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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:1826 | epilepsy | RGD:2168 | Rattus norvegicus (Norway rat) | 24212 | Atp1a2 |
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| DOID:4194 | glucose metabolism disease | MGI:2384910 | Mus musculus (house mouse) | 216019 | Hkdc1 |
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| DOID:9970 | obesity | RGD:62387 | Rattus norvegicus (Norway rat) | 29535 | Pdx1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:10659 | Homo sapiens (human) | 6383 | SDC2 |
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| DOID:10908 | hydrocephalus | HGNC:15505 | Homo sapiens (human) | 79143 | MBOAT7 |
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| DOID:0080139 | multiple congenital anomalies-hypotonia-seizures syndrome 2 | SGD:S000006096 | Saccharomyces cerevisiae S288C | 855928 | SPT14 |
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| DOID:12800 | mucopolysaccharidosis VI | HGNC:714 | Homo sapiens (human) | 411 | ARSB |
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| DOID:0060892 | late onset Parkinson's disease | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | Xenbase:XB-GENE-976628 | Xenopus laevis (African clawed frog) | 734516 | dpm1.S |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:2653 | Homo sapiens (human) | 1582 | CYP8B1 |
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| DOID:8778 | Crohn's disease | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:2247 | spondylosis | RGD:620396 | Rattus norvegicus (Norway rat) | 83504 | Kl |
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| DOID:10591 | pre-eclampsia | MGI:97879 | Mus musculus (house mouse) | 19662 | Rbp4 |
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| DOID:11714 | gestational diabetes | RGD:2137 | Rattus norvegicus (Norway rat) | 25239 | Apod |
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| DOID:9884 | muscular dystrophy | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:0050776 | non-syndromic X-linked intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0060178 | familial hemiplegic migraine | HGNC:800 | Homo sapiens (human) | 477 | ATP1A2 |
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| DOID:1470 | major depressive disorder | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:10595 | Charcot-Marie-Tooth disease | HGNC:7449 | Homo sapiens (human) | 8776 | MTMR1 |
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| DOID:3910 | lung adenocarcinoma | RGD:3329 | Rattus norvegicus (Norway rat) | 25513 | Pik3r1 |
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| DOID:0080575 | Larsen-like syndrome B3GAT3 type | ZFIN:ZDB-GENE-020419-3 | Danio rerio (zebrafish) | 192334 | b3gat3 |
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| DOID:3525 | middle cerebral artery infarction | RGD:2802 | Rattus norvegicus (Norway rat) | 25459 | Hmgb1 |
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| DOID:1324 | lung cancer | SGD:S000004164 | Saccharomyces cerevisiae S288C | 850871 | IDP2 |
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| DOID:2747 | glycogen storage disease | RGD:620687 | Rattus norvegicus (Norway rat) | 64035 | Pygl |
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| DOID:3525 | middle cerebral artery infarction | FB:FBgn0027864 | Drosophila melanogaster (fruit fly) | 31806 | Ogg1 |
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