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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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Repository for lectin-assisted multimodality data
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MIRAGE
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 | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID ▼ | Species | Gene ID | Gene Symbol | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:684 | hepatocellular carcinoma | HGNC:14587 | Homo sapiens (human) | 54556 | ING3 |
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| DOID:1749 | squamous cell carcinoma | HGNC:14587 | Homo sapiens (human) | 54556 | ING3 |
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| DOID:162 | cancer | HGNC:14587 | Homo sapiens (human) | 54556 | ING3 |
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| DOID:0060937 | dystonia 30 | HGNC:14584 | Homo sapiens (human) | 64601 | VPS16 |
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| DOID:3211 | lysosomal storage disease | HGNC:14584 | Homo sapiens (human) | 64601 | VPS16 |
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| DOID:0060939 | dystonia 32 | HGNC:14583 | Homo sapiens (human) | 55823 | VPS11 |
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| DOID:0050987 | hypomyelinating leukoencephalopathy | HGNC:14583 | Homo sapiens (human) | 55823 | VPS11 |
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| DOID:0060796 | hypomyelinating leukodystrophy 12 | HGNC:14583 | Homo sapiens (human) | 55823 | VPS11 |
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| DOID:10487 | Hirschsprung's disease | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:0060894 | early-onset Parkinson's disease | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:0060369 | Parkinson's disease 6 | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:2998 | testicular cancer | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:0080855 | Parkinsonism | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:14330 | Parkinson's disease | HGNC:14581 | Homo sapiens (human) | 65018 | PINK1 |
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| DOID:0080199 | colorectal carcinoma | HGNC:1458 | Homo sapiens (human) | 813 | CALU |
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| DOID:13207 | proliferative diabetic retinopathy | HGNC:1458 | Homo sapiens (human) | 813 | CALU |
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| DOID:1682 | congenital heart disease | HGNC:14569 | Homo sapiens (human) | 51155 | JPT1 |
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| DOID:9970 | obesity | HGNC:14565 | Homo sapiens (human) | 10580 | SORBS1 |
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| DOID:9352 | type 2 diabetes mellitus | HGNC:14565 | Homo sapiens (human) | 10580 | SORBS1 |
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| DOID:13564 | aspergillosis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:2058 | chronic mucocutaneous candidiasis | HGNC:14558 | Homo sapiens (human) | 64581 | CLEC7A |
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| DOID:0111021 | cone-rod dystrophy 15 | HGNC:14550 | Homo sapiens (human) | 92211 | CDHR1 |
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| DOID:6000 | congestive heart failure | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:2394 | ovarian cancer | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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| DOID:8955 | sideroblastic anemia | HGNC:1455 | Homo sapiens (human) | 811 | CALR |
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