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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
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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:3650 | lactic acidosis | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2747 | glycogen storage disease | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:2754 | glycogen storage disease VI | HGNC:9725 | Homo sapiens (human) | 5836 | PYGL |
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| DOID:3651 | pyruvate carboxylase deficiency disease | SGD:S000000422 | Saccharomyces cerevisiae S288C | 852519 | PYC2 |
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| DOID:3651 | pyruvate carboxylase deficiency disease | SGD:S000003030 | Saccharomyces cerevisiae S288C | 852818 | PYC1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:4947 | cholangiocarcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:684 | hepatocellular carcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1824 | status epilepticus | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:3213 | demyelinating disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:332 | amyotrophic lateral sclerosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:12466 | secondary hyperparathyroidism | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:8634 | prostate carcinoma in situ | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1679 | cystitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:5394 | prolactinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:0080322 | polycystic kidney disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:5419 | schizophrenia | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:5082 | liver cirrhosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:6255 | growth hormone secreting pituitary adenoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:2349 | arteriosclerosis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:4029 | gastritis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:2999 | granulosa cell tumor | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:11963 | esophagitis | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:10652 | Alzheimer's disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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