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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:3526 | cerebral infarction | HGNC:4948 | Homo sapiens (human) | 3123 | HLA-DRB1 |
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| DOID:9296 | cleft lip | HGNC:7432 | Homo sapiens (human) | 4522 | MTHFD1 |
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| DOID:1287 | cardiovascular system disease | HGNC:4271 | Homo sapiens (human) | 2696 | GIPR |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:7458 | Homo sapiens (human) | 4537 | ND3 |
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| DOID:2218 | blood platelet disease | HGNC:3749 | Homo sapiens (human) | 2313 | FLI1 |
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| DOID:1459 | hypothyroidism | HGNC:12372 | Homo sapiens (human) | 7252 | TSHB |
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| DOID:418 | systemic scleroderma | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
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| DOID:0050686 | organ system cancer | HGNC:5994 | Homo sapiens (human) | 7850 | IL1R2 |
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| DOID:13564 | aspergillosis | HGNC:16711 | Homo sapiens (human) | 10333 | TLR6 |
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| DOID:1172 | hyperlipoproteinemia type IV | HGNC:17288 | Homo sapiens (human) | 116519 | APOA5 |
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| DOID:12365 | malaria | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:13777 | epidermodysplasia verruciformis | HGNC:18021 | Homo sapiens (human) | 11322 | TMC6 |
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| DOID:0111412 | exudative vitreoretinopathy 1 | HGNC:4042 | Homo sapiens (human) | 8322 | FZD4 |
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| DOID:12559 | idiopathic juvenile osteoporosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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| DOID:1324 | lung cancer | HGNC:12836 | Homo sapiens (human) | 22803 | XRN2 |
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| DOID:0080202 | adenoid cystic carcinoma | HGNC:12637 | Homo sapiens (human) | 7403 | KDM6A |
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| DOID:12930 | dilated cardiomyopathy | HGNC:7778 | Homo sapiens (human) | 4776 | NFATC4 |
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| DOID:0111969 | immunodeficiency 39 | HGNC:6122 | Homo sapiens (human) | 3665 | IRF7 |
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| DOID:5419 | schizophrenia | HGNC:3033 | Homo sapiens (human) | 1822 | ATN1 |
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| DOID:0080006 | bone development disease | HGNC:3755 | Homo sapiens (human) | 2317 | FLNB |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:11555 | Fuchs' endothelial dystrophy | HGNC:26504 | Homo sapiens (human) | 123624 | AGBL1 |
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| DOID:2043 | hepatitis B | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:0110857 | posterior polymorphous corneal dystrophy 3 | HGNC:11642 | Homo sapiens (human) | 6935 | ZEB1 |
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