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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:0112035 | non-syndromic X-linked intellectual disability 96 | HGNC:11506 | Homo sapiens (human) | 6855 | SYP |
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| DOID:1574 | alcohol use disorder | HGNC:11506 | Homo sapiens (human) | 6855 | SYP |
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| DOID:10652 | Alzheimer's disease | HGNC:11506 | Homo sapiens (human) | 6855 | SYP |
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| DOID:0060894 | early-onset Parkinson's disease | HGNC:11504 | Homo sapiens (human) | 8871 | SYNJ2 |
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| DOID:14250 | Down syndrome | HGNC:11504 | Homo sapiens (human) | 8871 | SYNJ2 |
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| DOID:14330 | Parkinson's disease | HGNC:11504 | Homo sapiens (human) | 8871 | SYNJ2 |
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| DOID:14250 | Down syndrome | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0060898 | Parkinson's disease 20 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0060894 | early-onset Parkinson's disease | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:14330 | Parkinson's disease | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0080464 | developmental and epileptic encephalopathy 53 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:5419 | schizophrenia | HGNC:11497 | Homo sapiens (human) | 8831 | SYNGAP1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11497 | Homo sapiens (human) | 8831 | SYNGAP1 |
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| DOID:0070035 | autosomal dominant intellectual developmental disorder 5 | HGNC:11497 | Homo sapiens (human) | 8831 | SYNGAP1 |
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| DOID:0060037 | developmental disorder of mental health | HGNC:11497 | Homo sapiens (human) | 8831 | SYNGAP1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11496 | Homo sapiens (human) | 8224 | SYN3 |
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| DOID:1826 | epilepsy | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:5419 | schizophrenia | HGNC:11495 | Homo sapiens (human) | 6854 | SYN2 |
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| DOID:0060041 | autism spectrum disorder | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:1470 | major depressive disorder | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:0112122 | X-linked epilepsy with variable learning disabilities and behavior disorders | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:0112029 | non-syndromic X-linked intellectual disability 50 | HGNC:11494 | Homo sapiens (human) | 6853 | SYN1 |
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| DOID:4780 | anti-basement membrane glomerulonephritis | HGNC:11491 | Homo sapiens (human) | 6850 | SYK |
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| DOID:612 | primary immunodeficiency disease | HGNC:11491 | Homo sapiens (human) | 6850 | SYK |
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