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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:0111843 | Paganini-Miozzo syndrome | HGNC:19133 | Homo sapiens (human) | 90161 | HS6ST2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:18129 | Homo sapiens (human) | 51738 | GHRL |
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| DOID:0110736 | neurodegeneration with brain iron accumulation 2b | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:1192 | peripheral nervous system neoplasm | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0080600 | COVID-19 | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1700 | X-linked ichthyosis | HGNC:11425 | Homo sapiens (human) | 412 | STS |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0110409 | retinitis pigmentosa 46 | HGNC:5385 | Homo sapiens (human) | 3420 | IDH3B |
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| DOID:9351 | diabetes mellitus | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0002116 | pterygium | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0111070 | congenital bile acid synthesis defect 3 | HGNC:2652 | Homo sapiens (human) | 9420 | CYP7B1 |
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| DOID:4948 | gallbladder carcinoma | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:10825 | essential hypertension | HGNC:10522 | Homo sapiens (human) | 6296 | ACSM3 |
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| DOID:0112218 | developmental and epileptic encephalopathy 83 | HGNC:12527 | Homo sapiens (human) | 7360 | UGP2 |
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| DOID:0111451 | progressive myoclonus epilepsy 8 | HGNC:14253 | Homo sapiens (human) | 10715 | CERS1 |
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| DOID:10887 | lepromatous leprosy | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:4450 | renal cell carcinoma | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:3659 | sialuria | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0050742 | nicotine dependence | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:0111390 | mucopolysaccharidosis Ih | HGNC:5391 | Homo sapiens (human) | 3425 | IDUA |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0080564 | congenital disorder of glycosylation Il | HGNC:15672 | Homo sapiens (human) | 79796 | ALG9 |
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| DOID:10283 | prostate cancer | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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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:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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