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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names ▲ | References |
|---|---|---|---|---|---|---|---|---|
| DOID:4247 | coronary restenosis | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:9538 | multiple myeloma | HGNC:12441 | Homo sapiens (human) | 7298 | TYMS |
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| DOID:0110460 | dilated cardiomyopathy 2A | HGNC:11947 | Homo sapiens (human) | 7137 | TNNI3 |
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| DOID:0070235 | Loeys-Dietz syndrome 1 | HGNC:11772 | Homo sapiens (human) | 7046 | TGFBR1 |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:6001 | Homo sapiens (human) | 3558 | IL2 |
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| DOID:9155 | mucocutaneous leishmaniasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0070432 | hyperphosphatasia with impaired intellectual development syndrome 5 | HGNC:23213 | Homo sapiens (human) | 284098 | PIGW |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:5382 | Homo sapiens (human) | 3417 | IDH1 |
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| DOID:0110880 | holoprosencephaly 4 | HGNC:11776 | Homo sapiens (human) | 7050 | TGIF1 |
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| DOID:0050771 | pheochromocytoma | RGD:69062 | Rattus norvegicus (Norway rat) | 83571 | Cdkn1b |
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| DOID:219 | colon cancer | HGNC:6024 | Homo sapiens (human) | 3575 | IL7R |
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| DOID:0080527 | bronchiectasis 2 | HGNC:10599 | Homo sapiens (human) | 6337 | SCNN1A |
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| DOID:0050741 | alcohol dependence | HGNC:4600 | Homo sapiens (human) | 2918 | GRM8 |
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| DOID:8986 | narcolepsy | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:0080694 | Galloway-Mowat syndrome | HGNC:29914 | Homo sapiens (human) | 57122 | NUP107 |
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| DOID:2256 | osteochondrodysplasia | HGNC:12340 | Homo sapiens (human) | 7227 | TRPS1 |
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| DOID:3526 | cerebral infarction | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:20474 | Homo sapiens (human) | 147138 | TMC8 |
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| DOID:1070 | primary open angle glaucoma | HGNC:6665 | Homo sapiens (human) | 4016 | LOXL1 |
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| DOID:0050534 | congenital stationary night blindness | HGNC:7146 | Homo sapiens (human) | 4308 | TRPM1 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:12303 | Homo sapiens (human) | 7204 | TRIO |
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| DOID:0050650 | familial atrial fibrillation | HGNC:6242 | Homo sapiens (human) | 9992 | KCNE2 |
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| DOID:10024 | migraine with aura | HGNC:3023 | Homo sapiens (human) | 1813 | DRD2 |
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| DOID:13544 | low tension glaucoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0112035 | non-syndromic X-linked intellectual disability 96 | HGNC:11506 | Homo sapiens (human) | 6855 | SYP |
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