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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:0050453 | lissencephaly | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:11832 | visual epilepsy | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:1508 | candidiasis | ZFIN:ZDB-GENE-050309-15 | Danio rerio (zebrafish) | 503885 | fut9d |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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| DOID:9970 | obesity | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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| DOID:1826 | epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0080768 | pyridoxine-dependent epilepsy | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0080572 | congenital disorder of glycosylation Iw | RGD:1565793 | Rattus norvegicus (Norway rat) | 500972 | Stt3a |
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| DOID:331 | central nervous system disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0111442 | optic atrophy 9 | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:14330 | Parkinson's disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:1289 | neurodegenerative disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0050883 | infantile cerebellar-retinal degeneration | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:1891 | optic nerve disease | HGNC:118 | Homo sapiens (human) | 50 | ACO2 |
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| DOID:0081097 | Rafiq syndrome | RGD:1563595 | Rattus norvegicus (Norway rat) | 499751 | Man1b1 |
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| DOID:4752 | multiple system atrophy | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:0050730 | coenzyme Q10 deficiency disease | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:1184 | nephrotic syndrome | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:10603 | glucose intolerance | RGD:1306722 | Rattus norvegicus (Norway rat) | 498332 | Coq2 |
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| DOID:2394 | ovarian cancer | HGNC:8143 | Homo sapiens (human) | 4978 | OPCML |
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