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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:4988 | alcoholic pancreatitis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:13258 | typhoid fever | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:11132 | prostatic hypertrophy | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:10652 | Alzheimer's disease | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0111864 | autosomal recessive congenital bilateral absence of vas deferens | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:1724 | duodenal ulcer | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:10808 | gastric ulcer | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:0111862 | congenital bilateral absence of vas deferens | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:10211 | cholelithiasis | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:2841 | asthma | HGNC:1884 | Homo sapiens (human) | 1080 | CFTR |
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| DOID:12134 | factor VIII deficiency | HGNC:8864 | Homo sapiens (human) | 5199 | CFP |
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| DOID:0111768 | X-linked properdin deficiency | HGNC:8864 | Homo sapiens (human) | 5199 | CFP |
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| DOID:1184 | nephrotic syndrome | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:767 | muscular atrophy | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0050562 | West syndrome | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:4948 | gallbladder carcinoma | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:5844 | myocardial infarction | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:1824 | status epilepticus | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:11457 | brain compression | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:5199 | ureteral obstruction | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0110934 | nemaline myopathy 7 | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:1574 | alcohol use disorder | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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| DOID:1875 | impotence | HGNC:1874 | Homo sapiens (human) | 1072 | CFL1 |
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