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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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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:0060469 | Miller-Dieker lissencephaly syndrome | MGI:894689 | Mus musculus (house mouse) | 22627 | Ywhae |
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| DOID:0060480 | left ventricular noncompaction | MGI:894689 | Mus musculus (house mouse) | 22627 | Ywhae |
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| DOID:0080282 | developmental and epileptic encephalopathy 56 | MGI:108109 | Mus musculus (house mouse) | 22628 | Ywhag |
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| DOID:11949 | Creutzfeldt-Jakob disease | MGI:108109 | Mus musculus (house mouse) | 22628 | Ywhag |
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| DOID:1059 | intellectual disability | MGI:891963 | Mus musculus (house mouse) | 22630 | Ywhaq |
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| DOID:1825 | childhood absence epilepsy | MGI:109484 | Mus musculus (house mouse) | 22631 | Ywhaz |
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| DOID:1059 | intellectual disability | MGI:109484 | Mus musculus (house mouse) | 22631 | Ywhaz |
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| DOID:684 | hepatocellular carcinoma | MGI:109484 | Mus musculus (house mouse) | 22631 | Ywhaz |
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| DOID:5419 | schizophrenia | MGI:109484 | Mus musculus (house mouse) | 22631 | Ywhaz |
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| DOID:10763 | hypertension | MGI:109484 | Mus musculus (house mouse) | 22631 | Ywhaz |
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| DOID:11832 | visual epilepsy | MGI:109484 | Mus musculus (house mouse) | 22631 | Ywhaz |
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| DOID:627 | severe combined immunodeficiency | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:0111943 | immunodeficiency 48 | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:7148 | rheumatoid arthritis | HGNC:12858 | Homo sapiens (human) | 7535 | ZAP70 |
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| DOID:0081230 | autosomal recessive intellectual developmental disorder 69 | HGNC:16740 | Homo sapiens (human) | 27107 | ZBTB11 |
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| DOID:0080201 | Peters plus syndrome | WB:WBGene00022576 | Caenorhabditis elegans | 178968 | ZC250.2 |
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| DOID:1059 | intellectual disability | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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| DOID:0081217 | autosomal recessive intellectual developmental disorder 56 | HGNC:20509 | Homo sapiens (human) | 79882 | ZC3H14 |
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| DOID:0050571 | congenital disorder of glycosylation type II | WB:WBGene00013919 | Caenorhabditis elegans | 181210 | ZC506.1 |
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| DOID:12858 | Huntington's disease | HGNC:18413 | Homo sapiens (human) | 54503 | ZDHHC13 |
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| DOID:225 | syndrome | HGNC:20342 | Homo sapiens (human) | 158866 | ZDHHC15 |
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| DOID:0050827 | rheumatic heart disease | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:9408 | acute myocardial infarction | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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