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GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
UniCarb-DR
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:0111836 | congenital nongoitrous hypothyroidism 7 | HGNC:12299 | Homo sapiens (human) | 7201 | TRHR |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:0080939 | hereditary angioedema type I | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:4989 | pancreatitis | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:14115 | toxic shock syndrome | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:0080600 | COVID-19 | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:14735 | hereditary angioedema | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:3526 | cerebral infarction | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:1558 | angioedema | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:3068 | glioblastoma | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:4448 | macular degeneration | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:9408 | acute myocardial infarction | HGNC:1228 | Homo sapiens (human) | 710 | SERPING1 |
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| DOID:0060674 | catecholaminergic polymorphic ventricular tachycardia | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:12930 | dilated cardiomyopathy | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:0060679 | catecholaminergic polymorphic ventricular tachycardia 5 | HGNC:12261 | Homo sapiens (human) | 10345 | TRDN |
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| DOID:0112312 | male infertility due to globozoospermia | HGNC:12028 | Homo sapiens (human) | 7184 | HSP90B1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:12028 | Homo sapiens (human) | 7184 | HSP90B1 |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:12020 | Homo sapiens (human) | 8460 | TPST1 |
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| DOID:0060308 | autosomal recessive intellectual developmental disorder | HGNC:12017 | Homo sapiens (human) | 7175 | TPR |
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| DOID:1324 | lung cancer | HGNC:12017 | Homo sapiens (human) | 7175 | TPR |
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| DOID:612 | primary immunodeficiency disease | HGNC:12016 | Homo sapiens (human) | 7174 | TPP2 |
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| DOID:0050328 | congenital hypothyroidism | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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| DOID:0112186 | thyroid dyshormonogenesis 2A | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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| DOID:2921 | glomerulonephritis | HGNC:12015 | Homo sapiens (human) | 7173 | TPO |
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