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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:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:2986 | Homo sapiens (human) | 8447 | DOC2B |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | RGD:1305501 | Rattus norvegicus (Norway rat) | 293481 | Tufm |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | RGD:620073 | Rattus norvegicus (Norway rat) | 171039 | Rph3a |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | MGI:102788 | Mus musculus (house mouse) | 19894 | Rph3a |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:29259 | Homo sapiens (human) | 57551 | TAOK1 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | MGI:1923686 | Mus musculus (house mouse) | 233870 | Tufm |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:11605 | Homo sapiens (human) | 6911 | TBX6 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:16835 | Homo sapiens (human) | 9344 | TAOK2 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | MGI:2446242 | Mus musculus (house mouse) | 233871 | Atxn2l |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | Xenbase:XB-GENE-5998370 | Xenopus tropicalis (tropical clawed frog) | 100216215 | asphd2 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:31326 | Homo sapiens (human) | 11273 | ATXN2L |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:28707 | Homo sapiens (human) | 79447 | PAGR1 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | MGI:1914186 | Mus musculus (house mouse) | 65973 | Asph |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | MGI:1277223 | Mus musculus (house mouse) | 20239 | Atxn2 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:10555 | Homo sapiens (human) | 6311 | ATXN2 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | MGI:107688 | Mus musculus (house mouse) | 16569 | Kif3b |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | FB:FBgn0041188 | Drosophila melanogaster (fruit fly) | 41883 | Atx2 |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:6321 | Homo sapiens (human) | 3797 | KIF3C |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:1769 | Homo sapiens (human) | 10423 | CDIPT |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:9319 | Homo sapiens (human) | 5531 | PPP4C |
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| DOID:0070515 | chromosome 16p11.2 deletion syndrome, 593-kb | HGNC:757 | Homo sapiens (human) | 444 | ASPH |
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| DOID:0070514 | neurodevelopmental disorder with dysmorphic facies and distal limb anomalies | FB:FBgn0000541 | Drosophila melanogaster (fruit fly) | 44811 | E(bx) |
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| DOID:0070514 | neurodevelopmental disorder with dysmorphic facies and distal limb anomalies | HGNC:3581 | Homo sapiens (human) | 2186 | BPTF |
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| DOID:0070511 | polyhydramnios, megalencephaly, and symptomatic epilepsy | HGNC:30172 | Homo sapiens (human) | 92335 | STRADA |
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| DOID:0070509 | Schinzel Giedion syndrome | HGNC:15573 | Homo sapiens (human) | 26040 | SETBP1 |
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