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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:1924 | hypogonadism | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:1459 | hypothyroidism | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:10763 | hypertension | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:12700 | hyperprolactinemia | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:11446 | sciatic neuropathy | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:5217 | Homo sapiens (human) | 3283 | HSD3B1 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:10892 | hypospadias | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:10763 | hypertension | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:12700 | hyperprolactinemia | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:10652 | Alzheimer's disease | HGNC:5218 | Homo sapiens (human) | 3284 | HSD3B2 |
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| DOID:0111156 | spermatogenic failure 9 | FB:FBgn0030946 | Drosophila melanogaster (fruit fly) | 32854 | CG6659 |
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| DOID:14735 | hereditary angioedema | MGI:3580487 | Mus musculus (house mouse) | 328779 | Hs3st6 |
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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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| DOID:1824 | status epilepticus | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:10591 | pre-eclampsia | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:1168 | familial hyperlipidemia | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:4367 | apparent mineralocorticoid excess syndrome | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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