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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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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:1993 | rectum cancer | HGNC:6848 | Homo sapiens (human) | 4214 | MAP3K1 |
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| DOID:9828 | neonatal abstinence syndrome | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:8924 | autoimmune thrombocytopenic purpura | HGNC:6014 | Homo sapiens (human) | 3565 | IL4 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | HGNC:5006 | Homo sapiens (human) | 3156 | HMGCR |
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| DOID:12365 | malaria | HGNC:4035 | Homo sapiens (human) | 2532 | ACKR1 |
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| DOID:0080236 | autosomal dominant intellectual developmental disorder 45 | HGNC:14214 | Homo sapiens (human) | 23152 | CIC |
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| DOID:0050650 | familial atrial fibrillation | HGNC:777 | Homo sapiens (human) | 463 | ZFHX3 |
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| DOID:9268 | glycine encephalopathy | HGNC:473 | Homo sapiens (human) | 275 | AMT |
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| DOID:0111312 | idiopathic generalized epilepsy 11 | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:6196 | reactive arthritis | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0111938 | immunodeficiency 24 | HGNC:2519 | Homo sapiens (human) | 1503 | CTPS1 |
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| DOID:11335 | sarcoidosis | HGNC:19100 | Homo sapiens (human) | 149233 | IL23R |
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| DOID:0080770 | autosomal dominant beta thalassemia | HGNC:4827 | Homo sapiens (human) | 3043 | HBB |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:10533 | viral pneumonia | HGNC:15633 | Homo sapiens (human) | 54106 | TLR9 |
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| DOID:218 | ascending colon cancer | HGNC:9177 | Homo sapiens (human) | 5426 | POLE |
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| DOID:0081002 | Cowden syndrome 6 | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:9975 | cocaine dependence | HGNC:1464 | Homo sapiens (human) | 814 | CAMK4 |
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| DOID:9164 | achalasia | HGNC:13666 | Homo sapiens (human) | 8086 | AAAS |
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| DOID:2565 | macular corneal dystrophy | HGNC:6938 | Homo sapiens (human) | 4166 | CHST6 |
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| DOID:12783 | migraine without aura | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:850 | lung disease | HGNC:3179 | Homo sapiens (human) | 1909 | EDNRA |
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| DOID:13514 | venous tributary occlusion of retina | HGNC:6137 | Homo sapiens (human) | 3673 | ITGA2 |
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| DOID:0070165 | spermatogenic failure 18 | HGNC:2940 | Homo sapiens (human) | 25981 | DNAH1 |
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| DOID:0111954 | immunodeficiency 60 | HGNC:14078 | Homo sapiens (human) | 60468 | BACH2 |
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