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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:0070332 | multiple mitochondrial dysfunctions syndrome 6 | MGI:107876 | Mus musculus (house mouse) | 22273 | Uqcrc1 |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | HGNC:9119 | Homo sapiens (human) | 9512 | PMPCB |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | RGD:1303314 | Rattus norvegicus (Norway rat) | 301011 | Uqcrc1 |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | MGI:1920328 | Mus musculus (house mouse) | 73078 | Pmpcb |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | HGNC:12585 | Homo sapiens (human) | 7384 | UQCRC1 |
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| DOID:0070330 | multiple mitochondrial dysfunctions syndrome | HGNC:4208 | Homo sapiens (human) | 2653 | GCSH |
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| DOID:0070329 | mitochondrial DNA depletion syndrome | MGI:1353497 | Mus musculus (house mouse) | 27376 | Slc25a10 |
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| DOID:0070329 | mitochondrial DNA depletion syndrome | HGNC:10980 | Homo sapiens (human) | 1468 | SLC25A10 |
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| DOID:0070316 | Miura type epiphyseal chondrodysplasia | HGNC:7944 | Homo sapiens (human) | 4882 | NPR2 |
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| DOID:0070316 | Miura type epiphyseal chondrodysplasia | WB:WBGene00020131 | Caenorhabditis elegans | 172051 | gcy-28 |
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| DOID:0070316 | Miura type epiphyseal chondrodysplasia | RGD:620851 | Rattus norvegicus (Norway rat) | 116564 | Npr2 |
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| DOID:0070316 | Miura type epiphyseal chondrodysplasia | MGI:97372 | Mus musculus (house mouse) | 230103 | Npr2 |
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| DOID:0070314 | obstructive nephropathy | HGNC:18234 | Homo sapiens (human) | 55034 | MOCOS |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:15872 | Homo sapiens (human) | 26074 | CFAP61 |
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| DOID:0070311 | oligoasthenoteratozoospermia | MGI:1333754 | Mus musculus (house mouse) | 15463 | Agfg1 |
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| DOID:0070311 | oligoasthenoteratozoospermia | RGD:1560041 | Rattus norvegicus (Norway rat) | 363266 | Agfg1 |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:26125 | Homo sapiens (human) | 64847 | SPATA20 |
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| DOID:0070311 | oligoasthenoteratozoospermia | RGD:735087 | Rattus norvegicus (Norway rat) | 360604 | Spata20 |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:9319 | Homo sapiens (human) | 5531 | PPP4C |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:5175 | Homo sapiens (human) | 3267 | AGFG1 |
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| DOID:0070311 | oligoasthenoteratozoospermia | HGNC:26676 | Homo sapiens (human) | 159686 | CFAP58 |
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| DOID:0070311 | oligoasthenoteratozoospermia | MGI:2183449 | Mus musculus (house mouse) | 217116 | Spata20 |
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| DOID:0070311 | oligoasthenoteratozoospermia | WB:WBGene00015204 | Caenorhabditis elegans | 174243 | B0495.5 |
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| DOID:0070309 | absence epilepsy | MGI:109482 | Mus musculus (house mouse) | 12286 | Cacna1a |
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| DOID:0070309 | absence epilepsy | RGD:2244 | Rattus norvegicus (Norway rat) | 25398 | Cacna1a |
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