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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:9120 | amyloidosis | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:0050700 | cardiomyopathy | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:224 | transient cerebral ischemia | HGNC:4432 | Homo sapiens (human) | 2805 | GOT1 |
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| DOID:0111402 | mucopolysaccharidosis type IIID | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:12801 | mucopolysaccharidosis III | HGNC:4422 | Homo sapiens (human) | 2799 | GNS |
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| DOID:3343 | glycoproteinosis | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:0080678 | mucolipidosis III gamma | HGNC:23026 | Homo sapiens (human) | 84572 | GNPTG |
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| DOID:0080070 | mucolipidosis II alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080071 | mucolipidosis III alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080488 | mucolipidosis | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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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:150 | disease of mental health | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| DOID:0110852 | rhizomelic chondrodysplasia punctata type 2 | HGNC:4416 | Homo sapiens (human) | 8443 | GNPAT |
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| 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:3659 | sialuria | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0080718 | GNE myopathy | HGNC:23657 | Homo sapiens (human) | 10020 | GNE |
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| DOID:0112374 | muscular dystrophy-dystroglycanopathy | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0111233 | congenital muscular dystrophy-dystroglycanopathy A14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0112377 | muscular dystrophy-dystroglycanopathy type B14 | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0110294 | autosomal recessive limb-girdle muscular dystrophy type 2T | HGNC:22932 | Homo sapiens (human) | 29925 | GMPPB |
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| DOID:0112321 | alacrima, achalasia, and impaired intellectual development syndrome | HGNC:22923 | Homo sapiens (human) | 29926 | GMPPA |
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| DOID:1067 | open-angle glaucoma | HGNC:4369 | Homo sapiens (human) | 2762 | GMDS |
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