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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:0110777 | hereditary spastic paraplegia 26 | RGD:620490 | Rattus norvegicus (Norway rat) | 64828 | B4galnt1 |
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| DOID:10588 | adrenoleukodystrophy | HGNC:14418 | Homo sapiens (human) | 64834 | ELOVL1 |
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| DOID:162 | cancer | HGNC:19980 | Homo sapiens (human) | 64841 | GNPNAT1 |
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| DOID:0080753 | keratosis follicularis spinulosa decalvans | HGNC:19980 | Homo sapiens (human) | 64841 | GNPNAT1 |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:26125 | Homo sapiens (human) | 64847 | SPATA20 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:0080414 | developmental and epileptic encephalopathy 15 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:9970 | obesity | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:0080108 | myoglobinuria | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:3146 | lipid metabolism disorder | HGNC:14451 | Homo sapiens (human) | 64900 | LPIN3 |
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| DOID:10763 | hypertension | RGD:68396 | Rattus norvegicus (Norway rat) | 65038 | Inppl1 |
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| DOID:9970 | obesity | RGD:68396 | Rattus norvegicus (Norway rat) | 65038 | Inppl1 |
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| DOID:9352 | type 2 diabetes mellitus | RGD:68396 | Rattus norvegicus (Norway rat) | 65038 | Inppl1 |
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| DOID:0060050 | autoimmune disease of blood | RGD:621105 | Rattus norvegicus (Norway rat) | 65044 | C1galt1 |
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| DOID:5419 | schizophrenia | HGNC:18601 | Homo sapiens (human) | 65078 | RTN4R |
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| DOID:0090044 | dystonia 9 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:9351 | diabetes mellitus | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0060326 | myelomeningocele | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:10763 | hypertension | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:0090045 | childhood onset GLUT1 deficiency syndrome 2 | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:2154 | nephroblastoma | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:3525 | middle cerebral artery infarction | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:10591 | pre-eclampsia | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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| DOID:10487 | Hirschsprung's disease | HGNC:11005 | Homo sapiens (human) | 6513 | SLC2A1 |
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