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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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:0050570 | congenital disorder of glycosylation type I | HGNC:20266 | Homo sapiens (human) | 29880 | ALG5 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000006148 | Saccharomyces cerevisiae S288C | 855874 | ALG5 |
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| DOID:0080556 | congenital disorder of glycosylation Id | SGD:S000000178 | Saccharomyces cerevisiae S288C | 852196 | ALG3 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:5212 | congenital disorder of glycosylation | SGD:S000000178 | Saccharomyces cerevisiae S288C | 852196 | ALG3 |
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| DOID:0080556 | congenital disorder of glycosylation Id | HGNC:23056 | Homo sapiens (human) | 10195 | ALG3 |
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| DOID:0080561 | congenital disorder of glycosylation Ii | SGD:S000003033 | Saccharomyces cerevisiae S288C | 852815 | ALG2 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | SGD:S000003033 | Saccharomyces cerevisiae S288C | 852815 | ALG2 |
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| DOID:0080561 | congenital disorder of glycosylation Ii | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0110669 | congenital myasthenic syndrome 14 | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0080563 | congenital disorder of glycosylation Ik | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:37258 | Homo sapiens (human) | 644974 | ALG1L2 |
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| DOID:0110658 | congenital myasthenic syndrome 15 | SGD:S000000274 | Saccharomyces cerevisiae S288C | 852362 | ALG14 |
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| DOID:0110658 | congenital myasthenic syndrome 15 | HGNC:28287 | Homo sapiens (human) | 199857 | ALG14 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | SGD:S000003015 | Saccharomyces cerevisiae S288C | 852835 | ALG13 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | HGNC:30881 | Homo sapiens (human) | 79868 | ALG13 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | SGD:S000005313 | Saccharomyces cerevisiae S288C | 855764 | ALG12 |
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| DOID:0080559 | congenital disorder of glycosylation Ig | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005313 | Saccharomyces cerevisiae S288C | 855764 | ALG12 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:19358 | Homo sapiens (human) | 79087 | ALG12 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | SGD:S000004993 | Saccharomyces cerevisiae S288C | 855679 | ALG11 |
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| DOID:0080567 | congenital disorder of glycosylation Ip | HGNC:32456 | Homo sapiens (human) | 440138 | ALG11 |
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| DOID:0110645 | long QT syndrome 2 | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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| DOID:0050563 | nonsyndromic deafness | HGNC:31088 | Homo sapiens (human) | 144245 | ALG10B |
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