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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:10763 | hypertension | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
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| DOID:1826 | epilepsy | HGNC:799 | Homo sapiens (human) | 476 | ATP1A1 |
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| DOID:2476 | hereditary spastic paraplegia | HGNC:31789 | Homo sapiens (human) | 344905 | ATP13A5 |
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| DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:31789 | Homo sapiens (human) | 344905 | ATP13A5 |
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| DOID:0060893 | juvenile-onset Parkinson's disease | HGNC:31789 | Homo sapiens (human) | 344905 | ATP13A5 |
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| DOID:0060556 | Kufor-Rakeb syndrome | HGNC:31789 | Homo sapiens (human) | 344905 | ATP13A5 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:31789 | Homo sapiens (human) | 344905 | ATP13A5 |
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| DOID:14330 | Parkinson's disease | HGNC:31789 | Homo sapiens (human) | 344905 | ATP13A5 |
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| 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:332 | amyotrophic lateral sclerosis | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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| DOID:14503 | neuronal ceroid lipofuscinosis | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
|
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| DOID:14330 | Parkinson's disease | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
|
||
| DOID:0060893 | juvenile-onset Parkinson's disease | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
|
||
| DOID:0060556 | Kufor-Rakeb syndrome | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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||
| DOID:2476 | hereditary spastic paraplegia | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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| DOID:0112348 | hereditary spastic paraplegia 78 | HGNC:30213 | Homo sapiens (human) | 23400 | ATP13A2 |
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| DOID:0070221 | progressive familial intrahepatic cholestasis | HGNC:13543 | Homo sapiens (human) | 23120 | ATP10B |
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| DOID:0060162 | dentatorubral-pallidoluysian atrophy | HGNC:3033 | Homo sapiens (human) | 1822 | ATN1 |
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| DOID:5419 | schizophrenia | HGNC:3033 | Homo sapiens (human) | 1822 | ATN1 |
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