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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:0081292 | traumatic brain injury | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:0080108 | myoglobinuria | HGNC:13345 | Homo sapiens (human) | 23175 | LPIN1 |
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| DOID:0070253 | congenital disorder of glycosylation type IIa | FB:FBgn0039738 | Drosophila melanogaster (fruit fly) | 43563 | Mgat2 | CG7921 |
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| DOID:9146 | visceral leishmaniasis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:13544 | low tension glaucoma | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:2355 | anemia | MGI:104798 | Mus musculus (house mouse) | 21926 | Tnf |
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| DOID:0050908 | myelodysplastic syndrome | RGD:3889 | Rattus norvegicus (Norway rat) | 24842 | Tp53 |
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| DOID:0050559 | Fukuyama congenital muscular dystrophy | ZFIN:ZDB-GENE-070410-96 | Danio rerio (zebrafish) | 100006345 | fktn |
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| DOID:3635 | congenital myasthenic syndrome | HGNC:1912 | Homo sapiens (human) | 1103 | CHAT |
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| DOID:2739 | Gilbert syndrome | RGD:3935 | Rattus norvegicus (Norway rat) | 24861 | Ugt1a1 |
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| DOID:3454 | brain infarction | MGI:96434 | Mus musculus (house mouse) | 16002 | Igf2 |
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| DOID:0050560 | Walker-Warburg syndrome | MGI:2179507 | Mus musculus (house mouse) | 246179 | Fktn |
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| DOID:9261 | nasopharynx carcinoma | MGI:98834 | Mus musculus (house mouse) | 22059 | Trp53 |
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| DOID:0080552 | congenital disorder of glycosylation Ia | RGD:2870 | Rattus norvegicus (Norway rat) | 24483 | Igf2 |
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| DOID:10591 | pre-eclampsia | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:10952 | nephritis | RGD:2053 | Rattus norvegicus (Norway rat) | 25591 | Parp1 |
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| DOID:0110958 | Gaucher's disease type II | WB:WBGene00021160 | Caenorhabditis elegans | 177314 | gba-4 |
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| DOID:854 | collagen disease | MGI:1341296 | Mus musculus (house mouse) | 21899 | Tlr6 |
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| DOID:7148 | rheumatoid arthritis | HGNC:6021 | Homo sapiens (human) | 3572 | IL6ST |
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| DOID:1459 | hypothyroidism | WB:WBGene00000833 | Caenorhabditis elegans | 176437 | cts-1 |
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| DOID:10652 | Alzheimer's disease | WB:WBGene00016204 | Caenorhabditis elegans | 183000 | gsto-1 |
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| DOID:863 | nervous system disease | MGI:88107 | Mus musculus (house mouse) | 232975 | Atp1a3 |
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| DOID:0050565 | autosomal recessive nonsyndromic deafness | Xenbase:XB-GENE-6488174 | Xenopus laevis (African clawed frog) | 108708472 | tmtc4.L |
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| DOID:4988 | alcoholic pancreatitis | MGI:3576092 | Mus musculus (house mouse) | 394434 | Ugt1a9 |
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| DOID:0050802 | Ehlers-Danlos syndrome spondylodysplastic type 2 | Xenbase:XB-GENE-6488390 | Xenopus laevis (African clawed frog) | 108696563 | b3galt6.L |
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