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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:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:5723 | optic atrophy | HGNC:29622 | Homo sapiens (human) | 27349 | MCAT |
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| DOID:0111527 | spinal muscular atrophy with progressive myoclonic epilepsy | HGNC:735 | Homo sapiens (human) | 427 | ASAH1 |
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| DOID:0080576 | spondyloepimetaphyseal dysplasia, Genevieve-type | HGNC:19237 | Homo sapiens (human) | 54187 | NANS |
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| DOID:0080575 | Larsen-like syndrome B3GAT3 type | HGNC:923 | Homo sapiens (human) | 26229 | B3GAT3 |
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| DOID:0050636 | familial visceral amyloidosis | HGNC:6740 | Homo sapiens (human) | 4069 | LYZ |
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| DOID:10825 | essential hypertension | HGNC:2638 | Homo sapiens (human) | 1577 | CYP3A5 |
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| DOID:0080550 | Noonan syndrome with multiple lentigines 3 | HGNC:1097 | Homo sapiens (human) | 673 | BRAF |
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| DOID:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
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| DOID:0112263 | hypoinsulinemic hypoglycemia with hemihypertrophy | HGNC:392 | Homo sapiens (human) | 208 | AKT2 |
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| DOID:0070341 | neonatal-onset type II citrullinemia | HGNC:10983 | Homo sapiens (human) | 10165 | SLC25A13 |
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| DOID:0080565 | congenital disorder of glycosylation Im | HGNC:23406 | Homo sapiens (human) | 22845 | DOLK |
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| DOID:9253 | gastrointestinal stromal tumor | HGNC:10682 | Homo sapiens (human) | 6391 | SDHC |
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| DOID:0070269 | congenital disorder of glycosylation type IIq | HGNC:6546 | Homo sapiens (human) | 22796 | COG2 |
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| DOID:0080568 | congenital disorder of glycosylation Iq | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:0110435 | dilated cardiomyopathy 1GG | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:13564 | aspergillosis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:0070264 | congenital disorder of glycosylation type IIl | HGNC:18621 | Homo sapiens (human) | 57511 | COG6 |
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| DOID:0060470 | salt and pepper syndrome | HGNC:10872 | Homo sapiens (human) | 8869 | ST3GAL5 |
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| DOID:0081002 | Cowden syndrome 6 | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:2565 | macular corneal dystrophy | HGNC:6938 | Homo sapiens (human) | 4166 | CHST6 |
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| DOID:5419 | schizophrenia | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:0050635 | alternating hemiplegia of childhood | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:0111260 | phosphoribosylpyrophosphate synthetase superactivity | HGNC:9462 | Homo sapiens (human) | 5631 | PRPS1 |
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| DOID:0110741 | type 1 diabetes mellitus 2 | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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