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GlyTouCan
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:0080562 | congenital disorder of glycosylation Ij | HGNC:2995 | Homo sapiens (human) | 1798 | DPAGT1 |
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| DOID:687 | hepatoblastoma | HGNC:3002 | Homo sapiens (human) | 1800 | DPEP1 |
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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: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: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:8893 | psoriasis | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| DOID:3407 | carotid artery disease | HGNC:30092 | Homo sapiens (human) | 10135 | NAMPT |
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| 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:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:162 | cancer | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:0080566 | congenital disorder of glycosylation In | HGNC:30220 | Homo sapiens (human) | 91869 | RFT1 |
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| DOID:10283 | prostate cancer | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:104 | bacterial infectious disease | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:0081183 | autosomal recessive intellectual developmental disorder 7 | HGNC:30242 | Homo sapiens (human) | 7991 | TUSC3 |
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| DOID:2377 | multiple sclerosis | HGNC:30308 | Homo sapiens (human) | 56963 | RGMA |
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