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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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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:0080162 | lupus nephritis | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:0080162 | lupus nephritis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0080162 | lupus nephritis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080159 | Cryptococcal meningitis | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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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 | MGI:96824 | Mus musculus (house mouse) | 21898 | Tlr4 |
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| DOID:0080158 | herpes simplex virus keratitis | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:0080158 | herpes simplex virus keratitis | RGD:3870 | Rattus norvegicus (Norway rat) | 29260 | Tlr4 |
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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 | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | 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:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | ZFIN:ZDB-GENE-040426-1086 | Danio rerio (zebrafish) | 791759 | piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | HGNC:8957 | Homo sapiens (human) | 5277 | PIGA |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | FB:FBgn0034270 | Drosophila melanogaster (fruit fly) | 37020 | PIG-A |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | MGI:99461 | Mus musculus (house mouse) | 18700 | Piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | Xenbase:XB-GENE-996765 | Xenopus tropicalis (tropical clawed frog) | 100158632 | piga |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | WB:WBGene00008431 | Caenorhabditis elegans | 174386 | piga-1 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | Xenbase:XB-GENE-6485976 | Xenopus laevis (African clawed frog) | 108707921 | piga.L |
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| DOID:0080138 | multiple congenital anomalies-hypotonia-seizures syndrome 1 | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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