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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:14330 | Parkinson's disease | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:0060893 | juvenile-onset Parkinson's disease | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:0060556 | Kufor-Rakeb syndrome | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:14557 | primary pulmonary hypertension | HGNC:24113 | Homo sapiens (human) | 79572 | ATP13A3 |
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| DOID:0060309 | syndromic X-linked intellectual disability | HGNC:29873 | Homo sapiens (human) | 79576 | NKAP |
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| DOID:5520 | head and neck squamous cell carcinoma | HGNC:16783 | Homo sapiens (human) | 79577 | CDC73 |
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| DOID:13543 | hyperparathyroidism | HGNC:16783 | Homo sapiens (human) | 79577 | CDC73 |
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| DOID:3910 | lung adenocarcinoma | HGNC:16783 | Homo sapiens (human) | 79577 | CDC73 |
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| DOID:1540 | parathyroid carcinoma | HGNC:16783 | Homo sapiens (human) | 79577 | CDC73 |
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| DOID:9256 | colorectal cancer | HGNC:16783 | Homo sapiens (human) | 79577 | CDC73 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:16783 | Homo sapiens (human) | 79577 | CDC73 |
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| DOID:2876 | laryngeal squamous cell carcinoma | HGNC:16783 | Homo sapiens (human) | 79577 | CDC73 |
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| DOID:0050694 | Brown-Vialetto-Van Laere syndrome | HGNC:30224 | Homo sapiens (human) | 79581 | SLC52A2 |
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| DOID:0080786 | Brown-Vialetto-Van Laere syndrome 2 | HGNC:30224 | Homo sapiens (human) | 79581 | SLC52A2 |
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| DOID:0110989 | Joubert syndrome 20 | HGNC:37234 | Homo sapiens (human) | 79583 | TMEM231 |
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| DOID:0050778 | Meckel syndrome | HGNC:37234 | Homo sapiens (human) | 79583 | TMEM231 |
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| DOID:4501 | orofaciodigital syndrome | HGNC:37234 | Homo sapiens (human) | 79583 | TMEM231 |
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| DOID:9970 | obesity | HGNC:26161 | Homo sapiens (human) | 79585 | CORO7 |
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| DOID:1682 | congenital heart disease | HGNC:29813 | Homo sapiens (human) | 79595 | SAP130 |
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| DOID:9955 | hypoplastic left heart syndrome | HGNC:29813 | Homo sapiens (human) | 79595 | SAP130 |
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| DOID:326 | ischemia | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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| DOID:11400 | pyelonephritis | HGNC:1437 | Homo sapiens (human) | 796 | CALCA |
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