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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:0080228 | autosomal dominant intellectual developmental disorder 53 | RGD:2261 | Rattus norvegicus (Norway rat) | 25400 | Camk2a |
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| DOID:0080228 | autosomal dominant intellectual developmental disorder 53 | HGNC:1460 | Homo sapiens (human) | 815 | CAMK2A |
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| DOID:0080228 | autosomal dominant intellectual developmental disorder 53 | MGI:88256 | Mus musculus (house mouse) | 12322 | Camk2a |
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| DOID:0080227 | autosomal dominant intellectual developmental disorder 55 | MGI:1196365 | Mus musculus (house mouse) | 52014 | Nus1 |
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| DOID:0080227 | autosomal dominant intellectual developmental disorder 55 | HGNC:21042 | Homo sapiens (human) | 116150 | NUS1 |
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| DOID:0080227 | autosomal dominant intellectual developmental disorder 55 | ZFIN:ZDB-GENE-040718-48 | Danio rerio (zebrafish) | 436629 | nus1 |
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| DOID:0080226 | autosomal dominant intellectual developmental disorder 56 | MGI:2388633 | Mus musculus (house mouse) | 67300 | Cltc |
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| DOID:0080226 | autosomal dominant intellectual developmental disorder 56 | HGNC:2092 | Homo sapiens (human) | 1213 | CLTC |
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| DOID:0080224 | autosomal dominant dystrophic epidermolysis bullosa | HGNC:2214 | Homo sapiens (human) | 1294 | COL7A1 |
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| DOID:0080224 | autosomal dominant dystrophic epidermolysis bullosa | MGI:88462 | Mus musculus (house mouse) | 12836 | Col7a1 |
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| DOID:0080222 | pseudohypoparathyroidism type IB | MGI:95777 | Mus musculus (house mouse) | 14683 | Gnas |
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| DOID:0080222 | pseudohypoparathyroidism type IB | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0080219 | dystransthyretinemic hyperthyroxinemia | HGNC:12405 | Homo sapiens (human) | 7276 | TTR |
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| DOID:0080219 | dystransthyretinemic hyperthyroxinemia | MGI:98865 | Mus musculus (house mouse) | 22139 | Ttr |
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| DOID:0080219 | dystransthyretinemic hyperthyroxinemia | Xenbase:XB-GENE-865269 | Xenopus laevis (African clawed frog) | 397787 | ttr.L |
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| DOID:0080219 | dystransthyretinemic hyperthyroxinemia | RGD:3916 | Rattus norvegicus (Norway rat) | 24856 | Ttr |
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| DOID:0080218 | primary spontaneous pneumothorax | HGNC:27310 | Homo sapiens (human) | 201163 | FLCN |
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| DOID:0080217 | lysosomal acid lipase deficiency | WB:WBGene00009773 | Caenorhabditis elegans | 185840 | lipl-2 |
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| DOID:0080217 | lysosomal acid lipase deficiency | WB:WBGene00022642 | Caenorhabditis elegans | 178563 | lipl-5 |
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| DOID:0080217 | lysosomal acid lipase deficiency | WB:WBGene00020016 | Caenorhabditis elegans | 178572 | lipl-3 |
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| DOID:0080217 | lysosomal acid lipase deficiency | MGI:96789 | Mus musculus (house mouse) | 16889 | Lipa |
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| DOID:0080217 | lysosomal acid lipase deficiency | FB:FBgn0023495 | Drosophila melanogaster (fruit fly) | 41643 | Lip3 |
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| DOID:0080217 | lysosomal acid lipase deficiency | WB:WBGene00019376 | Caenorhabditis elegans | 179046 | lipl-4 |
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| DOID:0080217 | lysosomal acid lipase deficiency | HGNC:6617 | Homo sapiens (human) | 3988 | LIPA |
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| DOID:0080217 | lysosomal acid lipase deficiency | WB:WBGene00010062 | Caenorhabditis elegans | 179771 | lipl-1 |
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