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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:1064 | cystinosis | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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| DOID:1062 | Fanconi syndrome | HGNC:2518 | Homo sapiens (human) | 1497 | CTNS |
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| DOID:2977 | primary hyperoxaluria | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:0111672 | primary hyperoxaluria type 3 | HGNC:25155 | Homo sapiens (human) | 112817 | HOGA1 |
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| DOID:1793 | pancreatic cancer | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:0050741 | alcohol dependence | HGNC:251 | Homo sapiens (human) | 126 | ADH1C |
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| DOID:0110515 | autosomal recessive nonsyndromic deafness 63 | HGNC:25033 | Homo sapiens (human) | 220074 | LRTOMT |
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| DOID:0050741 | alcohol dependence | HGNC:250 | Homo sapiens (human) | 125 | ADH1B |
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| DOID:0111420 | familial GPIHBP1 deficiency | HGNC:24945 | Homo sapiens (human) | 338328 | GPIHBP1 |
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| DOID:1184 | nephrotic syndrome | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:9970 | obesity | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:10652 | Alzheimer's disease | HGNC:24864 | Homo sapiens (human) | 26330 | GAPDHS |
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| DOID:0070254 | congenital disorder of glycosylation type IIb | HGNC:24862 | Homo sapiens (human) | 7841 | MOGS |
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| DOID:0112136 | severe congenital neutropenia 4 | HGNC:24861 | Homo sapiens (human) | 92579 | G6PC3 |
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| DOID:0050753 | cerebellar ataxia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:1432 | blindness | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:1289 | neurodegenerative disease | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:24768 | Homo sapiens (human) | 375775 | PNPLA7 |
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| DOID:11725 | Cornelia de Lange syndrome | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:1059 | intellectual disability | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:0080507 | Cornelia de Lange syndrome 3 | HGNC:2468 | Homo sapiens (human) | 9126 | SMC3 |
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| DOID:2316 | brain ischemia | HGNC:2466 | Homo sapiens (human) | 1464 | CSPG4 |
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