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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:3525 | middle cerebral artery infarction | HGNC:4819 | Homo sapiens (human) | 3037 | HAS2 |
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| DOID:1936 | atherosclerosis | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:25812 | Homo sapiens (human) | 79644 | SRD5A3 |
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| DOID:3021 | acute kidney failure | HGNC:936 | Homo sapiens (human) | 572 | BAD |
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| DOID:0111933 | phosphoglycerate kinase 1 deficiency | HGNC:8896 | Homo sapiens (human) | 5230 | PGK1 |
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| DOID:5434 | scrapie | HGNC:9449 | Homo sapiens (human) | 5621 | PRNP |
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| DOID:3908 | lung non-small cell carcinoma | HGNC:5195 | Homo sapiens (human) | 9956 | HS3ST2 |
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| DOID:0081180 | autosomal recessive intellectual developmental disorder 12 | HGNC:10866 | Homo sapiens (human) | 6487 | ST3GAL3 |
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| DOID:1168 | familial hyperlipidemia | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:3393 | coronary artery disease | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:2018 | hyperinsulinism | HGNC:8872 | Homo sapiens (human) | 5207 | PFKFB1 |
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| DOID:1574 | alcohol use disorder | HGNC:13312 | Homo sapiens (human) | 9446 | GSTO1 |
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| DOID:684 | hepatocellular carcinoma | HGNC:8574 | Homo sapiens (human) | 5048 | PAFAH1B1 |
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| DOID:8577 | ulcerative colitis | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:0060001 | withdrawal disorder | HGNC:4092 | Homo sapiens (human) | 2571 | GAD1 |
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| DOID:12894 | Sjogren's syndrome | HGNC:1119 | Homo sapiens (human) | 684 | BST2 |
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| DOID:7148 | rheumatoid arthritis | HGNC:288 | Homo sapiens (human) | 155 | ADRB3 |
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| DOID:0050696 | fetal alcohol spectrum disorder | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:12716 | newborn respiratory distress syndrome | HGNC:10799 | Homo sapiens (human) | 729238 | SFTPA2 |
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| DOID:0080101 | Compton-North congenital myopathy | HGNC:2171 | Homo sapiens (human) | 1272 | CNTN1 |
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| DOID:12217 | Lewy body dementia | HGNC:8729 | Homo sapiens (human) | 5111 | PCNA |
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| DOID:0111042 | glycogen storage disease IXa | HGNC:8926 | Homo sapiens (human) | 5256 | PHKA2 |
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| DOID:0112343 | hereditary spastic paraplegia 82 | HGNC:8756 | Homo sapiens (human) | 5833 | PCYT2 |
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| DOID:1380 | endometrial cancer | HGNC:8905 | Homo sapiens (human) | 5236 | PGM1 |
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| DOID:557 | kidney disease | HGNC:6530 | Homo sapiens (human) | 3938 | LCT |
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