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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:0050560 | Walker-Warburg syndrome | RGD:620078 | Rattus norvegicus (Norway rat) | 84430 | Pomt1 |
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| DOID:898 | autosomal dominant polycystic kidney disease | HGNC:7155 | Homo sapiens (human) | 4312 | MMP1 |
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| DOID:3883 | Lynch syndrome | MGI:1915445 | Mus musculus (house mouse) | 100037283 | Rnaset2a |
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| DOID:0080555 | congenital disorder of glycosylation Ic | HGNC:23157 | Homo sapiens (human) | 29929 | ALG6 |
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| DOID:10591 | pre-eclampsia | HGNC:9650 | Homo sapiens (human) | 5771 | PTPN2 |
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| DOID:8677 | perinatal necrotizing enterocolitis | MGI:1932389 | Mus musculus (house mouse) | 81897 | Tlr9 |
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| DOID:0060041 | autism spectrum disorder | HGNC:21226 | Homo sapiens (human) | 57497 | LRFN2 |
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| DOID:326 | ischemia | ZFIN:ZDB-GENE-040513-5 | Danio rerio (zebrafish) | 407668 | asic4a |
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| DOID:0060180 | colitis | MGI:96211 | Mus musculus (house mouse) | 15439 | Hp |
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| DOID:11984 | hypertrophic cardiomyopathy | ZFIN:ZDB-GENE-050522-100 | Danio rerio (zebrafish) | 402892 | orai1b |
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| DOID:1920 | hyperuricemia | HGNC:6526 | Homo sapiens (human) | 3934 | LCN2 |
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| DOID:8947 | diabetic retinopathy | MGI:1921765 | Mus musculus (house mouse) | 68916 | Cdkal1 |
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| DOID:0081267 | graft-versus-host disease | Xenbase:XB-GENE-17341092 | Xenopus laevis (African clawed frog) | 108698863 | abo.4.L |
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| DOID:3393 | coronary artery disease | HGNC:8583 | Homo sapiens (human) | 5054 | SERPINE1 |
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| DOID:0060868 | leukoencephalopathy with vanishing white matter | HGNC:3260 | Homo sapiens (human) | 8890 | EIF2B4 |
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| DOID:1612 | breast cancer | HGNC:2910 | Homo sapiens (human) | 54567 | DLL4 |
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| DOID:0110739 | neurodegeneration with brain iron accumulation 5 | RGD:1359718 | Rattus norvegicus (Norway rat) | 302559 | Wdr45 |
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| DOID:9952 | acute lymphoblastic leukemia | WB:WBGene00003995 | Caenorhabditis elegans | 178215 | pgp-1 |
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| DOID:8778 | Crohn's disease | WB:WBGene00000054 | Caenorhabditis elegans | 191602 | acr-15 |
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| DOID:1059 | intellectual disability | HGNC:30313 | Homo sapiens (human) | 23352 | UBR4 |
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| DOID:3021 | acute kidney failure | HGNC:10963 | Homo sapiens (human) | 6580 | SLC22A1 |
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| DOID:1289 | neurodegenerative disease | ZFIN:ZDB-GENE-020416-3 | Danio rerio (zebrafish) | 192309 | tpi1a |
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| DOID:12387 | nephrogenic diabetes insipidus | WB:WBGene00011582 | Caenorhabditis elegans | 188227 | ntr-1 |
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| DOID:4724 | brain edema | MGI:1333777 | Mus musculus (house mouse) | 11828 | Aqp3 |
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| DOID:11716 | prediabetes syndrome | HGNC:1603 | Homo sapiens (human) | 729230 | CCR2 |
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