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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: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: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:0110474 | autosomal recessive nonsyndromic deafness 18B | HGNC:8516 | Homo sapiens (human) | 340990 | OTOG |
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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:5419 | schizophrenia | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:0060469 | Miller-Dieker lissencephaly syndrome | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:0050453 | lissencephaly | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| 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:0060058 | lymphoma | HGNC:8575 | Homo sapiens (human) | 5049 | PAFAH1B2 |
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| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
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| DOID:5154 | borna disease | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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| DOID:3454 | brain infarction | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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| DOID:0070352 | stress-induced childhood-onset neurodegeneration with variable ataxia and seizures | HGNC:8605 | Homo sapiens (human) | 8505 | PARG |
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