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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:14497 | Wolman disease | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:2741 | bilirubin metabolic disorder | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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| DOID:4947 | cholangiocarcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:19743 | Homo sapiens (human) | 29954 | POMT2 |
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| DOID:0110958 | Gaucher's disease type II | HGNC:4177 | Homo sapiens (human) | 2629 | GBA1 |
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| DOID:0111027 | hemochromatosis type 2A | HGNC:4887 | Homo sapiens (human) | 148738 | HJV |
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| DOID:0060849 | osteoporosis-pseudoglioma syndrome | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:10587 | Krabbe disease | HGNC:4115 | Homo sapiens (human) | 2581 | GALC |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:684 | hepatocellular carcinoma | HGNC:9232 | Homo sapiens (human) | 5465 | PPARA |
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| DOID:9775 | diastolic heart failure | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10652 | Alzheimer's disease | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:13628 | favism | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0080124 | mitochondrial DNA depletion syndrome 5 | HGNC:11448 | Homo sapiens (human) | 8803 | SUCLA2 |
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| DOID:0111619 | combined D-2- and L-2-hydroxyglutaric aciduria | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0110170 | Charcot-Marie-Tooth disease axonal type 2Q | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0070238 | primary coenzyme Q10 deficiency 1 | HGNC:25223 | Homo sapiens (human) | 27235 | COQ2 |
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| DOID:10763 | hypertension | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:206 | hereditary multiple exostoses | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:1612 | breast cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5993 | Homo sapiens (human) | 3554 | IL1R1 |
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