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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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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:0070049 | autosomal dominant intellectual developmental disorder 19 | HGNC:2514 | Homo sapiens (human) | 1499 | CTNNB1 |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:27424 | Homo sapiens (human) | 282996 | RBM20 |
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| DOID:612 | primary immunodeficiency disease | HGNC:18043 | Homo sapiens (human) | 55388 | MCM10 |
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| DOID:0050454 | periventricular nodular heterotopia | HGNC:15853 | Homo sapiens (human) | 10564 | ARFGEF2 |
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| DOID:13399 | color blindness | HGNC:2150 | Homo sapiens (human) | 1261 | CNGA3 |
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| DOID:12849 | autistic disorder | HGNC:4600 | Homo sapiens (human) | 2918 | GRM8 |
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| DOID:1588 | thrombocytopenia | HGNC:4036 | Homo sapiens (human) | 2533 | FYB1 |
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| DOID:2986 | IgA glomerulonephritis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:3151 | skin squamous cell carcinoma | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:3146 | lipid metabolism disorder | HGNC:7958 | Homo sapiens (human) | 4889 | NPY5R |
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| DOID:0081443 | Stolerman neurodevelopmental syndrome | HGNC:29012 | Homo sapiens (human) | 23135 | KDM6B |
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| DOID:0081046 | frontonasal dysplasia 2 | HGNC:450 | Homo sapiens (human) | 60529 | ALX4 |
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| DOID:783 | end stage renal disease | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:21350 | Homo sapiens (human) | 8050 | PDHX |
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| DOID:9970 | obesity | HGNC:8910 | Homo sapiens (human) | 5241 | PGR |
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| DOID:8893 | psoriasis | HGNC:4944 | Homo sapiens (human) | 3119 | HLA-DQB1 |
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| DOID:0111139 | mitochondrial complex III deficiency | HGNC:12587 | Homo sapiens (human) | 7386 | UQCRFS1 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:4933 | Homo sapiens (human) | 3107 | HLA-C |
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| DOID:0050591 | tooth agenesis | HGNC:13829 | Homo sapiens (human) | 80326 | WNT10A |
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| DOID:2508 | Takayasu's arteritis | HGNC:4932 | Homo sapiens (human) | 3106 | HLA-B |
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| DOID:9563 | bronchiectasis | HGNC:43 | Homo sapiens (human) | 6890 | TAP1 |
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| DOID:9976 | heroin dependence | HGNC:4083 | Homo sapiens (human) | 2562 | GABRB3 |
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| DOID:0080334 | aortic valve disease 2 | HGNC:6772 | Homo sapiens (human) | 4091 | SMAD6 |
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| DOID:2383 | neonatal jaundice | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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