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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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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:1287 | cardiovascular system disease | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0110013 | advanced sleep phase syndrome 3 | HGNC:8847 | Homo sapiens (human) | 8863 | PER3 |
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| DOID:5844 | myocardial infarction | HGNC:602 | Homo sapiens (human) | 337 | APOA4 |
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| DOID:2349 | arteriosclerosis | HGNC:8941 | Homo sapiens (human) | 5265 | SERPINA1 |
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| DOID:0111594 | distal arthrogryposis type 5D | HGNC:3147 | Homo sapiens (human) | 9427 | ECEL1 |
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| DOID:3312 | bipolar disorder | HGNC:701 | Homo sapiens (human) | 406 | BMAL1 |
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| DOID:0110068 | frontotemporal dementia and/or amyotrophic lateral sclerosis 3 | HGNC:11280 | Homo sapiens (human) | 8878 | SQSTM1 |
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| DOID:8778 | Crohn's disease | HGNC:10969 | Homo sapiens (human) | 6584 | SLC22A5 |
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| DOID:684 | hepatocellular carcinoma | HGNC:11848 | Homo sapiens (human) | 7097 | TLR2 |
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| DOID:0111626 | D-glyceric aciduria | HGNC:24247 | Homo sapiens (human) | 132158 | GLYCTK |
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| DOID:2841 | asthma | HGNC:5991 | Homo sapiens (human) | 3552 | IL1A |
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| DOID:0111899 | X-linked thrombophilia due to factor IX defect | HGNC:3551 | Homo sapiens (human) | 2158 | F9 |
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| DOID:0111381 | IVIC syndrome | HGNC:15924 | Homo sapiens (human) | 57167 | SALL4 |
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| DOID:0080244 | Galloway-Mowat syndrome 2 | HGNC:26058 | Homo sapiens (human) | 8270 | LAGE3 |
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| DOID:1240 | leukemia | HGNC:16496 | Homo sapiens (human) | 23305 | ACSL6 |
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| DOID:3717 | gastric adenocarcinoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0112382 | muscular dystrophy-dystroglycanopathy type C8 | HGNC:25902 | Homo sapiens (human) | 84892 | POMGNT2 |
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| DOID:0050848 | obstructive sleep apnea | HGNC:7997 | Homo sapiens (human) | 3084 | NRG1 |
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| DOID:0060041 | autism spectrum disorder | HGNC:6140 | Homo sapiens (human) | 3676 | ITGA4 |
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| DOID:1485 | cystic fibrosis | HGNC:4886 | Homo sapiens (human) | 3077 | HFE |
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| DOID:0090141 | cortisone reductase deficiency 1 | HGNC:4795 | Homo sapiens (human) | 9563 | H6PD |
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| DOID:2596 | larynx cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0111588 | Greenberg dysplasia | HGNC:6518 | Homo sapiens (human) | 3930 | LBR |
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| DOID:0070122 | Meckel syndrome 8 | HGNC:25774 | Homo sapiens (human) | 79867 | TCTN2 |
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| DOID:12377 | spinal muscular atrophy | HGNC:12649 | Homo sapiens (human) | 9217 | VAPB |
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