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GlyTouCan
Glycan Structure Repository
GlyComb
Glycoconjugate Repository
GlycoPOST
Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3717 | gastric adenocarcinoma | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:8466 | retinal degeneration | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:1387 | hypolipoproteinemia | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:0060656 | autosomal recessive congenital ichthyosis 1 | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:3393 | coronary artery disease | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:9452 | steatotic liver disease | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:10230 | aortic atherosclerosis | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:0110015 | age related macular degeneration 2 | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:8501 | fundus dystrophy | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:10976 | membranous glomerulonephritis | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:4448 | macular degeneration | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:684 | hepatocellular carcinoma | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:0050817 | Stargardt disease | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:10584 | retinitis pigmentosa | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:10787 | premature menopause | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:0060712 | autosomal recessive congenital ichthyosis 4A | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:0080957 | primary hypoalphalipoproteinemia 1 | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:0060713 | autosomal recessive congenital ichthyosis 4B | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:9352 | type 2 diabetes mellitus | WB:WBGene00000020 | Caenorhabditis elegans | 171782 | abt-2 |
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| DOID:12387 | nephrogenic diabetes insipidus | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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| DOID:14219 | renal tubular acidosis | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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| DOID:11716 | prediabetes syndrome | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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| DOID:10763 | hypertension | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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| DOID:2355 | anemia | WB:WBGene00009920 | Caenorhabditis elegans | 172613 | abts-1 |
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