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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:2154 | nephroblastoma | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
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| DOID:10652 | Alzheimer's disease | HGNC:8724 | Homo sapiens (human) | 5105 | PCK1 |
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| DOID:0112002 | immunodeficiency 47 | HGNC:868 | Homo sapiens (human) | 537 | ATP6AP1 |
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| DOID:14701 | propionic acidemia | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8654 | Homo sapiens (human) | 5096 | PCCB |
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| DOID:9252 | amino acid metabolic disorder | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:14701 | propionic acidemia | HGNC:8653 | Homo sapiens (human) | 5095 | PCCA |
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| DOID:114 | heart disease | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:3748 | esophagus squamous cell carcinoma | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:7148 | rheumatoid arthritis | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:684 | hepatocellular carcinoma | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:1612 | breast cancer | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:557 | kidney disease | HGNC:8638 | Homo sapiens (human) | 8850 | KAT2B |
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| DOID:3651 | pyruvate carboxylase deficiency disease | HGNC:8636 | Homo sapiens (human) | 5091 | PC |
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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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| DOID:0050812 | spondyloepimetaphyseal dysplasia, Pakistani type | HGNC:8604 | Homo sapiens (human) | 9060 | PAPSS2 |
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| DOID:0060058 | lymphoma | HGNC:8575 | Homo sapiens (human) | 5049 | PAFAH1B2 |
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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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