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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:2316 | brain ischemia | SGD:S000001568 | Saccharomyces cerevisiae S288C | 853777 | MDH1 |
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| DOID:0112222 | developmental and epileptic encephalopathy 88 | HGNC:6970 | Homo sapiens (human) | 4190 | MDH1 |
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| DOID:0080433 | developmental and epileptic encephalopathy 51 | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:5844 | myocardial infarction | SGD:S000005486 | Saccharomyces cerevisiae S288C | 853994 | MDH2 |
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| DOID:0080433 | developmental and epileptic encephalopathy 51 | SGD:S000005486 | Saccharomyces cerevisiae S288C | 853994 | MDH2 |
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| DOID:2316 | brain ischemia | SGD:S000005486 | Saccharomyces cerevisiae S288C | 853994 | MDH2 |
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| DOID:6000 | congestive heart failure | SGD:S000005486 | Saccharomyces cerevisiae S288C | 853994 | MDH2 |
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| DOID:6000 | congestive heart failure | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:2316 | brain ischemia | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:5844 | myocardial infarction | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:2316 | brain ischemia | SGD:S000002236 | Saccharomyces cerevisiae S288C | 851481 | MDH3 |
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| DOID:6000 | congestive heart failure | SGD:S000002236 | Saccharomyces cerevisiae S288C | 851481 | MDH3 |
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| DOID:5844 | myocardial infarction | SGD:S000002236 | Saccharomyces cerevisiae S288C | 851481 | MDH3 |
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| DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:0111756 | Leber hereditary optic neuropathy with demyelinating disease of CNS | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:5723 | optic atrophy | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:1793 | pancreatic cancer | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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| DOID:4608 | common bile duct neoplasm | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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| DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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| DOID:0050625 | biliary tract benign neoplasm | SGD:S000004007 | Saccharomyces cerevisiae S288C | 850704 | MEU1 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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| DOID:1793 | pancreatic cancer | HGNC:7047 | Homo sapiens (human) | 11320 | MGAT4A |
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| DOID:576 | proteinuria | HGNC:7049 | Homo sapiens (human) | 4249 | MGAT5 |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:3969 | thyroid gland papillary carcinoma | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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