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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:684 | hepatocellular carcinoma | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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| DOID:0111037 | glycine N-methyltransferase deficiency | HGNC:4415 | Homo sapiens (human) | 27232 | GNMT |
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| DOID:12804 | mucopolysaccharidosis IV | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0080502 | GM1 gangliosidosis type 1 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0111392 | mucopolysaccharidosis type IVB | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0080501 | GM1 gangliosidosis type 2 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:3322 | GM1 gangliosidosis | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:0080489 | GM1 gangliosidosis type 3 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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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:14499 | Fabry disease | HGNC:4296 | Homo sapiens (human) | 2717 | GLA |
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| DOID:3211 | lysosomal storage disease | HGNC:4296 | Homo sapiens (human) | 2717 | GLA |
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| DOID:2841 | asthma | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:12053 | cryptococcosis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:0050127 | sinusitis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:10325 | silicosis | HGNC:17432 | Homo sapiens (human) | 27159 | CHIA |
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| DOID:0060363 | glycerol kinase deficiency | HGNC:4291 | Homo sapiens (human) | 2712 | GK2 |
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| DOID:0060363 | glycerol kinase deficiency | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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| DOID:13810 | familial hypercholesterolemia | HGNC:4289 | Homo sapiens (human) | 2710 | GK |
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| DOID:3770 | pulmonary fibrosis | HGNC:921 | Homo sapiens (human) | 27087 | B3GAT1 |
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