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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:2527 | nephrosis | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:10652 | Alzheimer's disease | HGNC:9060 | Homo sapiens (human) | 5333 | PLCD1 |
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| DOID:4586 | familial meningioma | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0080547 | metabolic dysfunction-associated steatohepatitis | HGNC:2328 | Homo sapiens (human) | 1374 | CPT1A |
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| DOID:10907 | microcephaly | HGNC:1938 | Homo sapiens (human) | 1120 | CHKB |
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| DOID:12554 | hemolytic-uremic syndrome | HGNC:24338 | Homo sapiens (human) | 29071 | C1GALT1C1 |
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| DOID:2048 | autoimmune hepatitis | HGNC:11892 | Homo sapiens (human) | 7124 | TNF |
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| DOID:11949 | Creutzfeldt-Jakob disease | HGNC:9605 | Homo sapiens (human) | 5743 | PTGS2 |
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| DOID:1287 | cardiovascular system disease | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:2893 | cervix carcinoma | HGNC:587 | Homo sapiens (human) | 328 | APEX1 |
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| DOID:9111 | cutaneous leishmaniasis | HGNC:1516 | Homo sapiens (human) | 847 | CAT |
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| DOID:10283 | prostate cancer | HGNC:9588 | Homo sapiens (human) | 5728 | PTEN |
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| DOID:0050731 | vitamin B12 deficiency | HGNC:4013 | Homo sapiens (human) | 2524 | FUT2 |
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| DOID:4195 | hyperglycemia | HGNC:6107 | Homo sapiens (human) | 3651 | PDX1 |
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| DOID:83 | cataract | HGNC:4204 | Homo sapiens (human) | 2651 | GCNT2 |
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| DOID:3454 | brain infarction | HGNC:20580 | Homo sapiens (human) | 120227 | CYP2R1 |
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| DOID:0050560 | Walker-Warburg syndrome | HGNC:37276 | Homo sapiens (human) | 729920 | CRPPA |
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| DOID:1245 | vulva cancer | HGNC:391 | Homo sapiens (human) | 207 | AKT1 |
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| DOID:6432 | pulmonary hypertension | HGNC:435 | Homo sapiens (human) | 240 | ALOX5 |
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| DOID:0060041 | autism spectrum disorder | HGNC:3512 | Homo sapiens (human) | 2131 | EXT1 |
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| DOID:0080464 | developmental and epileptic encephalopathy 53 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:2349 | arteriosclerosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:6000 | congestive heart failure | HGNC:13633 | Homo sapiens (human) | 9370 | ADIPOQ |
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| DOID:3770 | pulmonary fibrosis | HGNC:5988 | Homo sapiens (human) | 8809 | IL18R1 |
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| DOID:4988 | alcoholic pancreatitis | HGNC:12539 | Homo sapiens (human) | 54577 | UGT1A7 |
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