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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:0050754 | ataxia with oculomotor apraxia type 1 | HGNC:15984 | Homo sapiens (human) | 54840 | APTX |
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| DOID:684 | hepatocellular carcinoma | SGD:S000002849 | Saccharomyces cerevisiae S288C | 852051 | APT2 |
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| DOID:1919 | Lesch-Nyhan syndrome | SGD:S000002849 | Saccharomyces cerevisiae S288C | 852051 | APT2 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | SGD:S000002849 | Saccharomyces cerevisiae S288C | 852051 | APT2 |
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | SGD:S000004484 | Saccharomyces cerevisiae S288C | 854986 | APT1 |
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| DOID:1919 | Lesch-Nyhan syndrome | SGD:S000004484 | Saccharomyces cerevisiae S288C | 854986 | APT1 |
|
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| DOID:684 | hepatocellular carcinoma | SGD:S000004484 | Saccharomyces cerevisiae S288C | 854986 | APT1 |
|
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| DOID:0060350 | adenine phosphoribosyltransferase deficiency | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:684 | hepatocellular carcinoma | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:1919 | Lesch-Nyhan syndrome | HGNC:626 | Homo sapiens (human) | 353 | APRT |
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| DOID:0111111 | maturity-onset diabetes of the young type 14 | HGNC:24035 | Homo sapiens (human) | 26060 | APPL1 |
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| DOID:0081292 | traumatic brain injury | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:0050850 | diabetic encephalopathy | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:9970 | obesity | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:0080348 | Alzheimer's disease 1 | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:824 | periodontitis | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:11758 | iron deficiency anemia | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:10652 | Alzheimer's disease | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:1561 | cognitive disorder | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:0070028 | APP-related cerebral amyloid angiopathy | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:10763 | hypertension | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:11832 | visual epilepsy | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:3525 | middle cerebral artery infarction | HGNC:620 | Homo sapiens (human) | 351 | APP |
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| DOID:225 | syndrome | HGNC:28727 | Homo sapiens (human) | 79135 | APOO |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:13916 | Homo sapiens (human) | 55937 | APOM |
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