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GlyTouCan
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:0050563 | nonsyndromic deafness | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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| DOID:0050563 | nonsyndromic deafness | HGNC:23162 | Homo sapiens (human) | 84920 | ALG10 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:5212 | congenital disorder of glycosylation | SGD:S000000314 | Saccharomyces cerevisiae S288C | 852407 | ALG1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | SGD:S000000314 | Saccharomyces cerevisiae S288C | 852407 | ALG1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000000314 | Saccharomyces cerevisiae S288C | 852407 | ALG1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:418 | Homo sapiens (human) | 230 | ALDOC |
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| DOID:5154 | borna disease | HGNC:418 | Homo sapiens (human) | 230 | ALDOC |
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| DOID:438 | autoimmune disease of the nervous system | HGNC:418 | Homo sapiens (human) | 230 | ALDOC |
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| DOID:9869 | hereditary fructose intolerance syndrome | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:916 | liver benign neoplasm | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:8283 | peritonitis | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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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:1826 | epilepsy | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:411 | Homo sapiens (human) | 222 | ALDH3B2 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:410 | Homo sapiens (human) | 221 | ALDH3B1 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:403 | Homo sapiens (human) | 224 | ALDH3A2 |
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| DOID:14501 | Sjogren-Larsson syndrome | HGNC:405 | Homo sapiens (human) | 218 | ALDH3A1 |
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