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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:0070376 | developmental and epileptic encephalopathy 31B | HGNC:2972 | Homo sapiens (human) | 1759 | DNM1 |
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| DOID:0070376 | developmental and epileptic encephalopathy 31B | SGD:S000001709 | Saccharomyces cerevisiae S288C | 853870 | VPS1 |
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| DOID:0070376 | developmental and epileptic encephalopathy 31B | MGI:107384 | Mus musculus (house mouse) | 13429 | Dnm1 |
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| DOID:0070374 | leukoencephalopathy with vanishing white matter 1 | HGNC:3257 | Homo sapiens (human) | 1967 | EIF2B1 |
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| DOID:0070371 | leukoencephalopathy with vanishing white matter 4 | SGD:S000003315 | Saccharomyces cerevisiae S288C | 852974 | GCD2 |
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| DOID:0070371 | leukoencephalopathy with vanishing white matter 4 | HGNC:3260 | Homo sapiens (human) | 8890 | EIF2B4 |
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| DOID:0070371 | leukoencephalopathy with vanishing white matter 4 | MGI:95300 | Mus musculus (house mouse) | 13667 | Eif2b4 |
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| DOID:0070370 | restrictive dermopathy 2 | MGI:96794 | Mus musculus (house mouse) | 16905 | Lmna |
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| DOID:0070370 | restrictive dermopathy 2 | HGNC:6636 | Homo sapiens (human) | 4000 | LMNA |
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| DOID:0070367 | leukoencephalopathy with vanishing white matter 5 | MGI:2446176 | Mus musculus (house mouse) | 224045 | Eif2b5 |
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| DOID:0070365 | nevoid basal cell carcinoma syndrome 1 | WB:WBGene00004210 | Caenorhabditis elegans | 173631 | ptc-3 |
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| DOID:0070365 | nevoid basal cell carcinoma syndrome 1 | MGI:105373 | Mus musculus (house mouse) | 19206 | Ptch1 |
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| DOID:0070365 | nevoid basal cell carcinoma syndrome 1 | FB:FBgn0003892 | Drosophila melanogaster (fruit fly) | 35851 | ptc |
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| DOID:0070365 | nevoid basal cell carcinoma syndrome 1 | HGNC:9585 | Homo sapiens (human) | 5727 | PTCH1 |
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| DOID:0070365 | nevoid basal cell carcinoma syndrome 1 | WB:WBGene00004208 | Caenorhabditis elegans | 174274 | ptc-1 |
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| DOID:0070357 | nephrotic syndrome type 20 | MGI:1918560 | Mus musculus (house mouse) | 71310 | Tbc1d9 |
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| DOID:0070357 | nephrotic syndrome type 20 | HGNC:29097 | Homo sapiens (human) | 23061 | TBC1D9B |
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| DOID:0070357 | nephrotic syndrome type 20 | MGI:1924045 | Mus musculus (house mouse) | 76795 | Tbc1d9b |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | MGI:2664902 | Mus musculus (house mouse) | 226778 | Mark1 |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | MGI:1920955 | Mus musculus (house mouse) | 232944 | Mark4 |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | HGNC:3332 | Homo sapiens (human) | 2011 | MARK2 |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | MGI:99638 | Mus musculus (house mouse) | 13728 | Mark2 |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | MGI:1341865 | Mus musculus (house mouse) | 17169 | Mark3 |
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| DOID:0070356 | visual impairment and progressive phthisis bulbi | HGNC:6897 | Homo sapiens (human) | 4140 | MARK3 |
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| DOID:0070355 | overactive bladder syndrome | HGNC:497 | Homo sapiens (human) | 8989 | TRPA1 |
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