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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:13271 | cutaneous porphyria | HGNC:12592 | Homo sapiens (human) | 7390 | UROS |
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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: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: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:9620 | vesicoureteral reflux | HGNC:12580 | Homo sapiens (human) | 7380 | UPK3A |
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| DOID:3525 | middle cerebral artery infarction | HGNC:12576 | Homo sapiens (human) | 7378 | UPP1 |
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| DOID:11702 | dysgammaglobulinemia | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:0060759 | immunodeficiency with hyper IgM type 5 | HGNC:12572 | Homo sapiens (human) | 7374 | UNG |
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| DOID:1574 | alcohol use disorder | HGNC:12566 | Homo sapiens (human) | 10497 | UNC13B |
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| DOID:1826 | epilepsy | HGNC:12566 | Homo sapiens (human) | 10497 | UNC13B |
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| DOID:0050833 | orotic aciduria | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:653 | purine-pyrimidine metabolic disorder | HGNC:12563 | Homo sapiens (human) | 7372 | UMPS |
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| DOID:1793 | pancreatic cancer | HGNC:12562 | Homo sapiens (human) | 7371 | UCK2 |
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| DOID:0060062 | familial juvenile hyperuricemic nephropathy | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:557 | kidney disease | HGNC:12559 | Homo sapiens (human) | 7369 | UMOD |
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| DOID:0080178 | mucositis | HGNC:12558 | Homo sapiens (human) | 8408 | ULK1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12541 | Homo sapiens (human) | 54600 | UGT1A9 |
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| DOID:4947 | cholangiocarcinoma | HGNC:12541 | Homo sapiens (human) | 54600 | UGT1A9 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12540 | Homo sapiens (human) | 54576 | UGT1A8 |
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| DOID:1793 | pancreatic cancer | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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