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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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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:13366 | Stiff-Person syndrome | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:0090031 | D-bifunctional protein deficiency | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:9970 | obesity | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:10652 | Alzheimer's disease | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:9970 | obesity | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:1923 | disorder of sexual development | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:0112248 | 17-beta hydroxysteroid dehydrogenase 3 deficiency | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5212 | Homo sapiens (human) | 3293 | HSD17B3 |
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| DOID:3008 | invasive ductal carcinoma | HGNC:5210 | Homo sapiens (human) | 3292 | HSD17B1 |
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| DOID:4367 | apparent mineralocorticoid excess syndrome | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:10763 | hypertension | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:9970 | obesity | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:5844 | myocardial infarction | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:655 | inherited metabolic disorder | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:5199 | ureteral obstruction | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:0050696 | fetal alcohol spectrum disorder | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:9970 | obesity | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0090140 | cortisone reductase deficiency 2 | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10825 | essential hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:3393 | coronary artery disease | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10763 | hypertension | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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