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GlyTouCan
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:0070044 | Coffin-Siris syndrome 2 | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:769 | neuroblastoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:1574 | alcohol use disorder | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:9261 | nasopharynx carcinoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:4927 | Klatskin's tumor | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0050934 | ovarian clear cell carcinoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0070042 | Coffin-Siris syndrome 1 | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:4928 | intrahepatic cholangiocarcinoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:0050564 | autosomal dominant nonsyndromic deafness | HGNC:12347 | Homo sapiens (human) | 8295 | TRRAP |
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| DOID:0112166 | autosomal dominant nonsyndromic deafness 75 | HGNC:12347 | Homo sapiens (human) | 8295 | TRRAP |
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| DOID:9119 | acute myeloid leukemia | HGNC:15514 | Homo sapiens (human) | 8301 | PICALM |
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| DOID:0111067 | congenital bile acid synthesis defect 6 | HGNC:120 | Homo sapiens (human) | 8309 | ACOX2 |
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| DOID:865 | vasculitis | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:14330 | Parkinson's disease | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:0110663 | congenital myasthenic syndrome 1A | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:2316 | brain ischemia | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:8893 | psoriasis | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:1574 | alcohol use disorder | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:0070526 | PLACK syndrome | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:7148 | rheumatoid arthritis | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:12894 | Sjogren's syndrome | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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| DOID:10652 | Alzheimer's disease | HGNC:1515 | Homo sapiens (human) | 831 | CAST |
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