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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:0050881 | inclusion body myopathy with Paget disease of bone and frontotemporal dementia | HGNC:3229 | Homo sapiens (human) | 1950 | EGF |
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| DOID:14227 | azoospermia | HGNC:7680 | Homo sapiens (human) | 3340 | NDST1 |
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| DOID:9296 | cleft lip | Xenbase:XB-GENE-6254666 | Xenopus laevis (African clawed frog) | 394283 | sdc2.S |
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| DOID:10892 | hypospadias | MGI:109392 | Mus musculus (house mouse) | 13983 | Esr2 |
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| DOID:0080440 | developmental and epileptic encephalopathy 3 | MGI:1915517 | Mus musculus (house mouse) | 68267 | Slc25a22 |
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| DOID:0060170 | generalized epilepsy with febrile seizures plus | HGNC:10597 | Homo sapiens (human) | 6335 | SCN9A |
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| DOID:7148 | rheumatoid arthritis | WB:WBGene00016283 | Caenorhabditis elegans | 178748 | zmp-3 |
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| DOID:4362 | cervical cancer | FB:FBgn0003731 | Drosophila melanogaster (fruit fly) | 37455 | Egfr |
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| DOID:5844 | myocardial infarction | HGNC:3180 | Homo sapiens (human) | 1910 | EDNRB |
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| DOID:1574 | alcohol use disorder | WB:WBGene00006783 | Caenorhabditis elegans | 176431 | unc-47 |
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| DOID:0080207 | CAKUT2 | RGD:621675 | Rattus norvegicus (Norway rat) | 116510 | Timp1 |
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| DOID:11832 | visual epilepsy | WB:WBGene00000857 | Caenorhabditis elegans | 173399 | cwn-1 |
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| DOID:3082 | interstitial lung disease | HGNC:10801 | Homo sapiens (human) | 6439 | SFTPB |
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| DOID:0060041 | autism spectrum disorder | FB:FBgn0028646 | Drosophila melanogaster (fruit fly) | 43616 | aralar1 |
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| DOID:0050848 | obstructive sleep apnea | MGI:96211 | Mus musculus (house mouse) | 15439 | Hp |
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| DOID:8947 | diabetic retinopathy | MGI:96572 | Mus musculus (house mouse) | 16333 | Ins1 |
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| DOID:1287 | cardiovascular system disease | RGD:620925 | Rattus norvegicus (Norway rat) | 83516 | Ppargc1a |
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| DOID:2030 | anxiety disorder | MGI:2444484 | Mus musculus (house mouse) | 242362 | Manea |
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| DOID:13025 | retinopathy of prematurity | MGI:96683 | Mus musculus (house mouse) | 16542 | Kdr |
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| DOID:13317 | hyperinsulinemic hypoglycemia | SGD:S000002924 | Saccharomyces cerevisiae S288C | 852128 | EMI2 |
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| DOID:0060823 | syndromic X-linked intellectual disability 94 | MGI:95810 | Mus musculus (house mouse) | 53623 | Gria3 |
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| DOID:0050770 | polycystic liver disease | WB:WBGene00018682 | Caenorhabditis elegans | 180400 | aagr-4 |
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| DOID:10126 | keratoconus | MGI:1316726 | Mus musculus (house mouse) | 14161 | Fga |
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| DOID:4448 | macular degeneration | MGI:97011 | Mus musculus (house mouse) | 17395 | Mmp9 |
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| DOID:0080056 | achondrogenesis type II | Xenbase:XB-GENE-6252613 | Xenopus laevis (African clawed frog) | 397738 | col2a1.L |
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