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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:8947 | diabetic retinopathy | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:381 | Homo sapiens (human) | 231 | AKR1B1 |
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| DOID:3910 | lung adenocarcinoma | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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| DOID:1612 | breast cancer | HGNC:380 | Homo sapiens (human) | 10327 | AKR1A1 |
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| DOID:0111670 | primary hyperoxaluria type 1 | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:2977 | primary hyperoxaluria | HGNC:341 | Homo sapiens (human) | 189 | AGXT |
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| DOID:0110657 | congenital myasthenic syndrome 8 | HGNC:329 | Homo sapiens (human) | 375790 | AGRN |
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| DOID:0110853 | rhizomelic chondrodysplasia punctata type 3 | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:2580 | rhizomelic chondrodysplasia punctata | HGNC:327 | Homo sapiens (human) | 8540 | AGPS |
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| DOID:811 | lipodystrophy | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0111135 | congenital generalized lipodystrophy type 1 | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:2748 | glycogen storage disease III | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:4676 | uremia | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:0110245 | cataract 38 | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:0080132 | Sengers syndrome | HGNC:21869 | Homo sapiens (human) | 55750 | AGK |
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| DOID:3211 | lysosomal storage disease | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:0050461 | aspartylglucosaminuria | HGNC:318 | Homo sapiens (human) | 175 | AGA |
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| DOID:13189 | gout | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:8947 | diabetic retinopathy | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:7148 | rheumatoid arthritis | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:9970 | obesity | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:10652 | Alzheimer's disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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