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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:10763 | hypertension | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:11664 | nephrosclerosis | HGNC:9592 | Homo sapiens (human) | 5730 | PTGDS |
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| DOID:1059 | intellectual disability | HGNC:3571 | Homo sapiens (human) | 2182 | ACSL4 |
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| DOID:0050847 | sleep apnea | HGNC:6554 | Homo sapiens (human) | 3953 | LEPR |
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| DOID:0060001 | withdrawal disorder | HGNC:2228 | Homo sapiens (human) | 1312 | COMT |
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| DOID:5212 | congenital disorder of glycosylation | HGNC:924 | Homo sapiens (human) | 2683 | B4GALT1 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:5209 | Homo sapiens (human) | 3291 | HSD11B2 |
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| DOID:3393 | coronary artery disease | HGNC:6619 | Homo sapiens (human) | 3990 | LIPC |
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| DOID:1679 | cystitis | RGD:3876 | Rattus norvegicus (Norway rat) | 24835 | Tnf |
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| DOID:811 | lipodystrophy | HGNC:325 | Homo sapiens (human) | 10555 | AGPAT2 |
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| DOID:0060058 | lymphoma | HGNC:8575 | Homo sapiens (human) | 5049 | PAFAH1B2 |
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| DOID:9470 | bacterial meningitis | HGNC:1932 | Homo sapiens (human) | 1116 | CHI3L1 |
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| DOID:2999 | granulosa cell tumor | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:9351 | diabetes mellitus | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:2595 | Homo sapiens (human) | 1543 | CYP1A1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:8125 | Homo sapiens (human) | 4968 | OGG1 |
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| DOID:3534 | Lafora disease | MGI:1341085 | Mus musculus (house mouse) | 13853 | Epm2a |
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| DOID:3343 | glycoproteinosis | MGI:97305 | Mus musculus (house mouse) | 18010 | Neu1 |
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| DOID:3312 | bipolar disorder | SGD:S000005163 | Saccharomyces cerevisiae S288C | 855502 | ALG9 |
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| DOID:3770 | pulmonary fibrosis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:4947 | cholangiocarcinoma | HGNC:7656 | Homo sapiens (human) | 4684 | NCAM1 |
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| DOID:0110429 | dilated cardiomyopathy 1H | HGNC:2592 | Homo sapiens (human) | 1585 | CYP11B2 |
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| DOID:5844 | myocardial infarction | HGNC:9603 | Homo sapiens (human) | 5740 | PTGIS |
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| DOID:12577 | urethral obstruction | HGNC:2594 | Homo sapiens (human) | 1588 | CYP19A1 |
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| DOID:4914 | esophagus adenocarcinoma | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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