischemia | HGNC:12950 | Homo sapiens (human) | 7536 | SF1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12949 | Homo sapiens (human) | 7716 | VEZF1 |
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| DOID:14250 | Down syndrome | HGNC:1291 | Homo sapiens (human) | 9980 | DOP1B |
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| DOID:0080685 | aortic dissection | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0110927 | nemaline myopathy 3 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:14004 | thoracic aortic aneurysm | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081112 | Baraitser-Winter syndrome 1 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
|
||
| DOID:13832 | patent ductus arteriosus | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
|
||
| DOID:10486 | intestinal atresia | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
|
||
| DOID:13099 | Moyamoya disease | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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||
| DOID:0110550 | autosomal dominant nonsyndromic deafness 20 | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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| DOID:0081340 | congenital myopathy 2C | HGNC:129 | Homo sapiens (human) | 58 | ACTA1 |
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