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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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Repository for lectin-assisted multimodality data
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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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol | FlyGlycoDB ▲ | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0050338 | primary bacterial infectious disease | RGD:3673 | Rattus norvegicus (Norway rat) | 29499 | Shh |
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| DOID:1432 | blindness | SGD:S000005875 | Saccharomyces cerevisiae S288C | 854530 | PUT4 |
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| DOID:14766 | renal agenesis | ZFIN:ZDB-GENE-010226-3 | Danio rerio (zebrafish) | 79377 | gfra1b |
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| DOID:1067 | open-angle glaucoma | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0050465 | Muir-Torre syndrome | HGNC:7127 | Homo sapiens (human) | 4292 | MLH1 |
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| DOID:1934 | dysostosis | WB:WBGene00000168 | Caenorhabditis elegans | 178759 | apx-1 |
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| DOID:12361 | Graves' disease | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:0081120 | Graves ophthalmopathy | MGI:96542 | Mus musculus (house mouse) | 16175 | Il1a |
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| DOID:10322 | berylliosis | Xenbase:XB-GENE-865765 | Xenopus laevis (African clawed frog) | 397778 | tgfb1.L |
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| DOID:0080422 | Dravet syndrome | HGNC:10590 | Homo sapiens (human) | 6328 | SCN3A |
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| DOID:1574 | alcohol use disorder | MGI:109272 | Mus musculus (house mouse) | 22354 | Vipr1 |
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| DOID:3907 | lung squamous cell carcinoma | HGNC:11063 | Homo sapiens (human) | 8140 | SLC7A5 |
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| DOID:9970 | obesity | WB:WBGene00000567 | Caenorhabditis elegans | 176390 | cnx-1 |
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| DOID:10763 | hypertension | RGD:3177 | Rattus norvegicus (Norway rat) | 24596 | Ngfr |
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| DOID:0050580 | hereditary lymphedema | RGD:621861 | Rattus norvegicus (Norway rat) | 89805 | Angpt2 |
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| DOID:11054 | urinary bladder cancer | HGNC:1383 | Homo sapiens (human) | 768 | CA9 |
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| DOID:0110497 | autosomal recessive nonsyndromic deafness 39 | HGNC:4893 | Homo sapiens (human) | 3082 | HGF |
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| DOID:9352 | type 2 diabetes mellitus | MGI:103178 | Mus musculus (house mouse) | 22339 | Vegfa |
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| DOID:10763 | hypertension | RGD:628678 | Rattus norvegicus (Norway rat) | 260320 | F7 |
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| DOID:3407 | carotid artery disease | RGD:3020 | Rattus norvegicus (Norway rat) | 25008 | Lta |
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| DOID:12930 | dilated cardiomyopathy | MGI:87938 | Mus musculus (house mouse) | 11555 | Adrb2 |
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| DOID:3908 | lung non-small cell carcinoma | MGI:95530 | Mus musculus (house mouse) | 14194 | Fh1 |
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| DOID:614 | lymphopenia | HGNC:2433 | Homo sapiens (human) | 1436 | CSF1R |
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| DOID:0080685 | aortic dissection | RGD:2556 | Rattus norvegicus (Norway rat) | 24338 | Ephb1 |
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| DOID:9455 | lipid storage disease | RGD:3423 | Rattus norvegicus (Norway rat) | 25524 | Psap |
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