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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:10907 | microcephaly | HGNC:24649 | Homo sapiens (human) | 55500 | ETNK1 |
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| DOID:705 | Leber hereditary optic neuropathy | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0070519 | early-onset vitamin B6-dependent epilepsy 4 | HGNC:877 | Homo sapiens (human) | 501 | ALDH7A1 |
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| DOID:0080501 | GM1 gangliosidosis type 2 | HGNC:4298 | Homo sapiens (human) | 2720 | GLB1 |
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| DOID:4621 | holoprosencephaly | HGNC:8967 | Homo sapiens (human) | 23556 | PIGN |
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| DOID:10534 | stomach cancer | HGNC:19233 | Homo sapiens (human) | 170384 | FUT11 |
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| DOID:4971 | myelofibrosis | HGNC:11998 | Homo sapiens (human) | 7157 | TP53 |
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| DOID:0050866 | oral squamous cell carcinoma | HGNC:4141 | Homo sapiens (human) | 2597 | GAPDH |
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| DOID:10763 | hypertension | HGNC:7956 | Homo sapiens (human) | 4886 | NPY1R |
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| DOID:9675 | pulmonary emphysema | HGNC:6344 | Homo sapiens (human) | 9365 | KL |
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| DOID:5419 | schizophrenia | HGNC:5293 | Homo sapiens (human) | 3356 | HTR2A |
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| DOID:9119 | acute myeloid leukemia | HGNC:2615 | Homo sapiens (human) | 1555 | CYP2B6 |
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| DOID:0070433 | hyperphosphatasia with impaired intellectual development syndrome 1 | HGNC:26031 | Homo sapiens (human) | 55650 | PIGV |
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| DOID:14330 | Parkinson's disease | HGNC:9377 | Homo sapiens (human) | 5563 | PRKAA2 |
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| DOID:7693 | abdominal aortic aneurysm | HGNC:9040 | Homo sapiens (human) | 7941 | PLA2G7 |
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| DOID:0060856 | right atrial isomerism | HGNC:18292 | Homo sapiens (human) | 55997 | CFC1 |
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| DOID:1074 | kidney failure | HGNC:9237 | Homo sapiens (human) | 10891 | PPARGC1A |
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| DOID:0111061 | familial hypobetalipoproteinemia 2 | HGNC:491 | Homo sapiens (human) | 27329 | ANGPTL3 |
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| DOID:988 | mitral valve prolapse | HGNC:2707 | Homo sapiens (human) | 1636 | ACE |
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| DOID:9952 | acute lymphoblastic leukemia | HGNC:4922 | Homo sapiens (human) | 3098 | HK1 |
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| DOID:1852 | intrahepatic cholestasis | HGNC:18324 | Homo sapiens (human) | 80270 | HSD3B7 |
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| DOID:0090139 | cortisone reductase deficiency | HGNC:5208 | Homo sapiens (human) | 3290 | HSD11B1 |
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| DOID:6432 | pulmonary hypertension | HGNC:5344 | Homo sapiens (human) | 3383 | ICAM1 |
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| DOID:11335 | sarcoidosis | HGNC:1628 | Homo sapiens (human) | 929 | CD14 |
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| DOID:9744 | type 1 diabetes mellitus | HGNC:10720 | Homo sapiens (human) | 6402 | SELL |
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