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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species ▲ | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:3371 | chondrosarcoma | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:3458 | breast adenocarcinoma | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:700 | mitochondrial metabolism disease | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:8506 | bullous pemphigoid | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:14115 | toxic shock syndrome | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:3910 | lung adenocarcinoma | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:0080000 | muscular disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
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| DOID:1574 | alcohol use disorder | HGNC:14942 | Homo sapiens (human) | 79660 | PPP1R3B |
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| DOID:4947 | cholangiocarcinoma | HGNC:12541 | Homo sapiens (human) | 54600 | UGT1A9 |
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| DOID:3132 | porphyria cutanea tarda | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0050729 | Chanarin-Dorfman syndrome | HGNC:30802 | Homo sapiens (human) | 57104 | PNPLA2 |
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| DOID:8566 | herpes simplex | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:11476 | osteoporosis | HGNC:6697 | Homo sapiens (human) | 4041 | LRP5 |
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| DOID:3587 | pancreatic ductal carcinoma | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:10886 | Homo sapiens (human) | 22933 | SIRT2 |
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| DOID:552 | pneumonia | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:1070 | primary open angle glaucoma | HGNC:2597 | Homo sapiens (human) | 1545 | CYP1B1 |
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| DOID:2841 | asthma | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:1612 | breast cancer | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:9970 | obesity | HGNC:385 | Homo sapiens (human) | 1646 | AKR1C2 |
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| DOID:77 | gastrointestinal system disease | HGNC:5466 | Homo sapiens (human) | 3481 | IGF2 |
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| DOID:0050830 | peripheral artery disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:1289 | neurodegenerative disease | HGNC:9039 | Homo sapiens (human) | 8398 | PLA2G6 |
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| DOID:0060307 | autosomal dominant intellectual developmental disorder | HGNC:19263 | Homo sapiens (human) | 81562 | LMAN2L |
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| DOID:1682 | congenital heart disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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