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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:1793 | pancreatic cancer | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:12783 | migraine without aura | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:3622 | Homo sapiens (human) | 2218 | FKTN |
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| DOID:783 | end stage renal disease | HGNC:4323 | Homo sapiens (human) | 2739 | GLO1 |
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| DOID:3312 | bipolar disorder | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0112333 | pontocerebellar hypoplasia type 16 | HGNC:7102 | Homo sapiens (human) | 9562 | MINPP1 |
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| DOID:0081330 | glycogen storage disease Ib | HGNC:4061 | Homo sapiens (human) | 2542 | SLC37A4 |
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| DOID:0111691 | familial adult myoclonic epilepsy 5 | HGNC:2172 | Homo sapiens (human) | 6900 | CNTN2 |
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| DOID:0070258 | congenital disorder of glycosylation type IIf | HGNC:11021 | Homo sapiens (human) | 10559 | SLC35A1 |
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| DOID:576 | proteinuria | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:1240 | leukemia | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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| DOID:10652 | Alzheimer's disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:3407 | carotid artery disease | HGNC:12518 | Homo sapiens (human) | 7351 | UCP2 |
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| DOID:612 | primary immunodeficiency disease | HGNC:8086 | Homo sapiens (human) | 4938 | OAS1 |
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| DOID:0110178 | Charcot-Marie-Tooth disease axonal type 2V | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:0080199 | colorectal carcinoma | HGNC:6919 | Homo sapiens (human) | 8930 | MBD4 |
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| DOID:0111910 | spermatogenic failure | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:11162 | respiratory failure | HGNC:6922 | Homo sapiens (human) | 4153 | MBL2 |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | HGNC:19139 | Homo sapiens (human) | 55624 | POMGNT1 |
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| DOID:409 | liver disease | HGNC:9411 | Homo sapiens (human) | 5589 | PRKCSH |
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| DOID:10652 | Alzheimer's disease | HGNC:2911 | Homo sapiens (human) | 1743 | DLST |
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| DOID:0080555 | congenital disorder of glycosylation Ic | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8808 | Homo sapiens (human) | 5162 | PDHB |
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| DOID:0111898 | CK syndrome | HGNC:13398 | Homo sapiens (human) | 50814 | NSDHL |
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| DOID:440 | neuromuscular disease | HGNC:4458 | Homo sapiens (human) | 2821 | GPI |
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