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GlyTouCan
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:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:404 | Homo sapiens (human) | 217 | ALDH2 |
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| DOID:0050773 | paraganglioma | HGNC:2911 | Homo sapiens (human) | 1743 | DLST |
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| DOID:0050861 | colorectal adenocarcinoma | HGNC:2602 | Homo sapiens (human) | 1591 | CYP24A1 |
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| DOID:1909 | melanoma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0081001 | Cowden syndrome 5 | HGNC:8975 | Homo sapiens (human) | 5290 | PIK3CA |
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| DOID:0060041 | autism spectrum disorder | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:10754 | otitis media | HGNC:7632 | Homo sapiens (human) | 4669 | NAGLU |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:2921 | glomerulonephritis | HGNC:433 | Homo sapiens (human) | 246 | ALOX15 |
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| DOID:0060319 | cardiac arrest | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:10787 | premature menopause | HGNC:16940 | Homo sapiens (human) | 84649 | DGAT2 |
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| DOID:11758 | iron deficiency anemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:1824 | status epilepticus | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:9675 | pulmonary emphysema | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:3021 | acute kidney failure | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0080250 | erythrokeratodermia variabilis et progressiva 4 | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:0050770 | polycystic liver disease | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:8466 | retinal degeneration | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:0111043 | glycogen storage disease IXc | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:10283 | prostate cancer | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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| DOID:3892 | insulinoma | HGNC:11006 | Homo sapiens (human) | 6514 | SLC2A2 |
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| DOID:9452 | steatotic liver disease | HGNC:6553 | Homo sapiens (human) | 3952 | LEP |
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| DOID:0050571 | congenital disorder of glycosylation type II | HGNC:18305 | Homo sapiens (human) | 10159 | ATP6AP2 |
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| DOID:614 | lymphopenia | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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