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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▲ |
|---|---|---|---|---|---|---|---|---|
| DOID:10611 | protein-losing enteropathy | HGNC:2665 | Homo sapiens (human) | 1604 | CD55 |
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| DOID:0111507 | Lenz-Majewski hyperostotic dwarfism | HGNC:9587 | Homo sapiens (human) | 9791 | PTDSS1 |
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| DOID:0111677 | familial benign fleck retina | HGNC:9038 | Homo sapiens (human) | 5322 | PLA2G5 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0111110 | maturity-onset diabetes of the young type 13 | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:1324 | lung cancer | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0050814 | temtamy preaxial brachydactyly syndrome | HGNC:17198 | Homo sapiens (human) | 22856 | CHSY1 |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0080265 | nephrotic syndrome type 14 | HGNC:10817 | Homo sapiens (human) | 8879 | SGPL1 |
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| DOID:0081122 | Catel Manzke syndrome | HGNC:20324 | Homo sapiens (human) | 23483 | TGDS |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10681 | Homo sapiens (human) | 6390 | SDHB |
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| DOID:1930 | Laurence-Moon syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0111458 | galactose epimerase deficiency | HGNC:4116 | Homo sapiens (human) | 2582 | GALE |
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