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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:9970 | obesity | HGNC:833 | Homo sapiens (human) | 509 | ATP5F1C |
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| DOID:5419 | schizophrenia | HGNC:833 | Homo sapiens (human) | 509 | ATP5F1C |
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| DOID:9970 | obesity | HGNC:830 | Homo sapiens (human) | 506 | ATP5F1B |
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| DOID:0050700 | cardiomyopathy | HGNC:830 | Homo sapiens (human) | 506 | ATP5F1B |
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| DOID:224 | transient cerebral ischemia | HGNC:830 | Homo sapiens (human) | 506 | ATP5F1B |
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| DOID:11612 | polycystic ovary syndrome | HGNC:830 | Homo sapiens (human) | 506 | ATP5F1B |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:830 | Homo sapiens (human) | 506 | ATP5F1B |
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| DOID:6432 | pulmonary hypertension | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:10652 | Alzheimer's disease | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:0111498 | combined oxidative phosphorylation deficiency 22 | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:0070461 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4A | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:10763 | hypertension | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:8725 | vascular dementia | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:0070462 | mitochondrial complex V (ATP synthase) deficiency nuclear type 4B | HGNC:823 | Homo sapiens (human) | 498 | ATP5F1A |
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| DOID:10534 | stomach cancer | HGNC:820 | Homo sapiens (human) | 496 | ATP4B |
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| DOID:8929 | atrophic gastritis | HGNC:820 | Homo sapiens (human) | 496 | ATP4B |
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| DOID:1826 | epilepsy | HGNC:820 | Homo sapiens (human) | 496 | ATP4B |
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| DOID:9970 | obesity | HGNC:820 | Homo sapiens (human) | 496 | ATP4B |
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| DOID:0040090 | autoimmune gastritis | HGNC:820 | Homo sapiens (human) | 496 | ATP4B |
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| DOID:0050429 | Hailey-Hailey disease | HGNC:817 | Homo sapiens (human) | 493 | ATP2B4 |
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| DOID:543 | dystonia | HGNC:817 | Homo sapiens (human) | 493 | ATP2B4 |
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| DOID:10591 | pre-eclampsia | HGNC:817 | Homo sapiens (human) | 493 | ATP2B4 |
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| DOID:11714 | gestational diabetes | HGNC:817 | Homo sapiens (human) | 493 | ATP2B4 |
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| DOID:114 | heart disease | HGNC:813 | Homo sapiens (human) | 489 | ATP2A3 |
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