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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:0070048 | GAND syndrome | HGNC:30778 | Homo sapiens (human) | 57459 | GATAD2B |
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| DOID:0070048 | GAND syndrome | MGI:2443225 | Mus musculus (house mouse) | 229542 | Gatad2b |
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| DOID:0070047 | Schuurs-Hoeijmakers Syndrome | MGI:1277113 | Mus musculus (house mouse) | 107975 | Pacs1 |
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| DOID:0070047 | Schuurs-Hoeijmakers Syndrome | RGD:620579 | Rattus norvegicus (Norway rat) | 171444 | Pacs1 |
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| DOID:0070047 | Schuurs-Hoeijmakers Syndrome | HGNC:30032 | Homo sapiens (human) | 55690 | PACS1 |
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| DOID:0070046 | Coffin-Siris syndrome 4 | HGNC:11100 | Homo sapiens (human) | 6597 | SMARCA4 |
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| DOID:0070046 | Coffin-Siris syndrome 4 | MGI:88192 | Mus musculus (house mouse) | 20586 | Smarca4 |
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| DOID:0070046 | Coffin-Siris syndrome 4 | SGD:S000005816 | Saccharomyces cerevisiae S288C | 854465 | SNF2 |
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| DOID:0070045 | Coffin-Siris syndrome 3 | HGNC:11103 | Homo sapiens (human) | 6598 | SMARCB1 |
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| DOID:0070045 | Coffin-Siris syndrome 3 | SGD:S000000493 | Saccharomyces cerevisiae S288C | 852592 | SNF5 |
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| DOID:0070044 | Coffin-Siris syndrome 2 | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0070044 | Coffin-Siris syndrome 2 | MGI:1935147 | Mus musculus (house mouse) | 93760 | Arid1a |
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| DOID:0070043 | autosomal dominant intellectual developmental disorder 13 | RGD:2511 | Rattus norvegicus (Norway rat) | 29489 | Dync1h1 |
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| DOID:0070043 | autosomal dominant intellectual developmental disorder 13 | MGI:103147 | Mus musculus (house mouse) | 13424 | Dync1h1 |
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| DOID:0070043 | autosomal dominant intellectual developmental disorder 13 | HGNC:2961 | Homo sapiens (human) | 1778 | DYNC1H1 |
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| DOID:0070042 | Coffin-Siris syndrome 1 | MGI:1935147 | Mus musculus (house mouse) | 93760 | Arid1a |
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| DOID:0070042 | Coffin-Siris syndrome 1 | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0070041 | autosomal dominant intellectual developmental disorder 11 | RGD:71087 | Rattus norvegicus (Norway rat) | 59317 | Epb41l1 |
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| DOID:0070041 | autosomal dominant intellectual developmental disorder 11 | FB:FBgn0010434 | Drosophila melanogaster (fruit fly) | 37205 | cora |
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| DOID:0070041 | autosomal dominant intellectual developmental disorder 11 | MGI:103010 | Mus musculus (house mouse) | 13821 | Epb41l1 |
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| DOID:0070041 | autosomal dominant intellectual developmental disorder 11 | HGNC:3378 | Homo sapiens (human) | 2036 | EPB41L1 |
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| DOID:0070040 | autosomal dominant intellectual developmental disorder 10 | HGNC:1406 | Homo sapiens (human) | 10369 | CACNG2 |
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| DOID:0070040 | autosomal dominant intellectual developmental disorder 10 | MGI:1316660 | Mus musculus (house mouse) | 12300 | Cacng2 |
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| DOID:0070040 | autosomal dominant intellectual developmental disorder 10 | RGD:71095 | Rattus norvegicus (Norway rat) | 84347 | Cacng2 |
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| DOID:0070038 | autosomal dominant intellectual developmental disorder 8 | Xenbase:XB-GENE-17335935 | Xenopus laevis (African clawed frog) | 108699855 | grin1.S |
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