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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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0060419 | chromosome 3q29 microdeletion syndrome | RGD:620131 | Rattus norvegicus (Norway rat) | 117099 | Bdh1 |
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| DOID:0060419 | chromosome 3q29 microdeletion syndrome | WB:WBGene00012182 | Caenorhabditis elegans | 175140 | osta-3 |
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| DOID:0060419 | chromosome 3q29 microdeletion syndrome | HGNC:11740 | Homo sapiens (human) | 7018 | TF |
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| DOID:0060419 | chromosome 3q29 microdeletion syndrome | MGI:1351670 | Mus musculus (house mouse) | 27400 | Hsd17b6 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | MGI:1332635 | Mus musculus (house mouse) | 18100 | Mrpl40 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:11133 | Homo sapiens (human) | 9342 | SNAP29 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:8983 | Homo sapiens (human) | 5297 | PI4KA |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:17325 | Homo sapiens (human) | 58510 | PRODH2 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:4916 | Homo sapiens (human) | 7290 | HIRA |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | MGI:2448506 | Mus musculus (house mouse) | 224020 | Pi4ka |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | MGI:2137379 | Mus musculus (house mouse) | 94112 | Med15 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | MGI:1914724 | Mus musculus (house mouse) | 67474 | Snap29 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:14248 | Homo sapiens (human) | 51586 | MED15 |
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| DOID:0060412 | chromosome 1q41-q42 deletion syndrome | MGI:2138319 | Mus musculus (house mouse) | 209456 | Trp53bp2 |
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| DOID:0060412 | chromosome 1q41-q42 deletion syndrome | HGNC:12000 | Homo sapiens (human) | 7159 | TP53BP2 |
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| DOID:0060411 | chromosome 1q21.1 deletion syndrome | MGI:1933114 | Mus musculus (house mouse) | 80288 | Bcl9l |
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| DOID:0060411 | chromosome 1q21.1 deletion syndrome | HGNC:23688 | Homo sapiens (human) | 283149 | BCL9L |
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| DOID:0060411 | chromosome 1q21.1 deletion syndrome | MGI:1924828 | Mus musculus (house mouse) | 77578 | Bcl9 |
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| DOID:0060411 | chromosome 1q21.1 deletion syndrome | HGNC:1008 | Homo sapiens (human) | 607 | BCL9 |
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| DOID:0060410 | chromosome 1p36 deletion syndrome | HGNC:6229 | Homo sapiens (human) | 8514 | KCNAB2 |
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| DOID:0060410 | chromosome 1p36 deletion syndrome | HGNC:26002 | Homo sapiens (human) | 54897 | CASZ1 |
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| DOID:0060410 | chromosome 1p36 deletion syndrome | MGI:1196251 | Mus musculus (house mouse) | 69743 | Casz1 |
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| DOID:0060410 | chromosome 1p36 deletion syndrome | MGI:109239 | Mus musculus (house mouse) | 16498 | Kcnab2 |
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| DOID:0060409 | NFIA-related disorder | MGI:108056 | Mus musculus (house mouse) | 18027 | Nfia |
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| DOID:0060409 | NFIA-related disorder | HGNC:7784 | Homo sapiens (human) | 4774 | NFIA |
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