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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:8778 | Crohn's disease | HGNC:10907 | Homo sapiens (human) | 6556 | SLC11A1 |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:17675 | Homo sapiens (human) | 57510 | XPO5 |
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| DOID:3068 | glioblastoma | HGNC:2926 | Homo sapiens (human) | 1755 | DMBT1 |
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| DOID:12894 | Sjogren's syndrome | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:769 | neuroblastoma | HGNC:11110 | Homo sapiens (human) | 8289 | ARID1A |
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| DOID:12387 | nephrogenic diabetes insipidus | RGD:1306831 | Rattus norvegicus (Norway rat) | 361618 | Stim1 |
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| DOID:0080688 | mosaic variegated aneuploidy syndrome | HGNC:20465 | Homo sapiens (human) | 23137 | SMC5 |
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| DOID:2256 | osteochondrodysplasia | HGNC:9608 | Homo sapiens (human) | 5745 | PTH1R |
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| DOID:3393 | coronary artery disease | HGNC:13916 | Homo sapiens (human) | 55937 | APOM |
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| DOID:1312 | focal segmental glomerulosclerosis | HGNC:14258 | Homo sapiens (human) | 23607 | CD2AP |
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| DOID:10584 | retinitis pigmentosa | HGNC:18121 | Homo sapiens (human) | 83552 | MFRP |
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| DOID:0070441 | retinal macular dystrophy 4 | HGNC:11891 | Homo sapiens (human) | 7123 | CLEC3B |
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| DOID:5419 | schizophrenia | HGNC:1396 | Homo sapiens (human) | 8911 | CACNA1I |
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| DOID:9119 | acute myeloid leukemia | HGNC:11761 | Homo sapiens (human) | 7980 | TFPI2 |
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| DOID:0080258 | autosomal recessive congenital ichthyosis 14 | HGNC:11459 | Homo sapiens (human) | 6820 | SULT2B1 |
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| DOID:0060704 | lymphoproliferative syndrome | HGNC:6340 | Homo sapiens (human) | 3813 | KIR3DS1 |
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| DOID:10024 | migraine with aura | HGNC:2689 | Homo sapiens (human) | 1621 | DBH |
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| DOID:0111105 | maturity-onset diabetes of the young type 8 | HGNC:1848 | Homo sapiens (human) | 1056 | CEL |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:10760 | Homo sapiens (human) | 6418 | SET |
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| DOID:684 | hepatocellular carcinoma | HGNC:6005 | Homo sapiens (human) | 59067 | IL21 |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:4187 | Homo sapiens (human) | 2638 | GC |
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| DOID:0112012 | X-linked mutilating palmoplantar keratoderma with periorificial keratotic plaques | HGNC:15455 | Homo sapiens (human) | 51360 | MBTPS2 |
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| DOID:1067 | open-angle glaucoma | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:13523 | Homo sapiens (human) | 10332 | CLEC4M |
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| DOID:0060366 | Hennekam syndrome | HGNC:29426 | Homo sapiens (human) | 147372 | CCBE1 |
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