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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:5082 | liver cirrhosis | HGNC:5987 | Homo sapiens (human) | 10068 | IL18BP |
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| DOID:1485 | cystic fibrosis | HGNC:5987 | Homo sapiens (human) | 10068 | IL18BP |
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| DOID:5844 | myocardial infarction | HGNC:5987 | Homo sapiens (human) | 10068 | IL18BP |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:5987 | Homo sapiens (human) | 10068 | IL18BP |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:5987 | Homo sapiens (human) | 10068 | IL18BP |
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| DOID:0060041 | autism spectrum disorder | HGNC:10564 | Homo sapiens (human) | 10066 | SCAMP2 |
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| DOID:6713 | cerebrovascular disease | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:3393 | coronary artery disease | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:5844 | myocardial infarction | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:5425 | ovarian hyperstimulation syndrome | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:9970 | obesity | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:3526 | cerebral infarction | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:1936 | atherosclerosis | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:13001 | carotid stenosis | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:10591 | pre-eclampsia | HGNC:7966 | Homo sapiens (human) | 10062 | NR1H3 |
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| DOID:0060569 | hypertrichotic osteochondrodysplasia Cantu type | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:0110451 | dilated cardiomyopathy 1O | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:11446 | sciatic neuropathy | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:10763 | hypertension | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:0080855 | Parkinsonism | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:0050650 | familial atrial fibrillation | HGNC:60 | Homo sapiens (human) | 10060 | ABCC9 |
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| DOID:3770 | pulmonary fibrosis | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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