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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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Repository for lectin-assisted multimodality data
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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:0070390 | developmental and epileptic encephalopathy 104 | WB:WBGene00006914 | Caenorhabditis elegans | 177626 | vha-5 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | WB:WBGene00006915 | Caenorhabditis elegans | 174743 | vha-6 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | WB:WBGene00006915 | Caenorhabditis elegans | 174743 | vha-6 |
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| DOID:14219 | renal tubular acidosis | WB:WBGene00006915 | Caenorhabditis elegans | 174743 | vha-6 |
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| DOID:0070390 | developmental and epileptic encephalopathy 104 | WB:WBGene00006915 | Caenorhabditis elegans | 174743 | vha-6 |
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| DOID:0112171 | wrinkly skin syndrome | WB:WBGene00006915 | Caenorhabditis elegans | 174743 | vha-6 |
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| DOID:0070390 | developmental and epileptic encephalopathy 104 | WB:WBGene00006916 | Caenorhabditis elegans | 178219 | vha-7 |
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| DOID:0112171 | wrinkly skin syndrome | WB:WBGene00006916 | Caenorhabditis elegans | 178219 | vha-7 |
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| DOID:0070134 | autosomal recessive cutis laxa type IIA | WB:WBGene00006916 | Caenorhabditis elegans | 178219 | vha-7 |
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| DOID:14219 | renal tubular acidosis | WB:WBGene00006916 | Caenorhabditis elegans | 178219 | vha-7 |
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| DOID:0110942 | autosomal recessive osteopetrosis 1 | WB:WBGene00006916 | Caenorhabditis elegans | 178219 | vha-7 |
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| DOID:0090125 | brain small vessel disease 1 | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:6432 | pulmonary hypertension | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:13223 | uterine fibroid | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:2921 | glomerulonephritis | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:9970 | obesity | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:0110034 | X-linked Alport syndrome | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:0111547 | retinal arterial tortuosity | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:5844 | myocardial infarction | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:0110033 | autosomal recessive Alport syndrome | FB:FBgn0016075 | Drosophila melanogaster (fruit fly) | 33726 | vkg |
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| DOID:2394 | ovarian cancer | FB:FBgn0003984 | Drosophila melanogaster (fruit fly) | 38657 | vn |
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| DOID:5844 | myocardial infarction | FB:FBgn0003984 | Drosophila melanogaster (fruit fly) | 38657 | vn |
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| DOID:2468 | psychotic disorder | FB:FBgn0003984 | Drosophila melanogaster (fruit fly) | 38657 | vn |
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| DOID:302 | substance abuse | FB:FBgn0003984 | Drosophila melanogaster (fruit fly) | 38657 | vn |
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| DOID:5419 | schizophrenia | FB:FBgn0003984 | Drosophila melanogaster (fruit fly) | 38657 | vn |
|
