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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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MIRAGE
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:4971 | myelofibrosis | HGNC:7217 | Homo sapiens (human) | 4352 | MPL |
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| DOID:0050787 | juvenile polyposis syndrome | HGNC:6770 | Homo sapiens (human) | 4089 | SMAD4 |
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| DOID:10763 | hypertension | HGNC:1029 | Homo sapiens (human) | 623 | BDKRB1 |
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| DOID:0110534 | autosomal recessive nonsyndromic deafness 89 | HGNC:6215 | Homo sapiens (human) | 3735 | KARS1 |
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| DOID:0060647 | fetal encasement syndrome | HGNC:1974 | Homo sapiens (human) | 1147 | CHUK |
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| DOID:1838 | Menkes disease | HGNC:869 | Homo sapiens (human) | 538 | ATP7A |
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| DOID:0110480 | autosomal recessive nonsyndromic deafness 22 | HGNC:16378 | Homo sapiens (human) | 146183 | OTOA |
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| DOID:0111089 | Fanconi anemia complementation group D1 | HGNC:1101 | Homo sapiens (human) | 675 | BRCA2 |
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| DOID:3770 | pulmonary fibrosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:417 | Homo sapiens (human) | 229 | ALDOB |
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| DOID:0050632 | oculocutaneous albinism | HGNC:12442 | Homo sapiens (human) | 7299 | TYR |
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| DOID:10763 | hypertension | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050947 | hereditary hypophosphatemic rickets with hypercalciuria | HGNC:11019 | Homo sapiens (human) | 6569 | SLC34A1 |
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| DOID:0060439 | lysinuric protein intolerance | HGNC:11065 | Homo sapiens (human) | 9056 | SLC7A7 |
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| DOID:0080109 | infantile myofibromatosis | HGNC:8804 | Homo sapiens (human) | 5159 | PDGFRB |
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| DOID:0090125 | brain small vessel disease 1 | HGNC:2202 | Homo sapiens (human) | 1282 | COL4A1 |
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| DOID:0080181 | PHARC syndrome | HGNC:15868 | Homo sapiens (human) | 26090 | ABHD12 |
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| DOID:12120 | pulmonary alveolar proteinosis | HGNC:33 | Homo sapiens (human) | 21 | ABCA3 |
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| DOID:0110154 | Charcot-Marie-Tooth disease type 2A1 | HGNC:16636 | Homo sapiens (human) | 23095 | KIF1B |
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| DOID:0050633 | ocular albinism 1 | HGNC:20145 | Homo sapiens (human) | 4935 | GPR143 |
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| DOID:10629 | microphthalmia | HGNC:4837 | Homo sapiens (human) | 3052 | HCCS |
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| DOID:576 | proteinuria | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0111100 | maturity-onset diabetes of the young type 2 | HGNC:4195 | Homo sapiens (human) | 2645 | GCK |
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| DOID:3627 | aortic aneurysm | HGNC:3219 | Homo sapiens (human) | 30008 | EFEMP2 |
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| DOID:0080021 | Schmid metaphyseal chondrodysplasia | HGNC:2185 | Homo sapiens (human) | 1300 | COL10A1 |
|
