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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:14330 | Parkinson's disease | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:8552 | chronic myeloid leukemia | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:8805 | intermediate coronary syndrome | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:3312 | bipolar disorder | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:893 | Wilson disease | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:0070111 | Niemann-Pick disease type A | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:14504 | Niemann-Pick disease | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:0070112 | Niemann-Pick disease type B | MGI:98325 | Mus musculus (house mouse) | 20597 | Smpd1 |
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| DOID:9266 | cystinuria | MGI:1195264 | Mus musculus (house mouse) | 20532 | Slc3a1 |
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| DOID:3393 | coronary artery disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:13810 | familial hypercholesterolemia | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:3526 | cerebral infarction | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:6432 | pulmonary hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:10763 | hypertension | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:14330 | Parkinson's disease | HGNC:3402 | Homo sapiens (human) | 2053 | EPHX2 |
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| DOID:0060470 | salt and pepper syndrome | MGI:1339963 | Mus musculus (house mouse) | 20454 | St3gal5 |
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| DOID:0050589 | inflammatory bowel disease | MGI:1341826 | Mus musculus (house mouse) | 20445 | St6galnac1 |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | MGI:1316659 | Mus musculus (house mouse) | 20441 | St3gal3 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | MGI:1316659 | Mus musculus (house mouse) | 20441 | St3gal3 |
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| DOID:3070 | high grade glioma | MGI:108470 | Mus musculus (house mouse) | 20440 | St6gal1 |
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| DOID:1574 | alcohol use disorder | MGI:108470 | Mus musculus (house mouse) | 20440 | St6gal1 |
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| DOID:0060718 | autosomal recessive congenital ichthyosis 9 | HGNC:23752 | Homo sapiens (human) | 204219 | CERS3 |
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| DOID:0081376 | obsolete sorbitol dehydrogenase deficiency with peripheral neuropathy | MGI:98266 | Mus musculus (house mouse) | 20322 | Sord |
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