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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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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:10763 | hypertension | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:2256 | osteochondrodysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0060770 | dextro-looped transposition of the great arteries | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:3407 | carotid artery disease | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:4195 | hyperglycemia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:13481 | thanatophoric dysplasia | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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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: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:5215 | Homo sapiens (human) | 51478 | HSD17B7 |
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| DOID:1701 | steroid inherited metabolic disorder | HGNC:5215 | Homo sapiens (human) | 51478 | HSD17B7 |
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| DOID:3146 | lipid metabolism disorder | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:0050857 | Perrault syndrome | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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| DOID:10763 | hypertension | HGNC:5213 | Homo sapiens (human) | 3295 | HSD17B4 |
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