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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:0050450 | Gitelman syndrome | HGNC:10912 | Homo sapiens (human) | 6559 | SLC12A3 |
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| DOID:10003 | sensorineural hearing loss | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:11832 | visual epilepsy | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:224 | transient cerebral ischemia | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:0112159 | autosomal dominant nonsyndromic deafness 78 | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:10763 | hypertension | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:1826 | epilepsy | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:445 | Bartter disease | HGNC:10910 | Homo sapiens (human) | 6557 | SLC12A1 |
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| DOID:0110142 | Bartter disease type 1 | HGNC:10910 | Homo sapiens (human) | 6557 | SLC12A1 |
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| DOID:1826 | epilepsy | HGNC:10910 | Homo sapiens (human) | 6557 | SLC12A1 |
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| DOID:0111028 | hemochromatosis type 4 | HGNC:10909 | Homo sapiens (human) | 30061 | SLC40A1 |
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| DOID:11758 | iron deficiency anemia | HGNC:10909 | Homo sapiens (human) | 30061 | SLC40A1 |
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| DOID:14330 | Parkinson's disease | HGNC:10909 | Homo sapiens (human) | 30061 | SLC40A1 |
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| DOID:14330 | Parkinson's disease | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:552 | pneumonia | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:1724 | duodenal ulcer | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:0050425 | restless legs syndrome | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:0080855 | Parkinsonism | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:11759 | hypochromic anemia | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:2316 | brain ischemia | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:11758 | iron deficiency anemia | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:2355 | anemia | HGNC:10908 | Homo sapiens (human) | 4891 | SLC11A2 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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