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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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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 | 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 | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:4449 | Homo sapiens (human) | 2817 | GPC1 |
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| DOID:0060248 | Simpson-Golabi-Behmel syndrome type 1 | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:684 | hepatocellular carcinoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:2154 | nephroblastoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:5082 | liver cirrhosis | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:2129 | atypical teratoid rhabdoid tumor | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:3596 | placental site trophoblastic tumor | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:687 | hepatoblastoma | HGNC:4451 | Homo sapiens (human) | 2719 | GPC3 |
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| DOID:0080844 | omodysplasia 1 | HGNC:4454 | Homo sapiens (human) | 10082 | GPC6 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4456 | Homo sapiens (human) | 2820 | GPD2 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:14330 | Parkinson's disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9119 | acute myeloid leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:589 | congenital hemolytic anemia | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:440 | neuromuscular disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:114 | heart disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:1059 | intellectual disability | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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| DOID:0080932 | primary localized cutaneous amyloidosis 3 | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:3454 | brain infarction | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:0060680 | pigment dispersion syndrome | HGNC:4462 | Homo sapiens (human) | 10457 | GPNMB |
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| DOID:11054 | urinary bladder cancer | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:3459 | breast carcinoma | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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| DOID:0060602 | alpha-methylacyl-CoA racemase deficiency | HGNC:451 | Homo sapiens (human) | 23600 | AMACR |
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