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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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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 | July 29, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▲ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:2945 | severe acute respiratory syndrome | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:13406 | pulmonary sarcoidosis | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:2841 | asthma | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:1793 | pancreatic cancer | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:14067 | Plasmodium falciparum malaria | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:0080600 | COVID-19 | HGNC:79 | Homo sapiens (human) | 28 | ABO |
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| DOID:9452 | steatotic liver disease | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
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| DOID:0080000 | muscular disease | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:84 | Homo sapiens (human) | 31 | ACACA |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
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| DOID:9452 | steatotic liver disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
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| DOID:0080000 | muscular disease | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
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| DOID:9970 | obesity | HGNC:85 | Homo sapiens (human) | 32 | ACACB |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0112072 | nuclear type mitochondrial complex I deficiency 20 | HGNC:88 | Homo sapiens (human) | 33 | ACADL |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
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| DOID:0080153 | medium chain acyl-CoA dehydrogenase deficiency | HGNC:89 | Homo sapiens (human) | 34 | ACADM |
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| DOID:1574 | alcohol use disorder | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:0080154 | short chain acyl-CoA dehydrogenase deficiency | HGNC:90 | Homo sapiens (human) | 35 | ACADS |
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| DOID:10652 | Alzheimer's disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080155 | very long chain acyl-CoA dehydrogenase deficiency | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:92 | Homo sapiens (human) | 37 | ACADVL |
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| DOID:8398 | osteoarthritis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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| DOID:2377 | multiple sclerosis | HGNC:319 | Homo sapiens (human) | 176 | ACAN |
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