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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:0070353 | cataract 47 | SGD:S000005833 | Saccharomyces cerevisiae S288C | 854483 | MCH5 |
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| DOID:0070353 | cataract 47 | SGD:S000005069 | Saccharomyces cerevisiae S288C | 855598 | ESBP6 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | RGD:620387 | Rattus norvegicus (Norway rat) | 83507 | Parg |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | WB:WBGene00004052 | Caenorhabditis elegans | 186765 | parg-2 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | FB:FBgn0023216 | Drosophila melanogaster (fruit fly) | 31329 | Parg |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:1094 | Homo sapiens (human) | 670 | BPHL |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | Xenbase:XB-GENE-944445 | Xenopus tropicalis (tropical clawed frog) | 548938 | adprs |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | MGI:2140364 | Mus musculus (house mouse) | 100206 | Adprs |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | WB:WBGene00004051 | Caenorhabditis elegans | 177683 | parg-1 |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:21304 | Homo sapiens (human) | 54936 | ADPRS |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | ZFIN:ZDB-GENE-040912-85 | Danio rerio (zebrafish) | 796446 | adprs |
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| DOID:0070351 | spinal muscular atrophy with lower extremity predominant 1 | HGNC:2961 | Homo sapiens (human) | 1778 | DYNC1H1 |
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| DOID:0070351 | spinal muscular atrophy with lower extremity predominant 1 | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0070351 | spinal muscular atrophy with lower extremity predominant 1 | RGD:2511 | Rattus norvegicus (Norway rat) | 29489 | Dync1h1 |
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| DOID:0070347 | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:0070347 | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | HGNC:2973 | Homo sapiens (human) | 10059 | DNM1L |
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| DOID:0070347 | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | RGD:620416 | Rattus norvegicus (Norway rat) | 114114 | Dnm1l |
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| DOID:0070346 | neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies | MGI:1915760 | Mus musculus (house mouse) | 68510 | Ints1 |
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| DOID:0070346 | neurodevelopmental disorder with cataracts, poor growth, and dysmorphic facies | HGNC:24555 | Homo sapiens (human) | 26173 | INTS1 |
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| DOID:0070345 | vertebral anomalies and variable endocrine and T-cell dysfunction | HGNC:11597 | Homo sapiens (human) | 6909 | TBX2 |
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| DOID:0070344 | ocular tuberculosis | MGI:96537 | Mus musculus (house mouse) | 16153 | Il10 |
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| DOID:0070344 | ocular tuberculosis | RGD:2886 | Rattus norvegicus (Norway rat) | 25325 | Il10 |
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| DOID:0070344 | ocular tuberculosis | HGNC:5962 | Homo sapiens (human) | 3586 | IL10 |
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| DOID:0070343 | CSF1R-related brain malformation and osteopetrosis | WB:WBGene00006894 | Caenorhabditis elegans | 175182 | ver-1 |
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