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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:2566 | corneal dystrophy | HGNC:14415 | Homo sapiens (human) | 6785 | ELOVL4 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:0060001 | withdrawal disorder | HGNC:8156 | Homo sapiens (human) | 4988 | OPRM1 |
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| DOID:9256 | colorectal cancer | HGNC:3373 | Homo sapiens (human) | 2033 | EP300 |
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| DOID:10534 | stomach cancer | HGNC:6016 | Homo sapiens (human) | 3567 | IL5 |
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| DOID:552 | pneumonia | HGNC:7097 | Homo sapiens (human) | 4282 | MIF |
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| DOID:11832 | visual epilepsy | HGNC:20766 | Homo sapiens (human) | 7846 | TUBA1A |
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| DOID:0060025 | immunoglobulin alpha deficiency | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0050746 | mantle cell lymphoma | HGNC:11904 | Homo sapiens (human) | 8797 | TNFRSF10A |
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| DOID:4586 | familial meningioma | HGNC:11109 | Homo sapiens (human) | 6605 | SMARCE1 |
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| DOID:0070301 | multiple epiphyseal dysplasia 6 | HGNC:2217 | Homo sapiens (human) | 1297 | COL9A1 |
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| DOID:11713 | diabetic angiopathy | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0080454 | developmental and epileptic encephalopathy 42 | HGNC:1388 | Homo sapiens (human) | 773 | CACNA1A |
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| DOID:2452 | thrombophilia | HGNC:9071 | Homo sapiens (human) | 5340 | PLG |
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| DOID:0060131 | alexithymia | HGNC:11050 | Homo sapiens (human) | 6532 | SLC6A4 |
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| DOID:10763 | hypertension | HGNC:4392 | Homo sapiens (human) | 2778 | GNAS |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:11537 | Homo sapiens (human) | 6874 | TAF4 |
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| DOID:9111 | cutaneous leishmaniasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:9256 | colorectal cancer | HGNC:2897 | Homo sapiens (human) | 10395 | DLC1 |
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| DOID:0111265 | Boucher-Neuhauser syndrome | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0060249 | scoliosis | HGNC:12008 | Homo sapiens (human) | 7166 | TPH1 |
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| DOID:4450 | renal cell carcinoma | HGNC:2505 | Homo sapiens (human) | 1493 | CTLA4 |
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| DOID:0110409 | retinitis pigmentosa 46 | HGNC:5385 | Homo sapiens (human) | 3420 | IDH3B |
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| DOID:0090134 | complex cortical dysplasia with other brain malformations 3 | HGNC:6318 | Homo sapiens (human) | 3796 | KIF2A |
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| DOID:0110860 | polycystic kidney disease 3 | HGNC:4138 | Homo sapiens (human) | 23193 | GANAB |
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