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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:0080158 | herpes simplex virus keratitis | MGI:96824 | Mus musculus (house mouse) | 21898 | Tlr4 |
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| DOID:0080158 | herpes simplex virus keratitis | FB:FBgn0262473 | Drosophila melanogaster (fruit fly) | 43222 | Tl |
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| DOID:0080158 | herpes simplex virus keratitis | RGD:621159 | Rattus norvegicus (Norway rat) | 60582 | Il1rn |
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| DOID:0080158 | herpes simplex virus keratitis | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0080158 | herpes simplex virus keratitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0080156 | X-linked adrenal hypoplasia congenita | HGNC:7960 | Homo sapiens (human) | 190 | NR0B1 |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | RGD:2014 | Rattus norvegicus (Norway rat) | 25363 | Acadvl |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | MGI:895149 | Mus musculus (house mouse) | 11370 | Acadvl |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | RGD:2011 | Rattus norvegicus (Norway rat) | 25287 | Acadl |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | MGI:87868 | Mus musculus (house mouse) | 11409 | Acads |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | RGD:620514 | Rattus norvegicus (Norway rat) | 64304 | Acads |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | MGI:87867 | Mus musculus (house mouse) | 11364 | Acadm |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | RGD:2012 | Rattus norvegicus (Norway rat) | 24158 | Acadm |
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| DOID:0080144 | childhood acute lymphocytic leukemia | HGNC:13723 | Homo sapiens (human) | 10664 | CTCF |
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| DOID:0080143 | congenital fibrosis of the extraocular muscles | MGI:107813 | Mus musculus (house mouse) | 22152 | Tubb3 |
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| DOID:0080143 | congenital fibrosis of the extraocular muscles | HGNC:19349 | Homo sapiens (human) | 55605 | KIF21A |
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| DOID:0080143 | congenital fibrosis of the extraocular muscles | HGNC:20772 | Homo sapiens (human) | 10381 | TUBB3 |
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| DOID:0080143 | congenital fibrosis of the extraocular muscles | MGI:109188 | Mus musculus (house mouse) | 16564 | Kif21a |
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| DOID:0080142 | mosaic variegated aneuploidy syndrome 2 | HGNC:30794 | Homo sapiens (human) | 9702 | CEP57 |
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| DOID:0080141 | mosaic variegated aneuploidy syndrome 1 | HGNC:1149 | Homo sapiens (human) | 701 | BUB1B |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | WB:WBGene00008918 | Caenorhabditis elegans | 179519 | pigt-1 |
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