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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:684 | hepatocellular carcinoma | HGNC:18590 | Homo sapiens (human) | 80339 | PNPLA3 |
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| DOID:0112379 | muscular dystrophy-dystroglycanopathy type B4 | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:3393 | coronary artery disease | HGNC:24678 | Homo sapiens (human) | 79068 | FTO |
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| DOID:848 | arthritis | HGNC:11919 | Homo sapiens (human) | 958 | CD40 |
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| DOID:0060774 | congenital diarrhea | HGNC:12781 | Homo sapiens (human) | 7482 | WNT2B |
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| DOID:127 | leiomyoma | HGNC:17582 | Homo sapiens (human) | 23522 | KAT6B |
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| DOID:3145 | hyperlipoproteinemia type III | HGNC:613 | Homo sapiens (human) | 348 | APOE |
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| DOID:0070229 | intrahepatic cholestasis of pregnancy 3 | HGNC:45 | Homo sapiens (human) | 5244 | ABCB4 |
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| DOID:12361 | Graves' disease | HGNC:12680 | Homo sapiens (human) | 7422 | VEGFA |
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| DOID:10983 | Alport syndrome | HGNC:2207 | Homo sapiens (human) | 1287 | COL4A5 |
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| DOID:657 | adenoma | HGNC:583 | Homo sapiens (human) | 324 | APC |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0070204 | familial partial lipodystrophy type 3 | HGNC:9236 | Homo sapiens (human) | 5468 | PPARG |
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| DOID:559 | acute pyelonephritis | HGNC:6027 | Homo sapiens (human) | 3579 | CXCR2 |
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| DOID:4189 | mutism | HGNC:13830 | Homo sapiens (human) | 26047 | CNTNAP2 |
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| DOID:7004 | ACTH-secreting pituitary adenoma | HGNC:12631 | Homo sapiens (human) | 9101 | USP8 |
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| DOID:0050073 | invasive aspergillosis | HGNC:2621 | Homo sapiens (human) | 1557 | CYP2C19 |
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| DOID:0112182 | mismatch repair cancer syndrome | HGNC:21686 | Homo sapiens (human) | 8635 | RNASET2 |
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| DOID:4450 | renal cell carcinoma | HGNC:74 | Homo sapiens (human) | 9429 | ABCG2 |
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| DOID:0081267 | graft-versus-host disease | HGNC:4940 | Homo sapiens (human) | 3115 | HLA-DPB1 |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:7468 | Homo sapiens (human) | 4548 | MTR |
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| DOID:0060805 | Prieto syndrome | HGNC:14543 | Homo sapiens (human) | 65267 | WNK3 |
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| DOID:1564 | fungal infectious disease | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1875 | impotence | HGNC:12828 | Homo sapiens (human) | 7515 | XRCC1 |
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| DOID:3121 | gallbladder cancer | HGNC:583 | Homo sapiens (human) | 324 | APC |
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