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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:3525 | middle cerebral artery infarction | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0111741 | X-linked deafness 5 | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
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| DOID:0060536 | mitochondrial complex I deficiency | HGNC:8768 | Homo sapiens (human) | 9131 | AIFM1 |
|
||
| DOID:3393 | coronary artery disease | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:5844 | myocardial infarction | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:11714 | gestational diabetes | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:9970 | obesity | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
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| DOID:0080628 | alopecia-mental retardation syndrome 1 | HGNC:349 | Homo sapiens (human) | 197 | AHSG |
|
||
| DOID:0112142 | retinitis pigmentosa 85 | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:6432 | pulmonary hypertension | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:0050741 | alcohol dependence | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:12351 | alcoholic hepatitis | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:9649 | congenital nystagmus | HGNC:348 | Homo sapiens (human) | 196 | AHR |
|
||
| DOID:10763 | hypertension | HGNC:348 | Homo sapiens (human) | 196 | AHR |
|
||
| DOID:0081292 | traumatic brain injury | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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||
| DOID:1793 | pancreatic cancer | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:224 | transient cerebral ischemia | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:11984 | hypertrophic cardiomyopathy | HGNC:348 | Homo sapiens (human) | 196 | AHR |
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| DOID:417 | autoimmune disease | HGNC:347 | Homo sapiens (human) | 79026 | AHNAK |
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| DOID:0070055 | Xia-Gibbs Syndrome | HGNC:25230 | Homo sapiens (human) | 27245 | AHDC1 |
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| DOID:0111039 | hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase | HGNC:343 | Homo sapiens (human) | 191 | AHCY |
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| DOID:9452 | steatotic liver disease | HGNC:343 | Homo sapiens (human) | 191 | AHCY |
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| DOID:8455 | pyridoxine deficiency anemia | HGNC:343 | Homo sapiens (human) | 191 | AHCY |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:343 | Homo sapiens (human) | 191 | AHCY |
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