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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:1214 | tympanosclerosis | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:10754 | otitis media | HGNC:3356 | Homo sapiens (human) | 5167 | ENPP1 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8808 | Homo sapiens (human) | 5162 | PDHB |
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| DOID:0014667 | disease of metabolism | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:0111910 | spermatogenic failure | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:8466 | retinal degeneration | HGNC:8807 | Homo sapiens (human) | 5161 | PDHA2 |
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| DOID:0080140 | multiple congenital anomalies-hypotonia-seizures syndrome 3 | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0060284 | paroxysmal nocturnal hemoglobinuria | HGNC:14938 | Homo sapiens (human) | 51604 | PIGT |
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| DOID:0014667 | disease of metabolism | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:3649 | pyruvate decarboxylase deficiency | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:8466 | retinal degeneration | HGNC:8806 | Homo sapiens (human) | 5160 | PDHA1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:224 | transient cerebral ischemia | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:3911 | progeria | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:9970 | obesity | HGNC:14934 | Homo sapiens (human) | 51548 | SIRT6 |
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| DOID:11612 | polycystic ovary syndrome | HGNC:5215 | Homo sapiens (human) | 51478 | HSD17B7 |
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| DOID:1701 | steroid inherited metabolic disorder | HGNC:5215 | Homo sapiens (human) | 51478 | HSD17B7 |
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| DOID:14227 | azoospermia | HGNC:29821 | Homo sapiens (human) | 51477 | ISYNA1 |
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| DOID:384 | Wolff-Parkinson-White syndrome | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:2747 | glycogen storage disease | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0110312 | hypertrophic cardiomyopathy 6 | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0090101 | lethal congenital glycogen storage disease of heart | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:1289 | neurodegenerative disease | HGNC:9386 | Homo sapiens (human) | 51422 | PRKAG2 |
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| DOID:0050585 | congenital generalized lipodystrophy | HGNC:8754 | Homo sapiens (human) | 5130 | PCYT1A |
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