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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:0090005 | Schwartz-Jampel syndrome 1 | HGNC:5273 | Homo sapiens (human) | 3339 | HSPG2 |
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| DOID:0081133 | 3-methylglutaconic aciduria type 7a | SGD:S000003949 | Saccharomyces cerevisiae S288C | 850633 | HSP104 |
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| DOID:0081134 | 3-methylglutaconic aciduria type 7b | SGD:S000003949 | Saccharomyces cerevisiae S288C | 850633 | HSP104 |
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| DOID:0050590 | severe congenital neutropenia | SGD:S000003949 | Saccharomyces cerevisiae S288C | 850633 | HSP104 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0111071 | congenital bile acid synthesis defect 1 | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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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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| 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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