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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:3393 | coronary artery disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:1074 | kidney failure | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:3525 | middle cerebral artery infarction | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:6432 | pulmonary hypertension | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:224 | transient cerebral ischemia | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:9970 | obesity | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:824 | periodontitis | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0112376 | muscular dystrophy-dystroglycanopathy type B15 | HGNC:3007 | Homo sapiens (human) | 54344 | DPM3 |
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| DOID:0080571 | congenital disorder of glycosylation Iu | HGNC:3006 | Homo sapiens (human) | 8818 | DPM2 |
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| DOID:0050570 | congenital disorder of glycosylation type I | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:0080557 | congenital disorder of glycosylation Ie | HGNC:3005 | Homo sapiens (human) | 8813 | DPM1 |
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| DOID:687 | hepatoblastoma | HGNC:3002 | Homo sapiens (human) | 1800 | DPEP1 |
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| DOID:0110676 | congenital myasthenic syndrome 13 | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:14227 | azoospermia | HGNC:29821 | Homo sapiens (human) | 51477 | ISYNA1 |
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| DOID:11396 | pulmonary edema | HGNC:29799 | Homo sapiens (human) | 259230 | SGMS1 |
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| DOID:0080070 | mucolipidosis II alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080071 | mucolipidosis III alpha/beta | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:0080488 | mucolipidosis | HGNC:29670 | Homo sapiens (human) | 79158 | GNPTAB |
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| DOID:5723 | optic atrophy | HGNC:29622 | Homo sapiens (human) | 27349 | MCAT |
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| DOID:11446 | sciatic neuropathy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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| DOID:11832 | visual epilepsy | HGNC:29595 | Homo sapiens (human) | 130120 | REG3G |
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