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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:2861 | congenital nonspherocytic hemolytic anemia | SGD:S000005185 | Saccharomyces cerevisiae S288C | 855480 | ZWF1 |
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| DOID:5419 | schizophrenia | MGI:87986 | Mus musculus (house mouse) | 11651 | Akt1 |
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| DOID:5419 | schizophrenia | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:5419 | schizophrenia | HGNC:4617 | Homo sapiens (human) | 2932 | GSK3B |
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| DOID:3328 | temporal lobe epilepsy | HGNC:4341 | Homo sapiens (human) | 2752 | GLUL |
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| DOID:3323 | Sandhoff disease | MGI:96074 | Mus musculus (house mouse) | 15212 | Hexb |
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| DOID:10763 | hypertension | RGD:2379 | Rattus norvegicus (Norway rat) | 24267 | Comt |
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| DOID:9273 | citrullinemia | MGI:1354721 | Mus musculus (house mouse) | 50799 | Slc25a13 |
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| DOID:9743 | diabetic neuropathy | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:9744 | type 1 diabetes mellitus | MGI:96545 | Mus musculus (house mouse) | 16177 | Il1r1 |
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| DOID:0110635 | muscular dystrophy-dystroglycanopathy type B5 | HGNC:17997 | Homo sapiens (human) | 79147 | FKRP |
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| DOID:0050663 | Bethlem myopathy | MGI:88459 | Mus musculus (house mouse) | 12833 | Col6a1 |
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| DOID:9452 | steatotic liver disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:9970 | obesity | MGI:104963 | Mus musculus (house mouse) | 18166 | Npy1r |
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| DOID:2671 | transitional cell carcinoma | HGNC:9599 | Homo sapiens (human) | 9536 | PTGES |
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| DOID:0050811 | congenital adrenal hyperplasia | HGNC:2591 | Homo sapiens (human) | 1584 | CYP11B1 |
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| DOID:9970 | obesity | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:0110637 | muscular dystrophy-dystroglycanopathy type B6 | HGNC:6511 | Homo sapiens (human) | 9215 | LARGE1 |
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| DOID:9744 | type 1 diabetes mellitus | MGI:96572 | Mus musculus (house mouse) | 16333 | Ins1 |
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| DOID:9744 | type 1 diabetes mellitus | MGI:96573 | Mus musculus (house mouse) | 16334 | Ins2 |
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| DOID:4989 | pancreatitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:9266 | cystinuria | MGI:1195264 | Mus musculus (house mouse) | 20532 | Slc3a1 |
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| DOID:0050644 | arterial calcification of infancy | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:9970 | obesity | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1184 | nephrotic syndrome | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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