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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:1459 | hypothyroidism | Xenbase:XB-GENE-943160 | Xenopus tropicalis (tropical clawed frog) | 550067 | cs |
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| DOID:0050866 | oral squamous cell carcinoma | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:9281 | phenylketonuria | SGD:S000005185 | Saccharomyces cerevisiae S288C | 855480 | ZWF1 |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:0014667 | disease of metabolism | HGNC:932 | Homo sapiens (human) | 570 | BAAT |
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| DOID:0050908 | myelodysplastic syndrome | SGD:S000004164 | Saccharomyces cerevisiae S288C | 850871 | IDP2 |
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| DOID:9452 | steatotic liver disease | HGNC:2631 | Homo sapiens (human) | 1571 | CYP2E1 |
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| DOID:3070 | high grade glioma | HGNC:6563 | Homo sapiens (human) | 3958 | LGALS3 |
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| DOID:9256 | colorectal cancer | HGNC:4554 | Homo sapiens (human) | 2877 | GPX2 |
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| DOID:2043 | hepatitis B | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | MGI:1330238 | Mus musculus (house mouse) | 13481 | Dpm2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:18294 | Homo sapiens (human) | 56052 | ALG1 |
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| DOID:0111241 | congenital muscular dystrophy-dystroglycanopathy type A5 | RGD:1305852 | Rattus norvegicus (Norway rat) | 308390 | Fkrp |
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| DOID:1580 | diffuse scleroderma | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:0081427 | autosomal recessive distal hereditary motor neuronopathy 8 | SGD:S000004060 | Saccharomyces cerevisiae S288C | 850759 | XYL2 |
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| DOID:0111240 | congenital muscular dystrophy-dystroglycanopathy type A2 | ZFIN:ZDB-GENE-070112-1002 | Danio rerio (zebrafish) | 563878 | pomt2 |
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| DOID:0080762 | autosomal recessive limb-girdle muscular dystrophy type 2Z | ZFIN:ZDB-GENE-051120-24 | Danio rerio (zebrafish) | 641495 | poglut1 |
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| DOID:13141 | uveitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:12930 | dilated cardiomyopathy | SGD:S000005284 | Saccharomyces cerevisiae S288C | 855732 | CIT1 |
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| DOID:2957 | pulmonary tuberculosis | HGNC:11847 | Homo sapiens (human) | 7096 | TLR1 |
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| DOID:2237 | hepatitis | SGD:S000004525 | Saccharomyces cerevisiae S288C | 854942 | OGG1 |
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| DOID:4247 | coronary restenosis | MGI:97250 | Mus musculus (house mouse) | 17869 | Myc |
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| DOID:9452 | steatotic liver disease | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:3314 | angiomyolipoma | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:0080664 | diaphyseal medullary stenosis with malignant fibrous histiocytoma | HGNC:7413 | Homo sapiens (human) | 4507 | MTAP |
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