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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:850 | lung disease | HGNC:10802 | Homo sapiens (human) | 6440 | SFTPC |
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| DOID:8947 | diabetic retinopathy | RGD:2915 | Rattus norvegicus (Norway rat) | 24505 | Ins1 |
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| DOID:678 | progressive supranuclear palsy | FB:FBgn0027864 | Drosophila melanogaster (fruit fly) | 31806 | Ogg1 |
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| DOID:13276 | Mycoplasma pneumoniae pneumonia | Xenbase:XB-GENE-1000113 | Xenopus laevis (African clawed frog) | 446948 | galc.L |
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| DOID:3307 | teratoma | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:418 | systemic scleroderma | SGD:S000002779 | Saccharomyces cerevisiae S288C | 851977 | CTS2 |
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| DOID:2377 | multiple sclerosis | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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| DOID:2211 | factor XIII deficiency | HGNC:6631 | Homo sapiens (human) | 3998 | LMAN1 |
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| DOID:3083 | chronic obstructive pulmonary disease | MGI:109521 | Mus musculus (house mouse) | 15558 | Htr2a |
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| DOID:589 | congenital hemolytic anemia | SGD:S000000400 | Saccharomyces cerevisiae S288C | 852495 | PGI1 |
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| DOID:0050700 | cardiomyopathy | HGNC:10680 | Homo sapiens (human) | 6389 | SDHA |
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| DOID:0110790 | hereditary spastic paraplegia 39 | HGNC:16268 | Homo sapiens (human) | 10908 | PNPLA6 |
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| DOID:1612 | breast cancer | WB:WBGene00000503 | Caenorhabditis elegans | 180628 | cht-1 |
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| DOID:11963 | esophagitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:13530 | Homo sapiens (human) | 10329 | RXYLT1 |
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| DOID:14067 | Plasmodium falciparum malaria | ZFIN:ZDB-GENE-060531-59 | Danio rerio (zebrafish) | 100005565 | gbgt1l8 |
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| DOID:0050424 | familial adenomatous polyposis | RGD:620045 | Rattus norvegicus (Norway rat) | 170841 | Mutyh |
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| DOID:0080561 | congenital disorder of glycosylation Ii | HGNC:23159 | Homo sapiens (human) | 85365 | ALG2 |
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| DOID:0110274 | autosomal recessive limb-girdle muscular dystrophy | ZFIN:ZDB-GENE-070112-1002 | Danio rerio (zebrafish) | 563878 | pomt2 |
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| DOID:1184 | nephrotic syndrome | HGNC:24865 | Homo sapiens (human) | 57678 | GPAM |
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| DOID:0060074 | ductal carcinoma in situ | MGI:1920212 | Mus musculus (house mouse) | 72962 | Tymp |
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| DOID:0050439 | Usher syndrome | HGNC:24102 | Homo sapiens (human) | 22901 | ARSG |
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| DOID:162 | cancer | FB:FBgn0026597 | Drosophila melanogaster (fruit fly) | 43565 | Axn |
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| DOID:10754 | otitis media | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:6364 | migraine | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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