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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:784 | chronic kidney disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:9452 | steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:10787 | premature menopause | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:4194 | glucose metabolism disease | HGNC:2849 | Homo sapiens (human) | 1606 | DGKA |
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| DOID:4194 | glucose metabolism disease | HGNC:2850 | Homo sapiens (human) | 1607 | DGKB |
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| DOID:0050561 | Lennox-Gastaut syndrome | HGNC:2851 | Homo sapiens (human) | 8527 | DGKD |
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| DOID:0080388 | nephrotic syndrome type 7 | HGNC:2852 | Homo sapiens (human) | 8526 | DGKE |
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| DOID:4194 | glucose metabolism disease | HGNC:2853 | Homo sapiens (human) | 1608 | DGKG |
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| DOID:3146 | lipid metabolism disorder | HGNC:2859 | Homo sapiens (human) | 1718 | DHCR24 |
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| DOID:14692 | Smith-Lemli-Opitz syndrome | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:13241 | Behcet's disease | HGNC:2860 | Homo sapiens (human) | 1717 | DHCR7 |
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| DOID:162 | cancer | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0110352 | retinitis pigmentosa 59 | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0080473 | developmental delay and seizures with or without movement abnormalities | HGNC:20603 | Homo sapiens (human) | 79947 | DHDDS |
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| DOID:0111453 | 2-aminoadipic 2-oxoadipic aciduria | HGNC:23537 | Homo sapiens (human) | 55526 | DHTKD1 |
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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:0050563 | nonsyndromic deafness | SGD:S000003459 | Saccharomyces cerevisiae S288C | 853142 | DIE2 |
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| DOID:0110645 | long QT syndrome 2 | SGD:S000003459 | Saccharomyces cerevisiae S288C | 853142 | DIE2 |
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| DOID:3650 | lactic acidosis | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:2896 | Homo sapiens (human) | 1737 | DLAT |
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| DOID:9269 | maple syrup urine disease | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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| DOID:0014667 | disease of metabolism | HGNC:2898 | Homo sapiens (human) | 1738 | DLD |
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| DOID:0050773 | paraganglioma | HGNC:2911 | Homo sapiens (human) | 1743 | DLST |
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| DOID:10652 | Alzheimer's disease | HGNC:2911 | Homo sapiens (human) | 1743 | DLST |
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