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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:0060898 | Parkinson's disease 20 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0080464 | developmental and epileptic encephalopathy 53 | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:14330 | Parkinson's disease | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0060894 | early-onset Parkinson's disease | HGNC:11503 | Homo sapiens (human) | 8867 | SYNJ1 |
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| DOID:0060894 | early-onset Parkinson's disease | HGNC:11504 | Homo sapiens (human) | 8871 | SYNJ2 |
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| DOID:14330 | Parkinson's disease | HGNC:11504 | Homo sapiens (human) | 8871 | SYNJ2 |
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| DOID:14250 | Down syndrome | HGNC:11504 | Homo sapiens (human) | 8871 | SYNJ2 |
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| DOID:2978 | carbohydrate metabolic disorder | HGNC:11559 | Homo sapiens (human) | 6888 | TALDO1 |
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| DOID:10763 | hypertension | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:3526 | cerebral infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0060903 | thrombosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0112251 | Ghosal hematodiaphyseal syndrome | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:3454 | brain infarction | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:10976 | membranous glomerulonephritis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:11111 | hydronephrosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:0080998 | acute necrotizing pancreatitis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:2349 | arteriosclerosis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:9477 | pulmonary embolism | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:2921 | glomerulonephritis | HGNC:11609 | Homo sapiens (human) | 6916 | TBXAS1 |
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| DOID:13268 | porphyria | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:0080208 | metabolic dysfunction-associated steatotic liver disease | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:1724 | duodenal ulcer | HGNC:117 | Homo sapiens (human) | 48 | ACO1 |
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| DOID:0110544 | autosomal dominant nonsyndromic deafness 12 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:10003 | sensorineural hearing loss | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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| DOID:0110479 | autosomal recessive nonsyndromic deafness 21 | HGNC:11720 | Homo sapiens (human) | 7007 | TECTA |
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