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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:4676 | uremia | HGNC:321 | Homo sapiens (human) | 178 | AGL |
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| DOID:9970 | obesity | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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| DOID:1273 | respiratory syncytial virus infectious disease | MGI:96824 | Mus musculus (house mouse) | 21898 | Tlr4 |
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| DOID:83 | cataract | HGNC:6708 | Homo sapiens (human) | 4047 | LSS |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | RGD:1589723 | Rattus norvegicus (Norway rat) | 363464 | Piga |
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| DOID:0112319 | Kanzaki disease | HGNC:7631 | Homo sapiens (human) | 4668 | NAGA |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:8947 | diabetic retinopathy | WB:WBGene00001685 | Caenorhabditis elegans | 180601 | gpd-3 |
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| DOID:2316 | brain ischemia | HGNC:6971 | Homo sapiens (human) | 4191 | MDH2 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | HGNC:7045 | Homo sapiens (human) | 4247 | MGAT2 |
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| DOID:0050453 | lissencephaly | SGD:S000003904 | Saccharomyces cerevisiae S288C | 853608 | PMT4 |
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| DOID:10652 | Alzheimer's disease | HGNC:6126 | Homo sapiens (human) | 8660 | IRS2 |
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| DOID:9952 | acute lymphoblastic leukemia | SGD:S000001949 | Saccharomyces cerevisiae S288C | 850614 | HXK1 |
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| DOID:6543 | acne | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10763 | hypertension | HGNC:6294 | Homo sapiens (human) | 3784 | KCNQ1 |
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| DOID:783 | end stage renal disease | RGD:628825 | Rattus norvegicus (Norway rat) | 85496 | Enpp1 |
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| DOID:0050453 | lissencephaly | Xenbase:XB-GENE-6489079 | Xenopus laevis (African clawed frog) | 108698684 | pomt2.L |
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| DOID:3803 | Crigler-Najjar syndrome | FB:FBgn0015663 | Drosophila melanogaster (fruit fly) | 44058 | Ugt36A1 |
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| DOID:1824 | status epilepticus | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:1070 | primary open angle glaucoma | SGD:S000004525 | Saccharomyces cerevisiae S288C | 854942 | OGG1 |
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| DOID:1459 | hypothyroidism | HGNC:11284 | Homo sapiens (human) | 6715 | SRD5A1 |
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| DOID:11984 | hypertrophic cardiomyopathy | SGD:S000000598 | Saccharomyces cerevisiae S288C | 850361 | CIT2 |
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| DOID:0060175 | succinic semialdehyde dehydrogenase deficiency | HGNC:408 | Homo sapiens (human) | 7915 | ALDH5A1 |
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| DOID:2861 | congenital nonspherocytic hemolytic anemia | SGD:S000005185 | Saccharomyces cerevisiae S288C | 855480 | ZWF1 |
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| DOID:2377 | multiple sclerosis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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