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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
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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:13580 | cholestasis | HGNC:2651 | Homo sapiens (human) | 1581 | CYP7A1 |
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| DOID:12351 | alcoholic hepatitis | HGNC:2651 | Homo sapiens (human) | 1581 | CYP7A1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2651 | Homo sapiens (human) | 1581 | CYP7A1 |
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| DOID:13619 | extrahepatic cholestasis | HGNC:2653 | Homo sapiens (human) | 1582 | CYP8B1 |
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| DOID:10787 | premature menopause | HGNC:2653 | Homo sapiens (human) | 1582 | CYP8B1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:2653 | Homo sapiens (human) | 1582 | CYP8B1 |
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| DOID:1824 | status epilepticus | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:1924 | hypogonadism | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:10763 | hypertension | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0050546 | congenital adrenal insufficiency | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:4195 | hyperglycemia | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:2527 | nephrosis | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:11446 | sciatic neuropathy | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2590 | Homo sapiens (human) | 1583 | CYP11A1 |
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| DOID:0060732 | chromosome 9p deletion syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:0090001 | Fraser syndrome | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:23399 | Homo sapiens (human) | 158326 | FREM1 |
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| DOID:3454 | brain infarction | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:10763 | hypertension | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:446 | primary hyperaldosteronism | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:0050891 | adrenal cortical adenoma | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:114 | heart disease | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:5844 | myocardial infarction | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:820 | myocarditis | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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