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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:4450 | renal cell carcinoma | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:12894 | Sjogren's syndrome | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:1686 | glaucoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:12849 | autistic disorder | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:12894 | Sjogren's syndrome | HGNC:10721 | Homo sapiens (human) | 6403 | SELP |
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| DOID:14330 | Parkinson's disease | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:399 | tuberculosis | HGNC:18788 | Homo sapiens (human) | 22914 | KLRK1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9387 | Homo sapiens (human) | 53632 | PRKAG3 |
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| DOID:12217 | Lewy body dementia | HGNC:543 | Homo sapiens (human) | 308 | ANXA5 |
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| DOID:0110861 | autosomal recessive polycystic kidney disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2018 | hyperinsulinism | HGNC:4241 | Homo sapiens (human) | 2673 | GFPT1 |
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| DOID:2355 | anemia | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:0080322 | polycystic kidney disease | HGNC:9009 | Homo sapiens (human) | 5311 | PKD2 |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:14018 | alcoholic liver cirrhosis | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0110913 | adult hypophosphatasia | HGNC:438 | Homo sapiens (human) | 249 | ALPL |
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| DOID:6000 | congestive heart failure | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:9477 | pulmonary embolism | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:14330 | Parkinson's disease | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:0050424 | familial adenomatous polyposis | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:127 | leiomyoma | HGNC:270 | Homo sapiens (human) | 142 | PARP1 |
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| DOID:13378 | Kawasaki disease | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10325 | silicosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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