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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References ▼ |
|---|---|---|---|---|---|---|---|---|
| DOID:224 | transient cerebral ischemia | RGD:3269 | Rattus norvegicus (Norway rat) | 25737 | Pcna |
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| DOID:5844 | myocardial infarction | RGD:619719 | Rattus norvegicus (Norway rat) | 81829 | Mdh2 |
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| DOID:10652 | Alzheimer's disease | HGNC:612 | Homo sapiens (human) | 347 | APOD |
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| DOID:8567 | Hodgkin's lymphoma | HGNC:10658 | Homo sapiens (human) | 6382 | SDC1 |
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| DOID:2018 | hyperinsulinism | RGD:3307 | Rattus norvegicus (Norway rat) | 24638 | Pfkfb1 |
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| DOID:1612 | breast cancer | HGNC:9065 | Homo sapiens (human) | 5335 | PLCG1 |
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| DOID:0080217 | lysosomal acid lipase deficiency | MGI:96789 | Mus musculus (house mouse) | 16889 | Lipa |
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| DOID:11151 | cholecystolithiasis | HGNC:9031 | Homo sapiens (human) | 5320 | PLA2G2A |
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| DOID:3146 | lipid metabolism disorder | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:2747 | glycogen storage disease | HGNC:4707 | Homo sapiens (human) | 2998 | GYS2 |
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| DOID:655 | inherited metabolic disorder | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:1926 | Gaucher's disease | HGNC:9020 | Homo sapiens (human) | 5313 | PKLR |
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| DOID:2018 | hyperinsulinism | HGNC:6081 | Homo sapiens (human) | 3630 | INS |
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| DOID:11396 | pulmonary edema | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:3651 | pyruvate carboxylase deficiency disease | HGNC:8636 | Homo sapiens (human) | 5091 | PC |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:820 | myocarditis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:2580 | rhizomelic chondrodysplasia punctata | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:2211 | factor XIII deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:2216 | factor V deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:2747 | glycogen storage disease | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:7216 | Homo sapiens (human) | 4351 | MPI |
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| DOID:1612 | breast cancer | HGNC:9604 | Homo sapiens (human) | 5742 | PTGS1 |
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| DOID:10652 | Alzheimer's disease | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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