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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:8725 | vascular dementia | MGI:1861437 | Mus musculus (house mouse) | 56637 | Gsk3b |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000005593 | Saccharomyces cerevisiae S288C | 854233 | ALG8 |
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| DOID:0080573 | congenital disorder of glycosylation Ix | Xenbase:XB-GENE-969897 | Xenopus laevis (African clawed frog) | 100380973 | stt3b.S |
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| DOID:8778 | Crohn's disease | MGI:105095 | Mus musculus (house mouse) | 18654 | Pgf |
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| DOID:11758 | iron deficiency anemia | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0080600 | COVID-19 | Xenbase:XB-GENE-6488967 | Xenopus laevis (African clawed frog) | 108698211 | abo.2.L |
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| DOID:3146 | lipid metabolism disorder | RGD:3000 | Rattus norvegicus (Norway rat) | 25608 | Lep |
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| DOID:1824 | status epilepticus | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:9675 | pulmonary emphysema | HGNC:14240 | Homo sapiens (human) | 55512 | SMPD3 |
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| DOID:9266 | cystinuria | MGI:1195264 | Mus musculus (house mouse) | 20532 | Slc3a1 |
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| DOID:3021 | acute kidney failure | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:1891 | optic nerve disease | SGD:S000004295 | Saccharomyces cerevisiae S288C | 851013 | ACO1 |
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| DOID:2565 | macular corneal dystrophy | Xenbase:XB-GENE-960886 | Xenopus laevis (African clawed frog) | 444431 | chst6.L |
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| DOID:0080250 | erythrokeratodermia variabilis et progressiva 4 | HGNC:4021 | Homo sapiens (human) | 2531 | KDSR |
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| DOID:684 | hepatocellular carcinoma | FB:FBgn0000109 | Drosophila melanogaster (fruit fly) | 48224 | Aprt |
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| DOID:0060669 | cerebral cavernous malformation | RGD:620916 | Rattus norvegicus (Norway rat) | 170911 | Pik3ca |
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| DOID:3307 | teratoma | RGD:1305756 | Rattus norvegicus (Norway rat) | 315219 | Tymp |
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| DOID:0060041 | autism spectrum disorder | ZFIN:ZDB-GENE-090312-199 | Danio rerio (zebrafish) | 100317129 | ndst3 |
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| DOID:0110671 | congenital myasthenic syndrome 6 | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:3891 | placental insufficiency | MGI:102851 | Mus musculus (house mouse) | 18609 | Pdx1 |
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| DOID:0050770 | polycystic liver disease | HGNC:23161 | Homo sapiens (human) | 79053 | ALG8 |
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| DOID:13406 | pulmonary sarcoidosis | Xenbase:XB-GENE-17341092 | Xenopus laevis (African clawed frog) | 108698863 | abo.4.L |
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| DOID:8466 | retinal degeneration | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:0111043 | glycogen storage disease IXc | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:10283 | prostate cancer | HGNC:386 | Homo sapiens (human) | 8644 | AKR1C3 |
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