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GlyTouCan
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:0111258 | pentosuria | WB:WBGene00000984 | Caenorhabditis elegans | 179741 | dhs-21 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:0080470 | developmental and epileptic encephalopathy 36 | WB:WBGene00011193 | Caenorhabditis elegans | 179890 | algn-13 |
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| DOID:0060227 | Adams-Oliver syndrome | WB:WBGene00010386 | Caenorhabditis elegans | 179990 | H12D21.10 |
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| DOID:0060174 | GABA aminotransferase deficiency | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:10763 | hypertension | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:9976 | heroin dependence | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:11832 | visual epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0080855 | Parkinsonism | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:10652 | Alzheimer's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:2548 | reflex epilepsy | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:0050562 | West syndrome | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:12858 | Huntington's disease | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:1824 | status epilepticus | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:1596 | depressive disorder | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:326 | ischemia | HGNC:23 | Homo sapiens (human) | 18 | ABAT |
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| DOID:687 | hepatoblastoma | HGNC:3002 | Homo sapiens (human) | 1800 | DPEP1 |
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| DOID:0080488 | mucolipidosis | MGI:97305 | Mus musculus (house mouse) | 18010 | Neu1 |
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| DOID:3343 | glycoproteinosis | MGI:97305 | Mus musculus (house mouse) | 18010 | Neu1 |
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| DOID:0050579 | glycogen storage disease XV | WB:WBGene00012020 | Caenorhabditis elegans | 180119 | gyg-2 |
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| DOID:2747 | glycogen storage disease | WB:WBGene00012020 | Caenorhabditis elegans | 180119 | gyg-2 |
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| DOID:0050571 | congenital disorder of glycosylation type II | WB:WBGene00001629 | Caenorhabditis elegans | 180302 | gly-4 |
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| DOID:3211 | lysosomal storage disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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| DOID:3323 | Sandhoff disease | WB:WBGene00020509 | Caenorhabditis elegans | 180533 | hex-1 |
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