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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
LM-GlycoRepo
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:0110699 | hypotrichosis 2 | HGNC:1802 | Homo sapiens (human) | 1041 | CDSN |
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| DOID:2043 | hepatitis B | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:12849 | autistic disorder | HGNC:14287 | Homo sapiens (human) | 57502 | NLGN4X |
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| DOID:0111662 | ectodermal dysplasia 14 | HGNC:1268 | Homo sapiens (human) | 54084 | TSPEAR |
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| DOID:3393 | coronary artery disease | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:219 | colon cancer | HGNC:173 | Homo sapiens (human) | 92 | ACVR2A |
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| DOID:9970 | obesity | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:959 | Homo sapiens (human) | 581 | BAX |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:4942 | Homo sapiens (human) | 3117 | HLA-DQA1 |
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| DOID:655 | inherited metabolic disorder | HGNC:983 | Homo sapiens (human) | 590 | BCHE |
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| DOID:13938 | amenorrhea | HGNC:3964 | Homo sapiens (human) | 2488 | FSHB |
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| DOID:10652 | Alzheimer's disease | HGNC:3467 | Homo sapiens (human) | 2099 | ESR1 |
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| DOID:12930 | dilated cardiomyopathy | HGNC:16932 | Homo sapiens (human) | 10529 | NEBL |
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| DOID:526 | human immunodeficiency virus infectious disease | HGNC:1641 | Homo sapiens (human) | 30835 | CD209 |
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| DOID:9976 | heroin dependence | HGNC:4232 | Homo sapiens (human) | 2668 | GDNF |
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| DOID:0090110 | immune dysregulation-polyendocrinopathy-enteropathy-X-linked syndrome | HGNC:19191 | Homo sapiens (human) | 81704 | DOCK8 |
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| DOID:0112159 | autosomal dominant nonsyndromic deafness 78 | HGNC:10911 | Homo sapiens (human) | 6558 | SLC12A2 |
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| DOID:0112022 | non-syndromic X-linked intellectual disability 21 | HGNC:5996 | Homo sapiens (human) | 11141 | IL1RAPL1 |
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| DOID:11198 | DiGeorge syndrome | HGNC:3084 | Homo sapiens (human) | 1855 | DVL1 |
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| DOID:4450 | renal cell carcinoma | HGNC:17071 | Homo sapiens (human) | 23081 | KDM4C |
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| DOID:0081267 | graft-versus-host disease | HGNC:5331 | Homo sapiens (human) | 64127 | NOD2 |
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| DOID:2352 | hemochromatosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0110937 | autosomal dominant osteopetrosis 1 | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:9538 | multiple myeloma | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:0111795 | congenital nystagmus 6 | HGNC:20145 | Homo sapiens (human) | 4935 | GPR143 |
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