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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:9970 | obesity | HGNC:14957 | Homo sapiens (human) | 9698 | PUM1 |
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||
| DOID:684 | hepatocellular carcinoma | HGNC:14946 | Homo sapiens (human) | 55607 | PPP1R9A |
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||
| DOID:12858 | Huntington's disease | HGNC:14946 | Homo sapiens (human) | 55607 | PPP1R9A |
|
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| DOID:224 | transient cerebral ischemia | HGNC:14946 | Homo sapiens (human) | 55607 | PPP1R9A |
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||
| DOID:1574 | alcohol use disorder | HGNC:14942 | Homo sapiens (human) | 79660 | PPP1R3B |
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||
| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0070382 | developmental and epileptic encephalopathy 95 | HGNC:14937 | Homo sapiens (human) | 94005 | PIGS |
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| DOID:3911 | progeria | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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||
| DOID:9970 | obesity | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:224 | transient cerebral ischemia | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14932 | Homo sapiens (human) | 23409 | SIRT4 |
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||
| DOID:11716 | prediabetes syndrome | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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||
| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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| DOID:5844 | myocardial infarction | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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||
| DOID:9352 | type 2 diabetes mellitus | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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||
| DOID:6000 | congestive heart failure | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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| DOID:10652 | Alzheimer's disease | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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| DOID:9970 | obesity | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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||
| DOID:0060611 | abdominal obesity-metabolic syndrome | HGNC:14931 | Homo sapiens (human) | 23410 | SIRT3 |
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| DOID:10907 | microcephaly | HGNC:1493 | Homo sapiens (human) | 833 | CARS1 |
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| DOID:9351 | diabetes mellitus | HGNC:14929 | Homo sapiens (human) | 23411 | SIRT1 |
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| DOID:3021 | acute kidney failure | HGNC:14929 | Homo sapiens (human) | 23411 | SIRT1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:14929 | Homo sapiens (human) | 23411 | SIRT1 |
|
