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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID ▲ | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:1273 | respiratory syncytial virus infectious disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:2841 | asthma | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:11650 | bronchopulmonary dysplasia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:3827 | congenital diaphragmatic hernia | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:850 | lung disease | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:1485 | cystic fibrosis | HGNC:10798 | Homo sapiens (human) | 653509 | SFTPA1 |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0050573 | 2-hydroxyglutaric aciduria | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:11198 | DiGeorge syndrome | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0111619 | combined D-2- and L-2-hydroxyglutaric aciduria | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:9970 | obesity | HGNC:21298 | Homo sapiens (human) | 65985 | AACS |
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| DOID:10652 | Alzheimer's disease | RGD:620150 | Rattus norvegicus (Norway rat) | 66020 | Gapdhs |
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| DOID:0070112 | Niemann-Pick disease type B | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:14504 | Niemann-Pick disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:0070111 | Niemann-Pick disease type A | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:893 | Wilson disease | HGNC:11120 | Homo sapiens (human) | 6609 | SMPD1 |
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| DOID:684 | hepatocellular carcinoma | MGI:1913440 | Mus musculus (house mouse) | 66190 | Acer3 |
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| DOID:10579 | leukodystrophy | MGI:1913440 | Mus musculus (house mouse) | 66190 | Acer3 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | MGI:1913440 | Mus musculus (house mouse) | 66190 | Acer3 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1913498 | Mus musculus (house mouse) | 66248 | Alg5 |
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| DOID:0080322 | polycystic kidney disease | MGI:1913498 | Mus musculus (house mouse) | 66248 | Alg5 |
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| DOID:12140 | Chagas disease | HGNC:11177 | Homo sapiens (human) | 6646 | SOAT1 |
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