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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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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:824 | periodontitis | RGD:2802 | Rattus norvegicus (Norway rat) | 25459 | Hmgb1 |
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| DOID:0060413 | chromosome 22q11.2 deletion syndrome, distal | HGNC:10979 | Homo sapiens (human) | 6576 | SLC25A1 |
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| DOID:1070 | primary open angle glaucoma | MGI:96824 | Mus musculus (house mouse) | 21898 | Tlr4 |
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| DOID:0050588 | muscular dystrophy-dystroglycanopathy type B1 | Xenbase:XB-GENE-6250446 | Xenopus tropicalis (tropical clawed frog) | 100498555 | large1 |
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| DOID:9970 | obesity | HGNC:4057 | Homo sapiens (human) | 2539 | G6PD |
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| DOID:1074 | kidney failure | HGNC:11850 | Homo sapiens (human) | 7099 | TLR4 |
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| DOID:1289 | neurodegenerative disease | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:0050700 | cardiomyopathy | MGI:2138994 | Mus musculus (house mouse) | 99011 | Pomt1 |
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| DOID:14067 | Plasmodium falciparum malaria | RGD:628609 | Rattus norvegicus (Norway rat) | 65270 | Abo3 |
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| DOID:2747 | glycogen storage disease | SGD:S000004248 | Saccharomyces cerevisiae S288C | 850962 | GSY2 |
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| DOID:0111236 | congenital muscular dystrophy-dystroglycanopathy type A3 | Xenbase:XB-GENE-959859 | Xenopus laevis (African clawed frog) | 495292 | pomgnt1.S |
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| DOID:0110292 | autosomal recessive limb-girdle muscular dystrophy type 2O | Xenbase:XB-GENE-17345074 | Xenopus laevis (African clawed frog) | 414570 | pomgnt1.L |
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| DOID:0050745 | diffuse large B-cell lymphoma | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:1909 | melanoma | SGD:S000002779 | Saccharomyces cerevisiae S288C | 851977 | CTS2 |
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| DOID:12297 | Vogt-Koyanagi-Harada disease | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:936 | brain disease | SGD:S000001217 | Saccharomyces cerevisiae S288C | 856579 | ENO2 |
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| DOID:10273 | heart conduction disease | MGI:108083 | Mus musculus (house mouse) | 16535 | Kcnq1 |
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| DOID:0014667 | disease of metabolism | HGNC:21481 | Homo sapiens (human) | 92483 | LDHAL6B |
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| DOID:0110278 | autosomal recessive limb-girdle muscular dystrophy type 2D | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | MGI:1278315 | Mus musculus (house mouse) | 16973 | Lrp5 |
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| DOID:1380 | endometrial cancer | ZFIN:ZDB-GENE-040426-2762 | Danio rerio (zebrafish) | 406731 | ugt1ab |
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| DOID:1826 | epilepsy | HGNC:24649 | Homo sapiens (human) | 55500 | ETNK1 |
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| DOID:224 | transient cerebral ischemia | RGD:2645 | Rattus norvegicus (Norway rat) | 24377 | G6pd |
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| DOID:0080283 | developmental and epileptic encephalopathy 55 | HGNC:3046 | Homo sapiens (human) | 51227 | PIGP |
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| DOID:9296 | cleft lip | SGD:S000003904 | Saccharomyces cerevisiae S288C | 853608 | PMT4 |
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