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GlyTouCan
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
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
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:0112332 | pontocerebellar hypoplasia type 13 | HGNC:1172 | Homo sapiens (human) | 738 | VPS51 |
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| DOID:9620 | vesicoureteral reflux | HGNC:12580 | Homo sapiens (human) | 7380 | UPK3A |
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| DOID:10652 | Alzheimer's disease | HGNC:12585 | Homo sapiens (human) | 7384 | UQCRC1 |
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| DOID:0060892 | late onset Parkinson's disease | HGNC:12585 | Homo sapiens (human) | 7384 | UQCRC1 |
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| DOID:0070332 | multiple mitochondrial dysfunctions syndrome 6 | HGNC:12585 | Homo sapiens (human) | 7384 | UQCRC1 |
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| DOID:0080114 | mitochondrial complex III deficiency nuclear type 5 | HGNC:12586 | Homo sapiens (human) | 7385 | UQCRC2 |
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| DOID:0060399 | chromosome 16p12.1 deletion syndrome | HGNC:12586 | Homo sapiens (human) | 7385 | UQCRC2 |
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| DOID:0111139 | mitochondrial complex III deficiency | HGNC:12587 | Homo sapiens (human) | 7386 | UQCRFS1 |
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| DOID:700 | mitochondrial metabolism disease | HGNC:12587 | Homo sapiens (human) | 7386 | UQCRFS1 |
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| DOID:13270 | erythropoietic protoporphyria | HGNC:12592 | Homo sapiens (human) | 7390 | UROS |
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| DOID:13271 | cutaneous porphyria | HGNC:12592 | Homo sapiens (human) | 7390 | UROS |
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| DOID:0050439 | Usher syndrome | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0110360 | retinitis pigmentosa 39 | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0110827 | Usher syndrome type 2 | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0110838 | Usher syndrome type 2A | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:10584 | retinitis pigmentosa | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0050563 | nonsyndromic deafness | HGNC:12601 | Homo sapiens (human) | 7399 | USH2A |
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| DOID:0111438 | optic atrophy 5 | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:0070347 | encephalopathy due to defective mitochondrial and peroxisomal fission 1 | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:12930 | dilated cardiomyopathy | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:10652 | Alzheimer's disease | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:9352 | type 2 diabetes mellitus | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:14330 | Parkinson's disease | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:3770 | pulmonary fibrosis | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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| DOID:13711 | dental fluorosis | MGI:1921256 | Mus musculus (house mouse) | 74006 | Dnm1l |
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