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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:0112237 | lissencephaly 1 | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:11832 | visual epilepsy | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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| DOID:9970 | obesity | HGNC:8527 | Homo sapiens (human) | 5019 | OXCT1 |
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| DOID:0110474 | autosomal recessive nonsyndromic deafness 18B | HGNC:8516 | Homo sapiens (human) | 340990 | OTOG |
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| DOID:0112275 | developmental and epileptic encephalopathy 93 | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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| DOID:0070129 | autosomal recessive cutis laxa type IID | HGNC:851 | Homo sapiens (human) | 523 | ATP6V1A |
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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: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:2394 | ovarian cancer | HGNC:8143 | Homo sapiens (human) | 4978 | OPCML |
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| DOID:5844 | myocardial infarction | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:783 | end stage renal disease | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:9246 | cerebral amyloid angiopathy | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:3393 | coronary artery disease | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:10763 | hypertension | HGNC:8133 | Homo sapiens (human) | 4973 | OLR1 |
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| DOID:0080240 | non-syndromic X-linked intellectual disability 106 | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:9351 | diabetes mellitus | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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| DOID:1712 | aortic valve stenosis | HGNC:8127 | Homo sapiens (human) | 8473 | OGT |
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