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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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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:10808 | gastric ulcer | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:2527 | nephrosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10159 | osteonecrosis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:5844 | myocardial infarction | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:1596 | depressive disorder | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:6543 | acne | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:9719 | neovascular inflammatory vitreoretinopathy | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:8893 | psoriasis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:874 | bacterial pneumonia | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:0070434 | hyperphosphatasia with impaired intellectual development syndrome 2 | HGNC:23215 | Homo sapiens (human) | 84720 | PIGO |
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| DOID:0080240 | non-syndromic X-linked intellectual disability 106 | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:9351 | diabetes mellitus | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:1712 | aortic valve stenosis | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:6000 | congestive heart failure | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:10741 | Homo sapiens (human) | 8482 | SEMA7A |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0111231 | congenital muscular dystrophy-dystroglycanopathy type A8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | HGNC:25904 | Homo sapiens (human) | 84899 | TMTC4 |
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| DOID:0050563 | nonsyndromic deafness | HGNC:23162 | Homo sapiens (human) | 84920 | ALG10 |
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| DOID:0070437 | hyperphosphatasia with impaired intellectual development syndrome 6 | HGNC:28213 | Homo sapiens (human) | 84992 | PIGY |
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| DOID:9452 | steatotic liver disease | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
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| DOID:0050524 | maturity-onset diabetes of the young | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
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| DOID:10763 | hypertension | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
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| DOID:4195 | hyperglycemia | SGD:S000000545 | Saccharomyces cerevisiae S288C | 850317 | GLK1 |
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