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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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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:162 | cancer | SGD:S000001518 | Saccharomyces cerevisiae S288C | 853830 | UGP1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000006148 | Saccharomyces cerevisiae S288C | 855874 | ALG5 |
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| DOID:5212 | congenital disorder of glycosylation | SGD:S000000178 | Saccharomyces cerevisiae S288C | 852196 | ALG3 |
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| DOID:2747 | glycogen storage disease | SGD:S000004818 | Saccharomyces cerevisiae S288C | 855245 | PFK2 |
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| DOID:1588 | thrombocytopenia | SGD:S000000223 | Saccharomyces cerevisiae S288C | 852307 | GAL10 |
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| DOID:0050709 | early infantile epileptic encephalopathy | SGD:S000004982 | Saccharomyces cerevisiae S288C | 855691 | IDH1 |
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| DOID:2747 | glycogen storage disease | SGD:S000003472 | Saccharomyces cerevisiae S288C | 853155 | PFK1 |
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| DOID:0050570 | congenital disorder of glycosylation type I | SGD:S000000314 | Saccharomyces cerevisiae S288C | 852407 | ALG1 |
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| DOID:3429 | inclusion body myositis | HGNC:2666 | Homo sapiens (human) | 1605 | DAG1 |
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| DOID:1380 | endometrial cancer | HGNC:8977 | Homo sapiens (human) | 5293 | PIK3CD |
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| DOID:1682 | congenital heart disease | HGNC:4555 | Homo sapiens (human) | 2878 | GPX3 |
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| DOID:3070 | high grade glioma | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:576 | proteinuria | RGD:3001 | Rattus norvegicus (Norway rat) | 24536 | Lepr |
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| DOID:8893 | psoriasis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:2355 | anemia | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:1612 | breast cancer | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:10763 | hypertension | HGNC:2634 | Homo sapiens (human) | 1573 | CYP2J2 |
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| DOID:11151 | cholecystolithiasis | HGNC:12530 | Homo sapiens (human) | 54658 | UGT1A1 |
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| DOID:9351 | diabetes mellitus | HGNC:6257 | Homo sapiens (human) | 3767 | KCNJ11 |
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| DOID:2247 | spondylosis | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:10534 | stomach cancer | HGNC:4553 | Homo sapiens (human) | 2876 | GPX1 |
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| DOID:0081419 | childhood-onset dystonia with optic atrophy and basal ganglia abnormalities | HGNC:19691 | Homo sapiens (human) | 51102 | MECR |
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| DOID:5082 | liver cirrhosis | HGNC:8931 | Homo sapiens (human) | 5261 | PHKG2 |
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| DOID:676 | juvenile rheumatoid arthritis | HGNC:26789 | Homo sapiens (human) | 144811 | LACC1 |
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